CD BioSciences Unveiled WMicroTrackers, Powered by Non-invasive Tracking Technology

CD BioSciences is proud to announce the launch of WMicroTrackers powered by non-invasive tracking technology to ensure more accurate and reliable data.

CD BioSciences, a leading provider of innovative biotechnology solutions, is proud to announce the launch of WMicroTrackers powered by non-invasive tracking technology to minimize stress and interference with the organisms, ensuring more accurate and reliable data.

“We are excited to introduce our WMicroTrackers to the scientific community,” said the marketing manager of CD BioSciences. “Our automated micro-tracker systems are designed to make your scientific research more convenient.”

WMicroTrackers from CD BioSciences are a cutting-edge solution that allows researchers and scientists to automatically track and monitor worm paths in real time without the need for invasive procedures. By utilizing cutting-edge imaging technology and flexible tracking algorithms, WMicroTrackers bring disruptive innovation in the measurement of compound toxicity, resistance to stress, search for new anthelmintics, metabolic, lifetime, and human disease models. These innovative systems represent a significant advancement in scientific research and have the potential to revolutionize how research is conducted in a wide range of fields.

So far, CD BioSciences offers four automated worm trackers including WMicrotracker ONE, WMicrotracker ARENA, WMicrotracker SMART, and WMicrotracker Mini. These systems have been validated for use in C.elegans and further optimized for measurements of animals cultured in a liquid, agar solid, or air medium by using different types of microplate formats. In general, the key features of the WMicroTrackers include

• High-resolution imaging capabilities

• Real-time monitoring of biological processes

• Non-invasive tracking technology

• User-friendly interface for easy data analysis and interpretation

At CD BioSciences, the company is committed to providing cutting-edge solutions that empower researchers and scientists to make groundbreaking discoveries. With the launch of its WMicroTrackers, the company continues to lead the way in innovation and technology in drug screening, mutant/RNAi screening, chemotaxis, neurodegeneration, developmental toxicology, health span and lifespan, and much more.

About CD BioSciences

CD BioSciences, located in New York, is a professional provider of C. elegans model services. With a focus on advancing technology and driving scientific discovery, the company is committed to providing the most reliable research services with comprehensive data analysis, faster turnaround time, and the most competitive prices. CD BioSciences’ services involve C. elegans genome editing, the construction of the C. elegans stress response model, aging research, drug screening, and C. elegans biology among others.

Media Contact
Company Name: CD BioSciences
Contact Person: Michelle Moser
Email: Send Email
Country: United States
Website: https://www.elegansmodel.com/

 

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FloodFix: A Port Charlotte Water Damage Restoration Company Making Customers Happy

FloodFix Water Damage Restoration, a leading provider of Port Charlotte water damage restoration services, is pleased to announce its expansion into Port Charlotte, Florida. The company is now available to serve homeowners and businesses in the Greater Port Charlotte area with its comprehensive suite of water damage restoration services.

24/7 Emergency Response for Water Damage

FloodFix Water Damage Restoration in Port Charlotte understands that water damage can be a devastating event, and that’s why they offer 24/7 emergency response services. Their team of experienced professionals is available to respond to your call immediately, regardless of the time of day or night.

Comprehensive Water Damage Restoration Services

FloodFix Water Damage Restoration offers a full range of water damage restoration services, including:

  • Water extraction and drying
  • Mold remediation
  • Structural repairs
  • Contents cleaning and restoration
  • Dehumidification


Committed to Customer Satisfaction

Committed to delivering exceptional service and customer satisfaction, FloodFix Water Damage Restoration recognizes the stress and overwhelm water damage can cause. Their aim is to ensure a smooth and hassle-free restoration experience for their clientele.

Serving the Port Charlotte Community

Standing firmly behind their commitment to the Port Charlotte community, FloodFix Water Damage Restoration prioritizes assisting homeowners and businesses in swift recovery from water damage, enabling them to return to normalcy as soon as possible.

If you are experiencing water damage in Port Charlotte, FL, call FloodFix Water Damage Restoration today at (941) 336-7896.

About FloodFix Water Damage Restoration

FloodFix Water Damage Restoration is a leading provider of water damage restoration services. The company has a team of experienced professionals who are available to respond to your emergency water damage needs 24/7. FloodFix Water Damage Restoration is committed to providing customers with the highest quality of service and satisfaction. See their reviews here

Business Information

FloodFix Water Damage Restoration
1825 TAMIAMI TRAIL STE J # 1091 PORT CHARLOTTE, FL 33948
(941) 336-7896
Port Charlotte Water Damage Restoration Service

Media Contact
Company Name: FloodFix Water Damage Restoration
Contact Person: Sydney Burke
Email: Send Email
City: Port Charlotte
State: Florida
Country: United States
Website: https://floodfixwaterdamagerestoration.com/port-charlotte/

 

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Severe Hypertriglyceridemia Market Report 2032: Epidemiology Data, Pipeline Therapies, Latest FDA, EMA, PDMA Approvals by DelveInsight | Ionis Pharma, 89bio, Inc., Arrowhead Pharma, Hightide

“Severe Hypertriglyceridemia Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Severe Hypertriglyceridemia, historical and forecasted epidemiology as well as the Severe Hypertriglyceridemia market trends in the 7MM.

DelveInsight’s “Severe Hypertriglyceridemia Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Severe Hypertriglyceridemia, historical and forecasted epidemiology as well as the Severe Hypertriglyceridemia market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.

 

To Know in detail about the Severe Hypertriglyceridemia market outlook, drug uptake, treatment scenario and epidemiology trends, Click here; Severe Hypertriglyceridemia Market Forecast

 

Some of the key facts of the Severe Hypertriglyceridemia Market Report: 

  • The Severe Hypertriglyceridemia market size was valued approximately USD 2,408 million in 2022 and is anticipated to grow with a significant CAGR during the study period (2019-2032)
  • In the 7MM, hypertriglyceridemia was detected in about 69,607,255 prevalent cases in 2022. Over the predicted period, a rise in these cases is anticipated
  • At a noteworthy CAGR during the study period (2019–2022), the total diagnosed prevalent cases of severe hypertriglyceridemia in the 7MM were reported to be 3,480,363 in 2022
  • With 364,734 cases diagnosed, Germany had the highest prevalence of SHTG among European nations in 2022. The UK came in second with 278,983 cases. Spain, on the other hand, had the lowest population with a diagnosis
  • Sixteen percent of the total cases of SHTG in the 7MM occurred in Japan in 2022, with 562,041 diagnosed prevalent cases
  • About 44% of all cases in the 7MM were seen to be diagnosed as prevalent cases of hypertriglyceridemia in the US in 2022. Over the research period, these cases are anticipated to increase at a notable CAGR (2019–2032).
  • Among the important assets in the SHTG pipeline are Olezarsen (ApoC-III), ARO-APOC3, and Pegozafermin (BIO89-100), among others. These assets, if launched successfully, will drive market expansion throughout the course of the projection period.
  • Key Severe Hypertriglyceridemia Companies: Ionis Pharmaceuticals, 89bio, Inc., Arrowhead Pharmaceuticals, Inc., Hightide Therapeutics, AstraZeneca, Kowa Research Institute, Inc., Regeneron Pharmaceuticals, Mochida Pharmaceutical, NeuroBo Pharma, Arisaph Pharma, Acasti Pharma Inc., and others
  • Key Severe Hypertriglyceridemia Therapies: Olezarsen, Pegozafermin (BIO89-100), ARO-APOC3, HTD1801, omefas, K-877, evinacumab, Ethyl Icosapentate, Gemcabene, ARI-3037MO, CaPre, Epanova, and others
  • The Severe Hypertriglyceridemia epidemiology based on gender analyzed that the severity‐specific data reveal the highest number of cases were observed in moderate level of HTG
  • The Severe Hypertriglyceridemia market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Severe Hypertriglyceridemia pipeline products will significantly revolutionize the Severe Hypertriglyceridemia market dynamics.

 

Severe Hypertriglyceridemia Overview

Primary illnesses and secondary disorders are the two basic categories into which severe hypertriglyceridemia falls. Genetic illnesses fall under the category of main disorders, with secondary causes and other underlying conditions frequently contributing to the latter.

 

Get a Free sample for the Severe Hypertriglyceridemia Market Report:

https://www.delveinsight.com/report-store/severe-hypertriglyceridemia-shtg-market

 

Severe Hypertriglyceridemia Epidemiology

The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2019 to 2032. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.

 

Severe Hypertriglyceridemia Epidemiology Segmentation:

The Severe Hypertriglyceridemia market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into:

  • Total Prevalence of Severe Hypertriglyceridemia
  • Prevalent Cases of Severe Hypertriglyceridemia by severity
  • Gender-specific Prevalence of Severe Hypertriglyceridemia
  • Diagnosed Cases of Episodic and Chronic Severe Hypertriglyceridemia

 

Download the report to understand which factors are driving Severe Hypertriglyceridemia epidemiology trends @ Severe Hypertriglyceridemia Epidemiology Forecast

 

Severe Hypertriglyceridemia Drugs Uptake and Pipeline Development Activities

The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Severe Hypertriglyceridemia market or expected to get launched during the study period. The analysis covers Severe Hypertriglyceridemia market uptake by drugs, patient uptake by therapies, and sales of each drug. 

Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.

The report also covers the Severe Hypertriglyceridemia Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.

 

Severe Hypertriglyceridemia Therapies and Key Companies

  • Olezarsen: Ionis Pharmaceuticals
  • Pegozafermin (BIO89-100): 89bio, Inc.
  • ARO-APOC3: Arrowhead Pharmaceuticals, Inc.
  • HTD1801: HightideTherapeutics
  • omefas: AstraZeneca
  • K-877: Kowa Research Institute, Inc.
  • evinacumab: Regeneron Pharmaceuticals
  • Ethyl Icosapentate: Mochida Pharmaceutical
  • Gemcabene: NeuroBo Pharma
  • ARI-3037MO: Arisaph Pharma
  • CaPre: Acasti Pharma Inc.
  • Epanova: AstraZeneca

 

Discover more about therapies set to grab major Severe Hypertriglyceridemia market share @ Severe Hypertriglyceridemia Treatment Market

 

Severe Hypertriglyceridemia Market Strengths

  • The increasing prevalent population and increasing episodes of primary and secondary causes worldwide are likely to cause a surge in treatment options. Consequently, the market will witness a boost in the upcoming year

 

Severe Hypertriglyceridemia Market Opportunities

  • Medications with better safety and effectiveness, which provide an optimum cure, are the current unmet need of the SHTG disease market.

 

Scope of the Severe Hypertriglyceridemia Market Report

  • Study Period: 2019–2032
  • Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
  • Key Severe Hypertriglyceridemia Companies: Ionis Pharmaceuticals, 89bio, Inc., Arrowhead Pharmaceuticals, Inc., Hightide Therapeutics, AstraZeneca, Kowa Research Institute, Inc., Regeneron Pharmaceuticals, Mochida Pharmaceutical, NeuroBo Pharma, Arisaph Pharma, Acasti Pharma Inc., and others
  • Key Severe Hypertriglyceridemia Therapies: Olezarsen, Pegozafermin (BIO89-100), ARO-APOC3, HTD1801, omefas, K-877, evinacumab, Ethyl Icosapentate, Gemcabene, ARI-3037MO, CaPre, Epanova, and others
  • Severe Hypertriglyceridemia Therapeutic Assessment: Severe Hypertriglyceridemia current marketed and Severe Hypertriglyceridemia emerging therapies
  • Severe Hypertriglyceridemia Market Dynamics: Severe Hypertriglyceridemia market drivers and Severe Hypertriglyceridemia market barriers 
  • Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Severe Hypertriglyceridemia Unmet Needs, KOL’s views, Analyst’s views, Severe Hypertriglyceridemia Market Access and Reimbursement 

 

To know more about Severe Hypertriglyceridemia companies working in the treatment market, visit @ Severe Hypertriglyceridemia Clinical Trials and Therapeutic Assessment

 

Table of Contents 

1. Severe Hypertriglyceridemia Market Report Introduction

2. Executive Summary for Severe Hypertriglyceridemia

3. SWOT analysis of Severe Hypertriglyceridemia

4. Severe Hypertriglyceridemia Patient Share (%) Overview at a Glance

5. Severe Hypertriglyceridemia Market Overview at a Glance

6. Severe Hypertriglyceridemia Disease Background and Overview

7. Severe Hypertriglyceridemia Epidemiology and Patient Population

8. Country-Specific Patient Population of Severe Hypertriglyceridemia 

9. Severe Hypertriglyceridemia Current Treatment and Medical Practices

10. Severe Hypertriglyceridemia Unmet Needs

11. Severe Hypertriglyceridemia Emerging Therapies

12. Severe Hypertriglyceridemia Market Outlook

13. Country-Wise Severe Hypertriglyceridemia Market Analysis (2019–2032)

14. Severe Hypertriglyceridemia Market Access and Reimbursement of Therapies

15. Severe Hypertriglyceridemia Market Drivers

16. Severe Hypertriglyceridemia Market Barriers

17.  Severe Hypertriglyceridemia Appendix

18. Severe Hypertriglyceridemia Report Methodology

19. DelveInsight Capabilities

20. Disclaimer

21. About DelveInsight

 

About DelveInsight 

DelveInsight is a leading Healthcare Business Consultant, and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance.

It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight
Contact Person: Gaurav Bora
Email: Send Email
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Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
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Website: https://www.delveinsight.com/

 

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Oncolytic Virus Cancer Therapy Pipeline Assessment: FDA, EMA, and PMDA Approvals, Emerging Drugs, Clinical Trials, Therapeutic Analysis, and Growth Prospects | CG Oncology, Targovax, Transgene

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Oncolytic Virus Cancer Therapy pipeline constitutes 120+ key companies continuously working towards developing 125+ Oncolytic Virus Cancer Therapy treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Oncolytic Virus Cancer Therapy Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

Oncolytic Virus Cancer Therapy Pipeline Insight, 2024 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Oncolytic Virus Cancer Therapy Market.

 

Some of the key takeaways from the Oncolytic Virus Cancer Therapy Pipeline Report:

  • Companies across the globe are diligently working toward developing novel Oncolytic Virus Cancer Therapy treatment therapies with a considerable amount of success over the years. 
  • Oncolytic Virus Cancer Therapy companies working in the treatment market are DNAtrix, Nouscom, Astellas Pharma, CG Oncology, Targovax, Transgene, Istari Oncology, Targovax, Oncolytics Biotech, and others, are developing therapies for the Oncolytic Virus Cancer Therapy treatment 
  • Emerging Oncolytic Virus Cancer Therapy therapies in the different phases of clinical trials are- DNX 2440, NOUS PEV, ASP 9801, CG0070, ONCOS-102, TG 6002, PVS-RIPO, DNX-2401, ONCOS 102, Pelareorep, CG0070, and others are expected to have a significant impact on the Oncolytic Virus Cancer Therapy market in the coming years. 
  • In November 2022, The anti-PD-1 drug KEYTRUDA® (pembrolizumab) and CG0070 were combined in CG Oncology’s worldwide Phase 2 study (CORE1) for the treatment of patients with nonmuscle invasive bladder cancer (NMIBC) who were resistant to Bacillus Calmette-Guérin (BCG
  • In January 2022, Affibody AB (“Affibody”) and Lokon Pharma AB established a partnership to combine oncolytic viruses with Affibody® compounds.
  • In April 2022, New preclinical results will be presented at the American Association for Cancer Research (AACR) Annual Meeting 2022 (April 8–13), according to an announcement from OncoMyx Therapeutics. The information given at AACR 2022 shows that OncoMyx’s myxoma virus, which is multi-armed with IL-12 and decorin, infects and kills human multiple myeloma cells in vitro and exhibits dose-responsive effectiveness after intravenous (IV) injection in a mouse model of multiple myeloma.
  • In March 2022, An investigation into the therapeutic potential of intravenous VCN-01 oncolytic adenovirus in combination with or without standard-of-care (SoC) chemotherapy (gemcitabine/nab-paclitaxel) in patients with advanced solid tumours was published in a peer-reviewed journal, according to Synthetic Biologics, Inc. According to the studies, which were published in the Journal for ImmunoTherapy of Cancer, using VCN-01 as a treatment is doable, has a good safety profile, and has positive biological and clinical activity.These results help to frame the dose-finding process and guide the clinical development plan for VCN-01.
  • In March 2022, The initial dosage of the ground-breaking intravenous oncolytic viral product MVR-T3011 IV by ImmVira was completed in a Phase I clinical trial in China.
  • In December 2021, AstraZeneca exercised its first licence option for an Invir.IOTM oncolytic virus (OV) created as a result of their ongoing OV collaboration, Transgene reported. Transgene received a $8 million payment from AstraZeneca as a result of the exercise of this option for an OV, which involved integrating an unidentified transgene.

 

Oncolytic Virus Cancer Therapy Overview

Oncolytic virus (OV) cancer therapies are virus-based treatment modalities that infect and kill cancer cells, and by releasing tumor-specific antigens, also serve as an in situ cancer vaccine. Myxoma virus and reovirus are two examples of viruses that naturally target tumour cells while being nonpathogenic to healthy human cells.

 

Get a Free Sample PDF Report to know more about Oncolytic Virus Cancer Therapy Pipeline Therapeutic Assessment-

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Emerging Oncolytic Virus Cancer Therapy Drugs Under Different Phases of Clinical Development Include:

  • DNX 2440: DNAtrix
  • NOUS PEV: Nouscom
  • ASP 9801: Astellas Pharma
  • CG0070: CG Oncology
  • ONCOS-102: Targovax
  • TG 6002 : Transgene
  • PVS-RIPO: Istari Oncology
  • DNX-2401: DNAtrix
  • ONCOS 102: Targovax
  • Pelareorep: Oncolytics Biotech
  • CG0070: CG Oncolgy

 

Oncolytic Virus Cancer Therapy Route of Administration

Oncolytic Virus Cancer Therapy pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs, such as 

  • Intranasal
  • Intravenous
  • Oral
  • Oral/Intravenous
  • Parenteral
  • Subcutaneous
  • Subcutaneous/Intramuscular

 

Oncolytic Virus Cancer Therapy Molecule Type

Oncolytic Virus Cancer Therapy Products have been categorized under various Molecule types, such as

  • Oncolytic Viruse

 

Oncolytic Virus Cancer Therapy Pipeline Therapeutics Assessment

  • Oncolytic Virus Cancer Therapy Assessment by Product Type
  • Oncolytic Virus Cancer Therapy By Stage and Product Type
  • Oncolytic Virus Cancer Therapy Assessment by Route of Administration
  • Oncolytic Virus Cancer Therapy By Stage and Route of Administration
  • Oncolytic Virus Cancer Therapy Assessment by Molecule Type
  • Oncolytic Virus Cancer Therapy by Stage and Molecule Type

 

DelveInsight’s Oncolytic Virus Cancer Therapy Report covers around 125+ products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further Oncolytic Virus Cancer Therapy product details are provided in the report. Download the Oncolytic Virus Cancer Therapy pipeline report to learn more about the emerging Oncolytic Virus Cancer Therapy therapies

 

Some of the key companies in the Oncolytic Virus Cancer Therapy Therapeutics Market include:

Key companies developing therapies for Oncolytic Virus Cancer Therapy are –  Lokon Pharma, Merck, Wuhan Binhui Biotechnology, CG Oncology, Oncolys Biopharma, Replimune, Transgene, Sorrento Therapeutics, ORCA Therapeutics, TILT Biotherapeutics, BioEclipse Therapeutics, Oncolytics Biotech, Oncorus, DNAtrix, OncoMyx Therapeutics, Vyriad, Boehringer Ingelheim, IconOVir Bio, Imugene, Turnstone Biologics, Immvira Pharma, SillaJen Biotherapeutics, Advantagene, Nouscom, TOT Biopharm, Elicera Therapeutics, Takeda, Candel Therapeutics, Valo Therapeutics, Tessa Therapeutics, PsiOxus Therapeutics, KaliVir Immunotherapeutics, Oncos Therapeutics, Mustang Bio, Takara Bio, Vaxiion Therapeutics, Synthetic Biologics, Calidi Biotherapeutics, Genelux Corporation, Shanghai Sunway Biotech, BioInvent International AB, Guizhou Sinorda Biomedicine, EpicentRx, Hookipa Pharma Inc., Imvaq Therapeutics, Seneca Therapeutics, AmunBio, Orgenesis, Protheragen, Astellas Pharma, and others.

 

Oncolytic Virus Cancer Therapy Pipeline Analysis:

The Oncolytic Virus Cancer Therapy pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Oncolytic Virus Cancer Therapy with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Oncolytic Virus Cancer Therapy Treatment.
  • Oncolytic Virus Cancer Therapy key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Oncolytic Virus Cancer Therapy Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Oncolytic Virus Cancer Therapy market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about Oncolytic Virus Cancer Therapy drugs and therapies

 

Oncolytic Virus Cancer Therapy Pipeline Market Drivers

Increase in the number of patients with cancers, rising need for advanced and effective cancer therapeutics for improved quality of life are some of the important factors that are fueling the Oncolytic Virus Cancer Therapy Market.

 

Oncolytic Virus Cancer Therapy Pipeline Market Barriers 

However, lack of development, scaleup and commercialisation resources available to developers, lack of awareness about the new class of anticancer immunotherapy and other factors are creating obstacles in the Oncolytic Virus Cancer Therapy Market growth.

 

Scope of Oncolytic Virus Cancer Therapy Pipeline Drug Insight    

  • Coverage: Global
  • Key Oncolytic Virus Cancer Therapy Companies: DNAtrix, Nouscom, Astellas Pharma, CG Oncology, Targovax, Transgene, Istari Oncology, Targovax, Oncolytics Biotech, and others
  • Key Oncolytic Virus Cancer Therapy Therapies: DNX 2440, NOUS PEV, ASP 9801, CG0070, ONCOS-102, TG 6002, PVS-RIPO, DNX-2401, ONCOS 102, Pelareorep, CG0070, and others
  • Oncolytic Virus Cancer Therapy Therapeutic Assessment: Oncolytic Virus Cancer Therapy current marketed and Oncolytic Virus Cancer Therapy emerging therapies
  • Oncolytic Virus Cancer Therapy Market Dynamics: Oncolytic Virus Cancer Therapy market drivers and Oncolytic Virus Cancer Therapy market barriers 

 

Request for Sample PDF Report for Oncolytic Virus Cancer Therapy Pipeline Assessment and clinical trials

 

Table of Contents 

1. Oncolytic Virus Cancer Therapy Report Introduction

2. Oncolytic Virus Cancer Therapy Executive Summary

3. Oncolytic Virus Cancer Therapy Overview

4. Oncolytic Virus Cancer Therapy- Analytical Perspective In-depth Commercial Assessment

5. Oncolytic Virus Cancer Therapy Pipeline Therapeutics

6. Oncolytic Virus Cancer Therapy Late Stage Products (Phase II/III)

7. Oncolytic Virus Cancer Therapy Mid Stage Products (Phase II)

8. Oncolytic Virus Cancer Therapy Early Stage Products (Phase I)

9. Oncolytic Virus Cancer Therapy Preclinical Stage Products

10. Oncolytic Virus Cancer Therapy Therapeutics Assessment

11. Oncolytic Virus Cancer Therapy Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. Oncolytic Virus Cancer Therapy Key Companies

14. Oncolytic Virus Cancer Therapy Key Products

15. Oncolytic Virus Cancer Therapy Unmet Needs

16 . Oncolytic Virus Cancer Therapy Market Drivers and Barriers

17. Oncolytic Virus Cancer Therapy Future Perspectives and Conclusion

18. Oncolytic Virus Cancer Therapy Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight

 

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight
Contact Person: Gaurav Bora
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/

 

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Hepatic Cirrhosis Market to Exhibit Rapid Growth Rate During the Forecast Period (2023-2032), Investigates DelveInsight | Mallinckrodt, Galectin Therapeutics, Norgine, Otsuka Beijing Research

“Hepatic Cirrhosis Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Hepatic Cirrhosis, historical and forecasted epidemiology as well as the Hepatic Cirrhosis market trends in the 7MM.

DelveInsight’s “Hepatic Cirrhosis Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Hepatic Cirrhosis, historical and forecasted epidemiology as well as the Hepatic Cirrhosis market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.

 

To Know in detail about the Hepatic Cirrhosis market outlook, drug uptake, treatment scenario and epidemiology trends, Click here; Hepatic Cirrhosis Market Forecast

 

Some of the key facts of the Hepatic Cirrhosis Market Report: 

  • The Hepatic Cirrhosis market size is anticipated to grow with a significant CAGR during the study period (2019-2032)
  • The global occurrence of cirrhosis remains uncertain, with estimates suggesting a prevalence ranging from 0.15% to 0.27% in the United States, according to Sharma and John’s findings in 2021.
  • The strategies employed in drug discovery and development for liver fibrosis and cirrhosis are advancing, utilizing increasingly sophisticated methods. This involves harnessing extensive human ‘big data’ resources and integrating high-throughput techniques to explore new drugs or combinations. Examples include the use of innovative technologies such as liver-on-a-chip devices and hepatic organoids/spheres.
  • Key Hepatic Cirrhosis Companies: Mallinckrodt, Galectin Therapeutics, Norgine, Otsuka Beijing Research, Conatus Pharmaceuticals Inc., Bristol-Myers Squibb, Grifols Biologicals, LLC, Horizon Pharma, Vedanta Biosciences, Inc., Bausch Health, and others
  • Key Hepatic Cirrhosis Therapies: Terlipressin, Belapectin, NRL972, MNK6106, Tolvaptan, IDN-6556, BMS-986263, Albumin Infusion, HPN-100, VE303, Rifaximin, and others
  • The Hepatic Cirrhosis epidemiology based on gender analyzed that males are more affected with Hepatic Cirrhosis than females.
  • The Hepatic Cirrhosis market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Hepatic Cirrhosis pipeline products will significantly revolutionize the Hepatic Cirrhosis market dynamics.

 

Hepatic Cirrhosis Overview

Hepatic cirrhosis, often simply referred to as cirrhosis, is a late stage of scarring (fibrosis) of the liver caused by many forms of liver diseases and conditions, such as hepatitis and chronic alcoholism. Each time your liver is injured, it tries to repair itself. In the process, scar tissue forms. As the cirrhosis progresses, more and more scar tissue forms, making it difficult for the liver to function.

 

Get a Free sample for the Hepatic Cirrhosis Market Forecast, Size & Share Analysis Report: 

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Hepatic Cirrhosis Epidemiology

The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2019 to 2032. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.

 

Hepatic Cirrhosis Epidemiology Segmentation:

The Hepatic Cirrhosis market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into:

  • Total Prevalence of Hepatic Cirrhosis
  • Prevalent Cases of Hepatic Cirrhosis by severity
  • Gender-specific Prevalence of Hepatic Cirrhosis
  • Diagnosed Cases of Episodic and Chronic Hepatic Cirrhosis

 

Download the report to understand which factors are driving Hepatic Cirrhosis epidemiology trends @ Hepatic Cirrhosis Epidemiology Forecast

 

Hepatic Cirrhosis Drugs Uptake and Pipeline Development Activities

The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Hepatic Cirrhosis market or expected to get launched during the study period. The analysis covers Hepatic Cirrhosis market uptake by drugs, patient uptake by therapies, and sales of each drug. 

Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.

The report also covers the Hepatic Cirrhosis Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.

 

Hepatic Cirrhosis Therapies and Key Companies

  • Terlipressin: Mallinckrodt
  • Belapectin: Galectin Therapeutics
  • NRL972: Norgine
  • MNK6106: Mallinckrodt
  • Tolvaptan: Otsuka Beijing Research
  • IDN-6556: Conatus Pharmaceuticals Inc.
  • BMS-986263: Bristol-Myers Squibb
  • Albumin Infusion: Grifols Biologicals, LLC
  • HPN-100: Horizon Pharma
  • VE303: Vedanta Biosciences, Inc.
  • Rifaximin: Bausch Health

 

Discover more about therapies set to grab major Hepatic Cirrhosis market share @ Hepatic Cirrhosis Treatment Landscape

 

Scope of the Hepatic Cirrhosis Market Report

  • Study Period: 2019–2032
  • Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
  • Key Hepatic Cirrhosis Companies: Mallinckrodt, Galectin Therapeutics, Norgine, Otsuka Beijing Research, Conatus Pharmaceuticals Inc., Bristol-Myers Squibb, Grifols Biologicals, LLC, Horizon Pharma, Vedanta Biosciences, Inc., Bausch Health, and others
  • Key Hepatic Cirrhosis Therapies: Terlipressin, Belapectin, NRL972, MNK6106, Tolvaptan, IDN-6556, BMS-986263, Albumin Infusion, HPN-100, VE303, Rifaximin, and others
  • Hepatic Cirrhosis Therapeutic Assessment: Hepatic Cirrhosis current marketed and Hepatic Cirrhosis emerging therapies
  • Hepatic Cirrhosis Market Dynamics: Hepatic Cirrhosis market drivers and Hepatic Cirrhosis market barriers 
  • Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Hepatic Cirrhosis Unmet Needs, KOL’s views, Analyst’s views, Hepatic Cirrhosis Market Access and Reimbursement 

 

To know more about Hepatic Cirrhosis companies working in the treatment market, visit @ Hepatic Cirrhosis Clinical Trials and Therapeutic Assessment

 

Table of Contents 

1. Hepatic Cirrhosis Market Report Introduction

2. Executive Summary for Hepatic Cirrhosis

3. SWOT analysis of Hepatic Cirrhosis

4. Hepatic Cirrhosis Patient Share (%) Overview at a Glance

5. Hepatic Cirrhosis Market Overview at a Glance

6. Hepatic Cirrhosis Disease Background and Overview

7. Hepatic Cirrhosis Epidemiology and Patient Population

8. Country-Specific Patient Population of Hepatic Cirrhosis 

9. Hepatic Cirrhosis Current Treatment and Medical Practices

10. Hepatic Cirrhosis Unmet Needs

11. Hepatic Cirrhosis Emerging Therapies

12. Hepatic Cirrhosis Market Outlook

13. Country-Wise Hepatic Cirrhosis Market Analysis (2019–2032)

14. Hepatic Cirrhosis Market Access and Reimbursement of Therapies

15. Hepatic Cirrhosis Market Drivers

16. Hepatic Cirrhosis Market Barriers

17.  Hepatic Cirrhosis Appendix

18. Hepatic Cirrhosis Report Methodology

19. DelveInsight Capabilities

20. Disclaimer

21. About DelveInsight

 

About DelveInsight 

DelveInsight is a leading Healthcare Business Consultant, and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance.

It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight
Contact Person: Gaurav Bora
Email: Send Email
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Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/

 

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To view the original version on ABNewswire visit: Hepatic Cirrhosis Market to Exhibit Rapid Growth Rate During the Forecast Period (2023-2032), Investigates DelveInsight | Mallinckrodt, Galectin Therapeutics, Norgine, Otsuka Beijing Research

Celiac Disease Market to Observe Impressive Growth During the Forecast Period (2023-2032), Evaluates DelveInsight | Zedira, Dr. Falk Pharma, Takeda, ImmunoGenX, Provention Bio, Sanofi, Topas

“Celiac Disease Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Celiac Disease, historical and forecasted epidemiology as well as the Celiac Disease market trends in the 7MM.

DelveInsight’s “Celiac Disease Market Insights, Epidemiology, and Market Forecast-2032″ report offers an in-depth understanding of the Celiac Disease, historical and forecasted epidemiology as well as the Celiac Disease market trends in the United States, EU4 (Germany, Spain, Italy, France) the United Kingdom and Japan.

 

To Know in detail about the Celiac Disease market outlook, drug uptake, treatment scenario and epidemiology trends, Click here; Celiac Disease Market Forecast

 

Some of the key facts of the Celiac Disease Market Report: 

  • The Celiac Disease market size is anticipated to grow with a significant CAGR during the study period (2019-2032)
  • In July 2022, Due to dismal interim findings, 9 Metres Biopharma terminated their Phase III product larazotide for the treatment of celiac disease.
  • In October 2022, Takeda and Zedira and Dr. Falk Pharma reached an agreement to develop ZED1227/TAK-227 for the treatment of celiac disease
  • The Celiac Disease Foundation states that celiac disease is a dangerous autoimmune condition that affects one in every 100 persons globally. Additionally, 2.5 million Americans are untreated and at danger of developing long-term health issues
  • In 2021, there were 1.4 million cases of Celiac Disease that had been diagnosed as being prevalent worldwide, with 0.7 million of those cases occurring in the United States
  • Key Celiac Disease Companies: Zedira, Dr. Falk Pharma, Takeda, ImmunoGenX, Provention Bio, Sanofi, Topas Therapeutics GmbH, Pfizer, 9 Meters Biopharma, Inc., ChemoCentryx, BioLineRx, Ltd., and others
  • Key Celiac Disease Therapies: TAK-227/ZED1227, Latiglutenase(IMGX003), Ordesekimab, TAK-101 and Zamaglutenase, TPM502, Ritlecitinib, TAK-062, larazotide acetate, CCX282-B, BL-7010, and others
  • The Celiac Disease epidemiology based on gender analyzed that, females are affected more than males
  • The Celiac Disease market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Celiac Disease pipeline products will significantly revolutionize the Celiac Disease market dynamics.

 

Celiac Disease Overview

In contrast to other autoimmune diseases, celiac disease exhibits unusual characteristics, such as the complete repair of mucosal injury as well as the reversibility of its progression and chronic dynamics, with complete avoidance of gluten.

 

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Celiac Disease Epidemiology

The epidemiology section provides insights into the historical, current, and forecasted epidemiology trends in the seven major countries (7MM) from 2019 to 2032. It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides a detailed analysis of the diagnosed patient pool and future trends.

 

Celiac Disease Epidemiology Segmentation:

The Celiac Disease market report proffers epidemiological analysis for the study period 2019–2032 in the 7MM segmented into:

  • Total Prevalence of Celiac Disease
  • Prevalent Cases of Celiac Disease by severity
  • Gender-specific Prevalence of Celiac Disease
  • Diagnosed Cases of Episodic and Chronic Celiac Disease

 

Download the report to understand which factors are driving Celiac Disease epidemiology trends @ Celiac Disease Epidemiology Forecast

 

Celiac Disease Drugs Uptake and Pipeline Development Activities

The drugs uptake section focuses on the rate of uptake of the potential drugs recently launched in the Celiac Disease market or expected to get launched during the study period. The analysis covers Celiac Disease market uptake by drugs, patient uptake by therapies, and sales of each drug. 

Moreover, the therapeutics assessment section helps understand the drugs with the most rapid uptake and the reasons behind the maximal use of the drugs. Additionally, it compares the drugs based on market share.

The report also covers the Celiac Disease Pipeline Development Activities. It provides valuable insights about different therapeutic candidates in various stages and the key companies involved in developing targeted therapeutics. It also analyzes recent developments such as collaborations, acquisitions, mergers, licensing patent details, and other information for emerging therapies.

 

Celiac Disease Therapies and Key Companies

  • TAK-227/ZED1227: Zedira, Dr. Falk Pharma, and Takeda
  • Latiglutenase(IMGX003): ImmunoGenX
  • Ordesekimab: Provention Bio/Sanofi
  • TAK-101 and Zamaglutenase: Takeda
  • TPM502: Topas Therapeutics GmbH
  • Ritlecitinib: Pfizer
  • TAK-062: Takeda
  • larazotide acetate: 9 Meters Biopharma, Inc.
  • CCX282-B: ChemoCentryx
  • BL-7010: BioLineRx, Ltd.

 

Discover more about therapies set to grab major Celiac Disease market share @ Celiac Disease Treatment Market

 

Celiac Disease Market Strengths

  • The pipeline activity of Celiac Disease is quite efficient with the presence of variable key players such as ImmunogenX, Provention Bio, Takeda, etc., which are efficiently involved in developing milestone treatment options.

 

Celiac Disease Market Opportunities

  • Several organizations such as Celiac Disease Foundation, National Celiac Association (NCA), American Celiac Disease Alliance (Celiac Disease A), Coelic UKetc. are actively working to provide information and awareness of the disorder

 

Scope of the Celiac Disease Market Report

  • Study Period: 2019–2032
  • Coverage: 7MM [The United States, EU5 (Germany, France, Italy, Spain, and the United Kingdom), and Japan]
  • Key Celiac Disease Companies: Zedira, Dr. Falk Pharma, Takeda, ImmunoGenX, Provention Bio, Sanofi, Topas Therapeutics GmbH, Pfizer, 9 Meters Biopharma, Inc., ChemoCentryx, BioLineRx, Ltd., and others
  • Key Celiac Disease Therapies: TAK-227/ZED1227, Latiglutenase(IMGX003), Ordesekimab, TAK-101 and Zamaglutenase, TPM502, Ritlecitinib, TAK-062, larazotide acetate, CCX282-B, BL-7010, and others
  • Celiac Disease Therapeutic Assessment: Celiac Disease current marketed and Celiac Disease emerging therapies
  • Celiac Disease Market Dynamics: Celiac Disease market drivers and Celiac Disease market barriers 
  • Competitive Intelligence Analysis: SWOT analysis, PESTLE analysis, Porter’s five forces, BCG Matrix, Market entry strategies
  • Celiac Disease Unmet Needs, KOL’s views, Analyst’s views, Celiac Disease Market Access and Reimbursement 

 

To know more about Celiac Disease companies working in the treatment market, visit @ Celiac Disease Clinical Trials and Therapeutic Assessment

 

Table of Contents 

1. Celiac Disease Market Report Introduction

2. Executive Summary for Celiac Disease

3. SWOT analysis of Celiac Disease

4. Celiac Disease Patient Share (%) Overview at a Glance

5. Celiac Disease Market Overview at a Glance

6. Celiac Disease Disease Background and Overview

7. Celiac Disease Epidemiology and Patient Population

8. Country-Specific Patient Population of Celiac Disease 

9. Celiac Disease Current Treatment and Medical Practices

10. Celiac Disease Unmet Needs

11. Celiac Disease Emerging Therapies

12. Celiac Disease Market Outlook

13. Country-Wise Celiac Disease Market Analysis (2019–2032)

14. Celiac Disease Market Access and Reimbursement of Therapies

15. Celiac Disease Market Drivers

16. Celiac Disease Market Barriers

17.  Celiac Disease Appendix

18. Celiac Disease Report Methodology

19. DelveInsight Capabilities

20. Disclaimer

21. About DelveInsight

 

About DelveInsight 

DelveInsight is a leading Healthcare Business Consultant, and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance.

It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate the business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight
Contact Person: Gaurav Bora
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/

 

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To view the original version on ABNewswire visit: Celiac Disease Market to Observe Impressive Growth During the Forecast Period (2023-2032), Evaluates DelveInsight | Zedira, Dr. Falk Pharma, Takeda, ImmunoGenX, Provention Bio, Sanofi, Topas

Advanced Ovarian Cancer Pipeline Analysis, 2024 Updates | Latest FDA, EMA, and PMDA Approvals | Pfizer, Daiichi Sankyo, Astellas Pharma, Jiangsu HengRui, Boehringer Ingelheim, Impact Therapeutics

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Advanced Ovarian Cancer pipeline constitutes 50+ key companies continuously working towards developing 50+ Advanced Ovarian Cancer treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

The Advanced Ovarian Cancer Pipeline report embraces in-depth commercial and clinical assessment of the pipeline products from the pre-clinical developmental phase to the marketed phase. The report also covers a detailed description of the drug, including the mechanism of action of the drug, clinical studies, NDA approvals (if any), and product development activities comprising the technology, collaborations, mergers acquisition, funding, designations, and other product-related details.

 

Advanced Ovarian Cancer Pipeline Insight, 2024 report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Advanced Ovarian Cancer Market.

 

Some of the key takeaways from the Advanced Ovarian Cancer Pipeline Report:

  • Companies across the globe are diligently working toward developing novel Advanced Ovarian Cancer treatment therapies with a considerable amount of success over the years. 
  • Advanced Ovarian Cancer companies working in the treatment market are Daiichi Sankyo, Inc, Amgen, Compugen Ltd, NextCure, Sonnet BioTherapeutics, SOTIO Biotech B.V., Akeso, Allarity Therapeutics, Merck Sharp & Dohme, CanariaBio Inc., Allarity Therapeutics, CSPC ZhongQi Pharmaceutical Technology Co., Ltd., and others, are developing therapies for the Advanced Ovarian Cancer treatment 
  • Emerging Advanced Ovarian Cancer therapies in the different phases of clinical trials are- DS-6000a, AMG-794, COM701, NC762, SON-1010, SOT101, AK112, 2X-121, Pembrolizumab, Oregovomab, Stenoparib, DP-303c, and others are expected to have a significant impact on the Advanced Ovarian Cancer market in the coming years.   
  • In December 2023, Allarity Therapeutics, Inc. (“Allarity” or the “Company”), a pharmaceutical enterprise in the clinical stage developing innovative oncology treatments alongside drug-specific DRP® companion diagnostics for personalized cancer care, has disclosed promising initial findings from its ongoing Phase 2 clinical trial. This trial assesses the effectiveness of its PARP inhibitor, stenoparib, in treating women diagnosed with advanced ovarian cancer (AOC). Among the initial data analysis involving five assessable patients, one patient achieved a complete response, while the remaining four exhibited stable disease.
  • In July 2022, CanariaBio Inc. is conducting a Phase II single-arm open-label study to assess the combined use of oregovomab and niraparib as an immune priming strategy in individuals diagnosed with platinum-sensitive recurrent ovarian cancer. The study aims to screen around 15 subjects to enroll approximately 10 participants for evaluation. Its primary objective is to evaluate the safety and efficacy of the oregovomab and niraparib combination as an immune priming approach in patients facing platinum-sensitive recurrent ovarian cancer.
  • In June 2022, CanariaBio Inc. declared that it has achieved 50% of the intended enrollment goal of 602 patients for its pivotal Phase III clinical trial involving its primary product, oregovomab. This trial investigates the use of oregovomab in combination with standard chemotherapy (carboplatin and paclitaxel) for treating frontline advanced ovarian cancer patients.

 

Advanced Ovarian Cancer Overview

When it comes to women with gynecological cancer diagnoses, ovarian cancer is the most common cause of death. In general, it ranks as the fifth most common cause of mortality for women. Poor outcomes from this disease are caused by the majority of cases being discovered at an advanced stage.

 

Get a Free Sample PDF Report to know more about Advanced Ovarian Cancer Pipeline Therapeutic Assessment-

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Emerging Advanced Ovarian Cancer Drugs Under Different Phases of Clinical Development Include:

  • DS-6000a: Daiichi Sankyo, Inc
  • AMG-794: Amgen
  • COM701: Compugen Ltd
  • NC762: NextCure
  • SON-1010: Sonnet BioTherapeutics
  • SOT101: SOTIO Biotech B.V.
  • AK112: Akeso
  • 2X-121: Allarity Therapeutics
  • Pembrolizumab: Merck Sharp & Dohme
  • Oregovomab: CanariaBio Inc.
  • Stenoparib: Allarity Therapeutics
  • DP-303c: CSPC ZhongQi Pharmaceutical Technology Co., Ltd.

 

Advanced Ovarian Cancer Route of Administration

Advanced Ovarian Cancer pipeline report provides the therapeutic assessment of the pipeline drugs by the Route of Administration. Products have been categorized under various ROAs, such as 

  • Oral
  • Parenteral
  • Intravenous
  • Subcutaneous
  • Topical.

 

Advanced Ovarian Cancer Molecule Type

Advanced Ovarian Cancer Products have been categorized under various Molecule types, such as

  • Monoclonal Antibody
  • Peptides
  • Polymer
  • Small molecule
  • Gene therapy

 

Advanced Ovarian Cancer Pipeline Therapeutics Assessment

  • Advanced Ovarian Cancer Assessment by Product Type
  • Advanced Ovarian Cancer By Stage and Product Type
  • Advanced Ovarian Cancer Assessment by Route of Administration
  • Advanced Ovarian Cancer By Stage and Route of Administration
  • Advanced Ovarian Cancer Assessment by Molecule Type
  • Advanced Ovarian Cancer by Stage and Molecule Type

 

DelveInsight’s Advanced Ovarian Cancer Report covers around 50+ products under different phases of clinical development like

  • Late-stage products (Phase III)
  • Mid-stage products (Phase II)
  • Early-stage product (Phase I)
  • Pre-clinical and Discovery stage candidates
  • Discontinued & Inactive candidates
  • Route of Administration

 

Further Advanced Ovarian Cancer product details are provided in the report. Download the Advanced Ovarian Cancer pipeline report to learn more about the emerging Advanced Ovarian Cancer therapies

 

Some of the key companies in the Advanced Ovarian Cancer Therapeutics Market include:

Key companies developing therapies for Advanced Ovarian Cancer are – Pfizer, Daiichi Sankyo, Inc., Astellas Pharma Inc, Jiangsu HengRui Medicine Co., Ltd., Boehringer Ingelheim, Impact Therapeutics, Inc., Glycotope, ImmunoGen, OncoQuest, Lee’s Pharmaceutical, Allarity Therapeutics, AstraZeneca, Jiangxi Qingfeng Pharmaceutical Co. Ltd., Bayer, Xennials Therapeutics, CSPC ZhongQi Pharmaceutical Technology Co., Ltd., Ellipses Pharma, Merck KGaA, Puma Biotechnology, Inc., MaxCyte, Inc., Chia Tai Tianqing Pharmaceutical Group Co., Ltd., and others.

 

Advanced Ovarian Cancer Pipeline Analysis:

The Advanced Ovarian Cancer pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Advanced Ovarian Cancer with aggregate therapies developed by each company for the same.
  • It accesses the Different therapeutic candidates segmented into early-stage, mid-stage, and late-stage of development for Advanced Ovarian Cancer Treatment.
  • Advanced Ovarian Cancer key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Advanced Ovarian Cancer Drugs under development based on the stage of development, route of administration, target receptor, monotherapy or combination therapy, a different mechanism of action, and molecular type. 
  • Detailed analysis of collaborations (company-company collaborations and company-academia collaborations), licensing agreement and financing details for future advancement of the Advanced Ovarian Cancer market.

The report is built using data and information traced from the researcher’s proprietary databases, company/university websites, clinical trial registries, conferences, SEC filings, investor presentations, and featured press releases from company/university websites and industry-specific third-party sources, etc.

 

Download Sample PDF Report to know more about Advanced Ovarian Cancer drugs and therapies

 

Advanced Ovarian Cancer Pipeline Market Drivers

  • Increasing prevalence of Advanced Ovarian Cancer, increasing research and development activities, launch of novel drugs are some of the important factors that are fueling the Advanced Ovarian Cancer Market.

 

Advanced Ovarian Cancer Pipeline Market Barriers

  • However, huge expenditure of the treatment methods, adverse effects associated with the drugs and other factors are creating obstacles in the Advanced Ovarian Cancer Market growth.

 

Scope of Advanced Ovarian Cancer Pipeline Drug Insight    

  • Coverage: Global
  • Key Advanced Ovarian Cancer Companies: Daiichi Sankyo, Inc, Amgen, Compugen Ltd, NextCure, Sonnet BioTherapeutics, SOTIO Biotech B.V., Akeso, Allarity Therapeutics, Merck Sharp & Dohme, CanariaBio Inc., Allarity Therapeutics, CSPC ZhongQi Pharmaceutical Technology Co., Ltd., and others
  • Key Advanced Ovarian Cancer Therapies: DS-6000a, AMG-794, COM701, NC762, SON-1010, SOT101, AK112, 2X-121, Pembrolizumab, Oregovomab, Stenoparib, DP-303c, and others
  • Advanced Ovarian Cancer Therapeutic Assessment: Advanced Ovarian Cancer current marketed and Advanced Ovarian Cancer emerging therapies
  • Advanced Ovarian Cancer Market Dynamics: Advanced Ovarian Cancer market drivers and Advanced Ovarian Cancer market barriers 

 

Request for Sample PDF Report for Advanced Ovarian Cancer Pipeline Assessment and clinical trials

 

Table of Contents

1. Advanced Ovarian Cancer Report Introduction

2. Advanced Ovarian Cancer Executive Summary

3. Advanced Ovarian Cancer Overview

4. Advanced Ovarian Cancer- Analytical Perspective In-depth Commercial Assessment

5. Advanced Ovarian Cancer Pipeline Therapeutics

6. Advanced Ovarian Cancer Late Stage Products (Phase II/III)

7. Advanced Ovarian Cancer Mid Stage Products (Phase II)

8. Advanced Ovarian Cancer Early Stage Products (Phase I)

9. Advanced Ovarian Cancer Preclinical Stage Products

10. Advanced Ovarian Cancer Therapeutics Assessment

11. Advanced Ovarian Cancer Inactive Products

12. Company-University Collaborations (Licensing/Partnering) Analysis

13. Advanced Ovarian Cancer Key Companies

14. Advanced Ovarian Cancer Key Products

15. Advanced Ovarian Cancer Unmet Needs

16 . Advanced Ovarian Cancer Market Drivers and Barriers

17. Advanced Ovarian Cancer Future Perspectives and Conclusion

18. Advanced Ovarian Cancer Analyst Views

19. Appendix

20. About DelveInsight

 

About DelveInsight

 

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

Media Contact
Company Name: DelveInsight
Contact Person: Gaurav Bora
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432
City: Las Vegas
State: NV
Country: United States
Website: https://www.delveinsight.com/

 

Press Release Distributed by ABNewswire.com

To view the original version on ABNewswire visit: Advanced Ovarian Cancer Pipeline Analysis, 2024 Updates | Latest FDA, EMA, and PMDA Approvals | Pfizer, Daiichi Sankyo, Astellas Pharma, Jiangsu HengRui, Boehringer Ingelheim, Impact Therapeutics

HER2 negative Breast Cancer Pipeline Report (2024): Analysis of Clinical Trials, Therapies, Route of Administration, Mechanism of Action and Developments | DelveInsight

“HER2 negative Breast Cancer Pipeline”

HER2 negative Breast Cancer Pipeline involves 85+ key companies continuously working towards developing 85+ HER2 negative Breast Cancer treatment therapies, as per DelveInsight

 

DelveInsight’s HER2 negative Breast Cancer Pipeline Insight 2024 report offers exhaustive global coverage of available, marketed, and pipeline therapies in different phases of clinical development, major pharmaceutical companies working to advance the pipeline space, and future growth potential of the HER2 negative Breast Cancer pipeline domain.

 

Click here to know more about the HER2 negative Breast Cancer Pipeline report offerings: HER2 negative Breast Cancer Pipeline Analysis

 

Some of the essential takeaways from the HER2 negative Breast Cancer Pipeline report:

  • DelveInsight’s HER2 negative Breast Cancer Pipeline analysis depicts a robust space with 85+ active players working to develop 85+ pipeline treatment therapies.
  • Some of the key pharmaceutical companies working to develop potential drug candidates to improve the HER2 negative Breast Cancer treatment scenario include BeiGene, Olema Pharmaceuticals, AstraZeneca, Radius Health, Adagene Inc, H3 Biomedicine Inc., Daiichi Sankyo, Inc., Shanghai Hengrui Pharmaceutical Co., Ltd., OncoSec Medical Incorporated, CSPC ZhongQi Pharmaceutical Technology Co., Ltd., Pfizer, InventisBio Co., Ltd, Hoffmann-La Roche, Angiochem, Bristol-Myers Squibb, Eisai Co., Ltd., Context Therapeutics, Boehringer Ingelheim, CytomX Therapeutics, Beta Pharma (Suzhou) Co., Ltd., Eli Lilly and Company, Laekna Limited, Sermonix Pharmaceuticals Inc., Modra Pharmaceuticals, MedImmune LLC, QED Therapeutics, Inc., Tyme, Inc., PIQUR Therapeutics, Pfizer, Merus N.V., Seagen, Relay Therapeutics, Inc., Blueprint Medicines Corporation, TransThera Sciences (Nanjing), Inc., HUTCHMED, VelosBio Inc., Dantari, Inc., GlaxoSmithKline, G1 Therapeutics, Inc., Spectrum Pharmaceuticals, Inc, Taizhou EOC Pharma Co., Ltd., Xuanzhu Biopharmaceutical Co., Ltd., Regor Pharmaceuticals Inc, Astex Pharmaceuticals, Inc., Kind Pharmaceuticals LLC, Genor Biopharma Co., Ltd., Jiangsu Simcere Pharmaceutical Co., Ltd., Nerviano Medical Sciences, Tolmar Inc., Zeno Alpha Inc., Accutar Biotechnology Inc, Jiangsu Hansoh Pharmaceutical Co., Ltd., Zenith Epigenetics, Cantargia, BioLite, Inc., PharmAbcine, Ayala Pharmaceuticals, Inc., ERYtech Pharma, SynCore Biotechnology Co., Ltd., Phoenix Molecular Designs, Chipscreen Biosciences, Ltd., OncoTherapy Science, Inc., OncoPep, Inc., and many others.
  • Essential HER2 negative Breast Cancer pipeline therapies such as BGB-290, OP-1250, AZD9833, Elacestrant, ADG106, H3B-6545, Dato-DXd, HRS8807, TAVO, Mitoxantrone Hydrochloride, Gedatolisib, D-0502, Ipatasertib, ANG1005, Nivolumab, Ipilimumab, Lenvatinib, Onapristone, Xentuzumab, CX-2009, BPI-1178, LY3484356, Afuresertib, Lasofoxifene, ModraDoc006/r, MEDI4736, Infigratinib, SM-88, PQR309, PF-07248144, MCLA-128, SGN-CD228A, RLY-2608, BLU-222, TT-00420, HMPL-013, Zilovertamab vedotin, DAN-222, Niraparib, G1T38, Poziotinib Hydrochloride, EOC202, XZP-3287, RGT-419B, ASTX727, AND019, Lerociclib, SGN-STNV, SCR-6852, NMS-03305293, TOL2506, ZN-c5, AC682, HS-10342, ZEN003694, Nadunolimab, BLEX 404, Olinvacimab, AL101, eryaspase, EndoTAG-1, PMD-026, Chiauranib, OTS167PO, PVX-410, and others are under development in different phases of clinical trials.
  • In January 2022, Celcuity announced that the U.S. Food and Drug Administration (FDA) had granted Fast Track designation to the Company’s lead drug candidate, gedatolisib, for the treatment of patients with HR+/HER2- metastatic breast cancer after progression on CDK4/6 therapy.
  • In December 2021, H3 Biomedicine Inc. (H3), announced the presentation of two posters at the 2021 San Antonio Breast Cancer Symposium (SABCS) being held in a hybrid format on December 7- 10, 2021. The presentations include interim investigational data from H3’s ongoing clinical development program, H3B-6545, a potential first-in-class, orally available Selective ERα Covalent Antagonist (SERCA), in women with ER-positive, HER2-negative breast cancer.
  • The investigational oral selective estrogen receptor degrader (SERD) elacestrant significantly decreased the risk of death or disease progression and increased progression-free survival compared with standard-of-care endocrine therapy for postmenopausal patients with estrogen receptor (ER)-positive/HER2-negative metastatic breast cancers that progressed on prior endocrine and targeted therapies, according to results from the phase III EMERALD trial, which were presented at the San Antonio Breast Cancer Symposium, held December 7-10, 2021.
  • In November 2021, Olema Pharmaceuticals, Inc. announced the first clinical data from the Phase 1 dose-escalation portion of the ongoing Phase 1/2 clinical trial of OP-1250, a complete estrogen receptor (ER) antagonist (CERAN) and a selective ER degrader (SERD) in development for the treatment of metastatic breast cancer and other women’s cancers.

 

Request a sample and discover more about the HER2 negative Breast Cancer Emerging Therapies @ https://www.delveinsight.com/sample-request/her2-negative-breast-cancer-pipeline-insight

 

The HER2 negative Breast Cancer pipeline report lays down detailed profiles of the pipeline assets, comparative analysis of clinical and non-clinical stage HER2 negative Breast Cancer products, inactive and dormant assets, comprehensive assessment of driving and restraining factors, as well as the opportunities and risks in the HER2 negative Breast Cancer pipeline landscape.

 

HER2 negative Breast Cancer Overview

Most Breast Cancers express the Estrogen Receptor (ER) receptor and are negative for the human epidermal growth factor receptor 2 (HER2) receptor. ER+/ HER2 – ve Breast Cancer includes tumors that are ER-positive and PR positive, but negative for HER2. ER+/ HER2 – ve Breast Cancer is heterogeneous and accounts for about 70% of all breast cancers. HER2” stands for human epidermal growth factor receptor 2. There are various types of breast cancer, some have hormone receptors like estrogen or progesterone (some have both) and are called ER+ or PR+ breast cancer respectively.

 

Find out more about the disease and recent developments in HER2 negative Breast Cancer Pipeline landscape @ HER2 negative Breast Cancer Drugs in pipeline

 

HER2 negative Breast Cancer Therapeutics Assessment

The HER2 negative Breast Cancer Pipeline report proffers an integral view of the HER2 negative Breast Cancer emerging novel therapies segmented by Stage, Product Type, Molecule Type, Mechanism of Action, and Route of Administration.

 

Scope of the HER2 negative Breast Cancer Pipeline Report

  • Coverage: Global
  • Therapeutic Assessment By HER2 negative Breast Cancer Product Type: Mono, Combination, Mono/Combination
  • Therapeutic Assessment By HER2 negative Breast Cancer Clinical Stages: Discovery, Pre-clinical, Phase I, Phase II, Phase III, Pre-registration, Inactive candidates
  • Therapeutics Assessment By HER2 negative Breast Cancer Therapeutics Route of Administration: Oral, Intravenous, Inhalation, Subcutaneous
  • Therapeutics Assessment By HER2 negative Breast Cancer Therapies Molecule Type: Gene therapy, Stem cell therapy, Small molecules
  • Therapeutics Assessment By HER2 negative Breast Cancer Therapies Mechanism of Action: Selective estrogen receptor degrader, Estrogen receptor alpha antagonist, Phosphoinositide 3-kinase (PI3K) inhibitor, Selective estrogen receptor degraders
  • Key HER2 negative Breast Cancer Companies: BeiGene, Olema Pharmaceuticals, AstraZeneca, Radius Health, Adagene Inc, H3 Biomedicine Inc., Daiichi Sankyo, Inc., Shanghai Hengrui Pharmaceutical Co., Ltd., OncoSec Medical Incorporated, CSPC ZhongQi Pharmaceutical Technology Co., Ltd., Pfizer, InventisBio Co., Ltd, Hoffmann-La Roche, Angiochem, Bristol-Myers Squibb, Eisai Co., Ltd., Context Therapeutics, Boehringer Ingelheim, CytomX Therapeutics, Beta Pharma (Suzhou) Co., Ltd., Eli Lilly and Company, Laekna Limited, Sermonix Pharmaceuticals Inc., Modra Pharmaceuticals, MedImmune LLC, QED Therapeutics, Inc., Tyme, Inc., PIQUR Therapeutics, Pfizer, Merus N.V., Seagen, Relay Therapeutics, Inc., Blueprint Medicines Corporation, TransThera Sciences (Nanjing), Inc., HUTCHMED, VelosBio Inc., Dantari, Inc., GlaxoSmithKline, G1 Therapeutics, Inc., Spectrum Pharmaceuticals, Inc, Taizhou EOC Pharma Co., Ltd., Xuanzhu Biopharmaceutical Co., Ltd., Regor Pharmaceuticals Inc, Astex Pharmaceuticals, Inc., Kind Pharmaceuticals LLC, Genor Biopharma Co., Ltd., Jiangsu Simcere Pharmaceutical Co., Ltd., Nerviano Medical Sciences, Tolmar Inc., Zeno Alpha Inc., Accutar Biotechnology Inc, Jiangsu Hansoh Pharmaceutical Co., Ltd., Zenith Epigenetics, Cantargia, BioLite, Inc., PharmAbcine, Ayala Pharmaceuticals, Inc., ERYtech Pharma, SynCore Biotechnology Co., Ltd., Phoenix Molecular Designs, Chipscreen Biosciences, Ltd., OncoTherapy Science, Inc., OncoPep, Inc., and many others.
  • Key HER2 negative Breast Cancer Pipeline Therapies:  BGB-290, OP-1250, AZD9833, Elacestrant, ADG106, H3B-6545, Dato-DXd, HRS8807, TAVO, Mitoxantrone Hydrochloride, Gedatolisib, D-0502, Ipatasertib, ANG1005, Nivolumab, Ipilimumab, Lenvatinib, Onapristone, Xentuzumab, CX-2009, BPI-1178, LY3484356, Afuresertib, Lasofoxifene, ModraDoc006/r, MEDI4736, Infigratinib, SM-88, PQR309, PF-07248144, MCLA-128, SGN-CD228A, RLY-2608, BLU-222, TT-00420, HMPL-013, Zilovertamab vedotin, DAN-222, Niraparib, G1T38, Poziotinib Hydrochloride, EOC202, XZP-3287, RGT-419B, ASTX727, AND019, Lerociclib, SGN-STNV, SCR-6852, NMS-03305293, TOL2506, ZN-c5, AC682, HS-10342, ZEN003694, Nadunolimab, BLEX 404, Olinvacimab, AL101, eryaspase, EndoTAG-1, PMD-026, Chiauranib, OTS167PO, PVX-410, and others.

 

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Table of Contents

  1. Introduction
  2. Executive Summary
  3. HER2 negative Breast Cancer: Overview
  4. HER2 negative Breast Cancer Pipeline Therapeutics
  5. Late Stage HER2 negative Breast Cancer Products (Phase III)
  6. Dato-DXd: Daiichi Sankyo, Inc.
  7. Mid Stage HER2 negative Breast Cancer Products (Phase II)
  8. CX-2009: CytomX Therapeutics
  9. Early Stage Products (Phase I/II)
  10. BPI-1178: Beta Pharma (Suzhou) Co., Ltd.
  11. HER2 negative Breast Cancer Therapeutic Assessment
  12. Inactive HER2 negative Breast Cancer Products
  13. Collaborations Assessment- Licensing / Partnering / Funding
  14. HER2 negative Breast Cancer Unmet Needs
  15. HER2 negative Breast Cancer Market Drivers
  16. HER2 negative Breast Cancer Market Barriers
  17. Appendix
  18. About DelveInsight

 

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About DelveInsight

DelveInsight is a leading Business Consultant and Market Research firm focused exclusively on life sciences. It supports Pharma companies by providing comprehensive end-to-end solutions to improve their performance. It also offers Healthcare Consulting Services, which benefits in market analysis to accelerate business growth and overcome challenges with a practical approach.

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Hereditary Angioedema Market to wintness growth by 2032, Estimates DelveInsight | BioCryst Pharmaceuticals, Ionis Pharmaceuticals, KalVista Pharmaceuticals, CSL Behring, Shire, Pharming Group, Takeda

“Hereditary Angioedema Market”

DelveInsight’s “Hereditary Angioedema Market Insights, Epidemiology, and Market Forecast 2032” report delivers an in-depth understanding of the Hereditary Angioedema, historical and forecasted epidemiology as well as the Hereditary Angioedema market trends in the United States, EU5 (Germany, Spain, Italy, France, and United Kingdom) and Japan.

The Hereditary Angioedema market report also covers emerging drugs, current treatment practices, Hereditary Angioedema market share of the individual therapies, current and forecasted Hereditary Angioedema Market Size from 2019 to 2032 segmented by seven major markets.

 

To know more about the Hereditary Angioedema report offerings, click here: Hereditary Angioedema Market Forecast

 

Some facts of Hereditary Angioedema Market Report

  • According to DelveInsight, Hereditary Angioedema market size is expected to reach USD XX Million by 2032.
  • In 7MM, Hereditary Angioedema market size was USD 2,300 million in 2022.
  • Among all the 7MM, the US consistently captured the highest Hereditary Angioedema market with nearly USD 1,900 million estimated in 2022, which is expected to grow during the forecasted period (2023-2032).
  • Key Hereditary Angioedema Companies: BioCryst Pharmaceuticals, Ionis Pharmaceuticals, KalVista Pharmaceuticals, CSL Behring, Shire, Pharming Group, Takeda Pharmaceuticals, BIOCRYST PHARMACEUTICALS, INC., Attune Pharmaceuticals, Arrowhead Pharmaceuticals, Inc., Adverum Biotechnologies, Inc., CENTOGENE N.V., and Sanofi, and many others.
  • Key Hereditary Angioedema Therapies: Sebetralstat/KVD900, NTLA-2002, BMN 331, Garadacimab, Donidalorsen, STAR-0215, PHA121 (PHA-022121), and others.
  • The diagnosed prevalent cases of HAE in the 7MM varied according to gender, with prevalent cases higher in females than males. Assessments, as per DelveInsight’s analysts, show that the overall diagnosed prevalent cases of HAE in females was 8,500, while it was 5,400 in males in 2022, these cases are subject to rise in the coming years.
  • The Hereditary Angioedema market is expected to surge due to the disease’s increasing prevalence and awareness during the forecast period. Furthermore, launching various multiple-stage Hereditary Angioedema pipeline products will significantly revolutionize the Hereditary Angioedema market dynamics

 

Hereditary Angioedema Overview

Hereditary Angioedema (HAE) is a rare genetic disorder caused by the deficiency in functional C1 inhibitor (C1INH) that results in recurrent attacks of localized subcutaneous or mucosal edema, most commonly affecting the skin, intestines, upper respiratory tract, and oropharynx

HAE is a heterogeneous disease with complex pathophysiology that involves several pathways resulting in the increased production of bradykinin with mutations of multiple molecules in genetic etiology. These could include the Kallikrein gene mutations; Bradykinin gene or its receptor mutations; Kininase 1 gene mutations and loss of function and mutations in gene encoding aminopeptidase and ACE enzymes.

It is classified into three types based on genetic defects such as type I HAE with low levels of C1-INH in the body, type II with poorly functioning C1-INH, or the recently identified types of HAE with normal functioning C1-INH (formerly known as type III HAE). Identification of the novel polymorphisms in several genes leading to modification in the clinical phenotype of HAE is a relatively recent phenomenon. The clinical features of HAE are recurrent and unpredictable spontaneous edema attacks. Traumas, infections, stress, or medical procedures are potential triggers for HAE attacks, and occasionally, angioedema could be associated with prodromal signs, including erythema marginatum.

 

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Key Benefits of Hereditary Angioedema Market Report

  • Hereditary Angioedema market report provides an in-depth analysis of Hereditary Angioedema Market Size, Share, Trend, Epidemiology and Market Forecast till 2030, in 7 major market i.e. EU5 (Germany, Italy, Spain, France and the UK), Japan, and the United States.
  • The Hereditary Angioedema market report will help in developing business strategies by understanding the Hereditary Angioedema Market trends & developments, key players and future market competition that will shape and drive the Hereditary Angioedema market in the upcoming years.
  • The Hereditary Angioedema market report covers Hereditary Angioedema current treatment practices, emerging drugs, market share of the individual therapies in 7 MM.
  • The report provides a detailed assessment of the Hereditary Angioedema market in terms of market drivers & barriers, Unmet Needs, market opportunities, patient population, comparative analysis of pipeline products with detailed clinical profiles, and other factors. 

 

Hereditary Angioedema Market

The landscape of therapeutic options for patients with HAE has changed dramatically in the last two decades. Ongoing research promises even greater change in the foreseeable future. Given the economic and psychosocial burdens for patients living with angioedema, effective therapies with novel mechanisms will offer more choices for patients and physicians, as well as provide greater flexibility in routes of administration. Owing to the launch of upcoming therapies, market size shall increase during forecast period (2019-2032).

The Hereditary Angioedema market outlook section of the report helps to build the detailed comprehension of the historic, current and forecasted Hereditary Angioedema market trends by analyzing the impact of current therapies on the market, unmet needs, drivers and barriers and demand for better technology. 

The report gives a thorough detail of Hereditary Angioedema market trend of each marketed drug and late-stage pipeline therapy by evaluating their impact based on the annual cost of therapy, inclusion and exclusion criteria, mechanism of action, increasing patient pool, covered patient segment, expected launch year, competition with other therapies, and view of the key opinion leaders.

 

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Hereditary Angioedema Epidemiology

The Hereditary Angioedema epidemiology section covers insights about historical and current Hereditary Angioedema patient pool and forecasted trends for every seven major countries (i.e. the United States, EU5 countries (Germany, Spain, Italy, France, and the United Kingdom), and Japan from 2019 to 2032.

It helps to recognize the causes of current and forecasted trends by exploring numerous studies and views of key opinion leaders. The epidemiology section also provides the diagnosed patient pool and their trends along with assumptions undertaken.  

 

Hereditary Angioedema Drugs Uptake and Key Market Players

The Hereditary Angioedema Drugs Uptake section focuses on the rate of uptake of the potential drugs recently launched in the Hereditary Angioedema market or expected to get launched in the market during the study period. The analysis covers Hereditary Angioedema market uptake by drugs; patient uptake by therapies; and sales of each drug.    

Report’s Drugs Uptake section helps in understanding the drugs with the most rapid uptake, reasons behind the maximal use of new drugs and allow the comparison of the drugs on the basis of market share and size which again will be useful in investigating factors important in market uptake and in making financial and regulatory decisions.

Companies are focusing on executing a successful launch that meets the urgent demand for a once-daily oral therapy that will allow HAE patients to live a more normal life. An orally delivered, small molecule offers the opportunity to improve treatment for the disease by making it more convenient for patients to take therapies.

 

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Hereditary Angioedema Companies:

Some of the Hereditary Angioedema companies working in the Hereditary Angioedema Market are BioCryst Pharmaceuticals, Ionis Pharmaceuticals, KalVista Pharmaceuticals, CSL Behring, Shire, Pharming Group, Takeda Pharmaceuticals, BIOCRYST PHARMACEUTICALS, INC., Attune Pharmaceuticals, Arrowhead Pharmaceuticals, Inc., Adverum Biotechnologies, Inc., CENTOGENE N.V., and Sanofi, and many others.

 

Hereditary Angioedema Therapies:

Hereditary Angioedema Drugs Covered are BCX7353, IONIS-PKK-LRx, KVD900, CSL312, and many others.

 

Emerging Hereditary Angioedema drugs Uptake:

  • TAKHZYRO (lanadelumab, Takeda) is a newly-developed monoclonal antibody approved for long-term prophylaxis in HAE patients aged 12 and older. It inhibits plasma kallikrein, preventing the formation of BK and, therefore, decreasing the risk of developing angioedema. Recently, in Feb 2023, the US FDA also approved Takeda’s Takhzyro (lanadelumab-flyo) to prevent HAE attacks in children 2 years of age and older.
  • CINRYZE (Takeda) is an IV human plasma-derived C1-INH approved for patients aged 6 and older. CINRYZE requires IV administration every 3–4 days, and some patients may need higher than typical doses to achieve a reduction in attacks.
  • HAEGARDA (CSL Behring) was approved for long-term prophylaxis for adults and adolescents to fulfill this unmet need. It is a human plasma-derived C1-INH, taken twice weekly as an SC injection. HAEGARDA as a prophylaxis treatment is more effective than CINRYZE and attracted a greater number of patients due to the ease of administration.
  • Potential drug targets include inhibiting factor XII (e.g., with a blocking antibody), plasma kallikrein inhibitor, inhibiting the cleavage of prekallikrein, and blocking the bradykinin-B2-receptor. Along with this, few gene therapies are developing for treating HAE; this will help treat the newly identified mutations such as FXII and PLG HAE.

 

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Table of Content

1. Key Insights

2. Executive Summary 

3. Hereditary Angioedema Competitive Intelligence Analysis

4. Hereditary Angioedema Market Overview at a Glance

5. Hereditary Angioedema Disease Background and Overview

6. Hereditary Angioedema Patient Journey

7. Hereditary Angioedema Epidemiology and Patient Population

8. Hereditary Angioedema Treatment Algorithm, Current Treatment, and Medical Practices

9. Hereditary Angioedema Unmet Needs

10. Key Endpoints of Hereditary Angioedema Treatment

11. Hereditary Angioedema Marketed Products

12. Hereditary Angioedema Emerging Therapies

13. Hereditary Angioedema Seven Major Market Analysis

14. Attribute Analysis

15. Hereditary Angioedema Market Outlook (7 major markets)

16. Hereditary Angioedema Access and Reimbursement Overview

17. KOL Views on the Hereditary Angioedema Market.

18. Hereditary Angioedema Market Drivers

19. Hereditary Angioedema Market Barriers

20. Appendix

21. DelveInsight Capabilities

22. Disclaimer

 

About DelveInsight

DelveInsight is a leading Life Science market research and business consulting company recognized for its off-the-shelf syndicated market research reports and customized solutions to firms in the healthcare sector.

Media Contact
Company Name: DelveInsight Business Research LLP
Contact Person: Ankit Nigam
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Renowned Real Estate Agents in Tucson, AZ, Mark 17 Years of Transformative Service in the Real Estate Market

In the ever-evolving landscape of Tucson’s real estate market, Cheryl and Mark Hepner have stood as beacons of innovation, dedication, and unparalleled service. For 17 years, this dynamic duo has navigated the complexities of buying, selling, and relocating, making a significant impact on the lives of countless individuals and families. Their journey from the Midwest to Tucson in 1999 wasn’t just a move; it was the beginning of a mission to transform the real estate experience for others embarking on similar life-changing paths.

Today, Cheryl and Mark are celebrated not just for their tenure but for the depth of their contribution to the Tucson real estate market. From first-time homebuyers to seasoned investors, the team of Hepners have provided expert guidance through every facet of real estate transactions, including the nuanced areas of short sales and foreclosures.

As one of the top real estate agents in Tucson, AZ, Cheryl’s role as an Associate Broker and Mark’s expertise as a salesperson have created a formidable team. Their approach is deeply personal, born out of their own experience of relocating and starting anew. This empathy and understanding have made them the go-to Realtors in Tucson, AZ, especially for those moving in from out of state. Their ability to connect with clients on a personal level, coupled with their comprehensive knowledge of the market, sets them apart as Tucson, AZ Realtors.

“In real estate, trust and expertise are paramount. Every client’s journey is unique, and understanding that journey is the key to our approach,” says Cheryl Lee Hepner. “Our 17 years in this business have been about more than transactions; they’ve been about building a community and helping people find their place in it.”

For those looking to navigate the complexities of the Tucson real estate market, Cheryl and Mark Hepner offer a blend of experience, empathy, and expertise that is truly unmatched. Their commitment to their clients’ needs and their deep understanding of the market dynamics make them an ideal choice for anyone looking to buy, sell, or relocate in Tucson, AZ. Visit their website at http://www.dreamhomeinaz.com/ for more information.

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Contact Person: Cheryl Hepner
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Phone: +1 520-404-6882
Address:6760 N Oracle Rd #130
City: Tucson
State: Arizona 85704
Country: United States
Website: http://www.dreamhomeinaz.com/

 

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