Month: July 2024

Diffuse Large B-cell Lymphoma Pipeline Insights 2024: Therapies, Clinical Trials, and Clinical Trials by DelveInsight | Biomea Fusion, Autolus Limited, Xynomic Pharma, Hanmi Pharma, S IMV Inc. Seagen

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Diffuse Large B-cell Lymphoma pipeline constitutes 70+ key companies continuously working towards developing 75+ Diffuse Large B-cell Lymphoma treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

“Diffuse Large B-cell Lymphoma Pipeline Insight, 2024“ report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Diffuse Large B-cell Lymphoma Market.

 

The Diffuse Large B-cell Lymphoma 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.

 

Some of the key takeaways from the Diffuse Large B-cell Lymphoma Pipeline Report: 

  • Companies across the globe are diligently working toward developing novel Diffuse Large B-cell Lymphoma treatment therapies with a considerable amount of success over the years. 

  • Diffuse Large B-cell Lymphoma companies working in the treatment market are Ubix Therapeutics, Otsuka Pharmaceutical Co., Ltd, Biomea Fusion Inc, Autolus Limited, Xynomic Pharmaceuticals, Inc., Hanmi Pharmaceutical, S IMV Inc. Seagen Inc., Zai Lab, Genentech, and others, are developing therapies for the Diffuse Large B-cell Lymphoma treatment 

  • Emerging Diffuse Large B-cell Lymphoma therapies in the different phases of clinical trials are- UBX-303, OPB-111077, BMF-219, AUTO3, Abexinostat, Poseltinib, Maveropepimut, Brentuximabvedotin, Odronextamab, Mosunetuzumab, and others are expected to have a significant impact on the Diffuse Large B-cell Lymphoma market in the coming years.  

  • In  June 2024, Pfizer Inc. (NYSE: PFE) reported detailed overall survival (OS) results from the Phase 3 ECHELON-3 study of ADCETRIS® (brentuximab vedotin) combined with lenalidomide and rituximab for relapsed/refractory diffuse large B-cell lymphoma (DLBCL). The study indicated that this combination reduced the risk of death by 37% compared to a placebo combined with lenalidomide and rituximab (HR 0.63 [95% CI: 0.445-0.891], p=0.0085). The OS benefit was consistent across all levels of CD30 expression. These results will be presented as a late-breaking abstract (LBA7005) at the 2024 American Society of Clinical Oncology (ASCO) Annual Meeting, alongside four-year results from the Phase 3 HD21 trial in advanced classical Hodgkin lymphoma (cHL) (LBA7000).

  • In April 2024, Roche has disclosed findings from the Phase III STARGLO trial demonstrating that its treatment Columvi (glofitamab), in combination with gemcitabine and oxaliplatin (GemOx), enhanced overall survival (OS) in patients with relapsed or refractory (R/R) diffuse large B-cell lymphoma (DLBCL). This multicenter, open-label, randomized study evaluated the safety and effectiveness of Columvi plus GemOx versus MabThera/Rituxan (rituximab) combined with GemOx.

  • In March 2024, GenFleet Therapeutics has entered into a clinical trial collaboration and supply agreement with BeiGene Switzerland to initiate a Phase Ib/II clinical trial combining GFH009 and BRUKINSA (zanubrutinib) for the treatment of diffuse large B cell lymphoma (DLBCL). GFH009 is a cyclin-dependent kinase 9 (CDK9) inhibitor developed by GenFleet, while BRUKINSA is a Bruton’s tyrosine kinase (BTK) inhibitor from BeiGene.

  • In Aug23, Prelude Therapeutics is doing clinical testing on PRT-2527, which is now in Phase I for Diffuse Large B-Cell Lymphoma. GlobalData estimates that a 78% phase transition success rate (PTSR) indication threshold is required for Phase I medications for diffuse large B-cell lymphoma to advance to Phase II.

 

Diffuse Large B-cell Lymphoma Overview

Diffuse Large B-cell Lymphoma (DLBCL) is a type of non-Hodgkin lymphoma, which is a cancer that originates in the lymphatic system. DLBCL specifically affects B-cells, a type of white blood cell crucial for the immune system. It is called “diffuse” because the cancerous B-cells grow rapidly and can spread throughout the lymphatic system and sometimes beyond.

 

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Emerging Diffuse Large B-cell Lymphoma Drugs Under Different Phases of Clinical Development Include:

  • UBX-303: Ubix Therapeutics

  • OPB-111077: Otsuka Pharmaceutical Co., Ltd

  • BMF-219: Biomea Fusion Inc

  • AUTO3: Autolus Limited

  • Abexinostat: Xynomic Pharmaceuticals, Inc.

  • Poseltinib: Hanmi Pharmaceutical

  • Maveropepimut: S IMV Inc.

  • Brentuximabvedotin: Seagen Inc.

  • Odronextamab: Zai Lab

  • Mosunetuzumab: Genentech

 

Diffuse Large B-cell Lymphoma Route of Administration

Diffuse Large B-cell Lymphoma 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.

  • Molecule Type

 

Diffuse Large B-cell Lymphoma Molecule Type

Diffuse Large B-cell Lymphoma Products have been categorized under various Molecule types, such as

  • Monoclonal Antibody

  • Peptides

  • Polymer

  • Small molecule

  • Gene therapy

  • Product Type

 

Diffuse Large B-cell Lymphoma Pipeline Therapeutics Assessment

  • Diffuse Large B-cell Lymphoma Assessment by Product Type

  • Diffuse Large B-cell Lymphoma By Stage and Product Type

  • Diffuse Large B-cell Lymphoma Assessment by Route of Administration

  • Diffuse Large B-cell Lymphoma By Stage and Route of Administration

  • Diffuse Large B-cell Lymphoma Assessment by Molecule Type

  • Diffuse Large B-cell Lymphoma by Stage and Molecule Type

 

DelveInsight’s Diffuse Large B-cell Lymphoma Report covers around 75+ 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 Diffuse Large B-cell Lymphoma product details are provided in the report. Download the Diffuse Large B-cell Lymphoma pipeline report to learn more about the emerging Diffuse Large B-cell Lymphoma therapies

 

Some of the key companies in the Diffuse Large B-cell Lymphoma Therapeutics Market include:

Key companies developing therapies for Diffuse Large B-cell Lymphoma are – AstraZeneca, Bristol-Myers Squibb, Seattle Genetics/Takeda, ADC Therapeutics, SymBio Pharmaceuticals, Denovo Biopharma, Merck, Amgen, TG Therapeutics, Bayer and others.

 

Diffuse Large B-cell Lymphoma Pipeline Analysis:

The Diffuse Large B-cell Lymphoma pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Diffuse Large B-cell Lymphoma 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 Diffuse Large B-cell Lymphoma Treatment.

  • Diffuse Large B-cell Lymphoma key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.

  • Diffuse Large B-cell Lymphoma 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 Diffuse Large B-cell Lymphoma 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 Diffuse Large B-cell Lymphoma drugs and therapies

 

Diffuse Large B-cell Lymphoma Pipeline Market Drivers

  • Increasing Prevalence of DLBCL, increased research and development and CAR-T therapies are some of the important factors that are fueling the Diffuse Large B-cell Lymphoma Market.

 

Diffuse Large B-cell Lymphoma Pipeline Market Barriers

  • However, high cost of treatment, aggressive disease biology and geriatric vulnerability and other factors are creating obstacles in the Diffuse Large B-cell Lymphoma Market growth.

 

Scope of Diffuse Large B-cell Lymphoma Pipeline Drug Insight    

  • Coverage: Global

  • Key Diffuse Large B-cell Lymphoma Companies: Ubix Therapeutics, Otsuka Pharmaceutical Co., Ltd, Biomea Fusion Inc, Autolus Limited, Xynomic Pharmaceuticals, Inc., Hanmi Pharmaceutical, S IMV Inc. Seagen Inc., Zai Lab, Genentech, and others

  • Key Diffuse Large B-cell Lymphoma Therapies: UBX-303, OPB-111077, BMF-219, AUTO3, Abexinostat, Poseltinib, Maveropepimut, Brentuximabvedotin, Odronextamab, Mosunetuzumab, and others

  • Diffuse Large B-cell Lymphoma Therapeutic Assessment: Diffuse Large B-cell Lymphoma current marketed and Diffuse Large B-cell Lymphoma emerging therapies

  • Diffuse Large B-cell Lymphoma Market Dynamics: Diffuse Large B-cell Lymphoma market drivers and Diffuse Large B-cell Lymphoma market barriers 

 

Request for Sample PDF Report for Diffuse Large B-cell Lymphoma Pipeline Assessment and clinical trials

 

Table of Contents 

1. Diffuse Large B-cell Lymphoma Report Introduction

2. Diffuse Large B-cell Lymphoma Executive Summary

3. Diffuse Large B-cell Lymphoma Overview

4. Diffuse Large B-cell Lymphoma- Analytical Perspective In-depth Commercial Assessment

5. Diffuse Large B-cell Lymphoma Pipeline Therapeutics

6. Diffuse Large B-cell Lymphoma Late Stage Products (Phase II/III)

7. Diffuse Large B-cell Lymphoma Mid Stage Products (Phase II)

8. Diffuse Large B-cell Lymphoma Early Stage Products (Phase I)

9. Diffuse Large B-cell Lymphoma Preclinical Stage Products

10. Diffuse Large B-cell Lymphoma Therapeutics Assessment

11. Diffuse Large B-cell Lymphoma Inactive Products

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

13. Diffuse Large B-cell Lymphoma Key Companies

14. Diffuse Large B-cell Lymphoma Key Products

15. Diffuse Large B-cell Lymphoma Unmet Needs

16 . Diffuse Large B-cell Lymphoma Market Drivers and Barriers

17. Diffuse Large B-cell Lymphoma Future Perspectives and Conclusion

18. Diffuse Large B-cell Lymphoma 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.

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To view the original version on ABNewswire visit: Diffuse Large B-cell Lymphoma Pipeline Insights 2024: Therapies, Clinical Trials, and Clinical Trials by DelveInsight | Biomea Fusion, Autolus Limited, Xynomic Pharma, Hanmi Pharma, S IMV Inc. Seagen

In-Vitro Diagnostics (IVD) Market to Flourish Notably with a 5.3% CAGR through 2031; Introduction of Personalized Medicine to Help Growth

“Skyquest Technology”
In-Vitro Diagnostics Market Size, Share, Growth Analysis, By Product type(Instrument & Reagent (Instruments, Reagents [By Raw Material {Antigen-antibody, Enzyme & Substrate, Primers & Probe), By Technology(Immunoassays (Enzyme-Linked Immunosorbent Assays (ELISA), Chemiluminescence immunoassays, Immunofluorescence assays, Rapid tests), By Specimen(Blood, CSF, Urine, Blood Fluid), By Test Type(Laboratory Tests, Point-Of-Care Tests), By Region – Industry Forecast 2024-2031

In-vitro Diagnostics (IVD) Market size was valued at USD 83.50 billion in 2022 and is poised to grow from USD 87.93 billion in 2023 to USD 132.90 billion by 2031, growing at a CAGR of 5.3% during the forecast period (2024-2031).

In-Vitro Diagnostics market is undergoing an intense transformation driven by innovations and a steady commitment to improve healthcare. In the past few years, the industry experienced plenty of improvements mainly in domains like molecular diagnostics, genomics, the IVD space, and software solution levels, during the pandemic. Moreover, increased demand for superior testing techniques and the rising number of chronic patients to considerably impact in-Vitro Diagnostics.

The COVID-19 pandemic has significantly supported the improvements in the PCR (polymerase chain reaction) testing. It can quickly deliver results with the same test sample for various findings. The improvement of condition-specific tests and markers, the rising importance of companion diagnostics, and POC (point-of-care) testing with multiplexing competences are all expected to experience remarkable growth soon. Furthermore, Liquid Biopsy is one such key area that is heavily demanding the use of IVD technologies, wherein it offers a painless approach, allowing diagnosis of disease based on urine and blood samples. Mass spectrometry is yet another technique applied in the study of omics and is regarded as ‘diagnostics future’. This technology delivers femtomolar sensitivity, high-throughput, and quick testing, taking the study from molecular levels to cellular levels. These advancements cut across all the areas of application.

Download a detailed overview:

https://www.skyquestt.com/sample-request/in-vitro-diagnostics-market

Growing Trend of Point-of-Care Testing Projected to Majorly Transform Market

IVDs (in-vitro diagnostics) are vital resources in healthcare that inform nearly 70% of all medical decisions throughout the disease detection and monitoring of the patient’s overall health. Further, the advancements in genomics and IVDs are taking the diagnostics to the next level. Physicians are currently using refined assays physicians to help them screen for cancer-like severe diseases at an early stage, where symptoms do not exist, and cure rates are higher. Prognostic and predictive biomarkers are remarkably growingin prominence. With biomarkers assisting the doctors in various stages of a patient’s treatment, scientists are exploring a novel model called ‘precision medicine’, wherein doctors can select the right treatment for the right patient. Another major trend seen in the in-vitro diagnostics domain is the growth of POCT (point-of-care testing), usually performed near the patient like his home or the doctor’s clinic. POCT offers comparatively quick turnaround times and is reasonably priced. Microfluidics is another evolving technology holding the potential to address the challenges of the previously used methodologies. They are the miniaturized tools that control the fluids through reagents series. They are also regarded as lab-on-a-chip owing to their ability to incorporate multiple laboratory functions on one integrated circuit.

Request Free Customization of this report:

https://www.skyquestt.com/speak-with-analyst/in-vitro-diagnostics-market

  • In May 2024, Danaher Corporation agreed to a partnership with Johns Hopkins University. The partnership aims to develop novel techniques for diagnosing mild (TBI) Traumatic Brain Injury. Belonging to the Danaher Beacons program, the analysts at the University will leverage expertise from the Beckman Coulter Diagnostics, a subsidiary of Danaher and front-runner in clinical diagnostics, to establish correlations between clinical outcomes and a novel biomarker panel.
  • In May 2022, Becton, Dickinson and Company, a lead medical technology company, announced a novel high-throughput molecular diagnostic amalgamation test for Influenza A/B and SARS-CoV-2, the second test accessible for the BD COR™ PX/MX System is expected to be CE marked to the in-vitro diagnostics directive 98/79/EC.
  • In May 2024, bioMérieux, a leader in in-vitro diagnostics, announced the U.S. FDA 510(k) authorization of VIDAS® TBI (GFAP, UCH-L1). This is a serum-based test that supports the examination of patients with mild (mTBI) traumatic brain injury, comprising concussion. The assay incorporates a distinctive combination of the biomarkers UCH-L1* and GFAP, proteins that go in circulation after cellular injury.
  • In May 2022, Sysmex gathered evidence through collaborative research in partnership with Key Opinion Leaders (KOLs). To expand clinical applications, the company has been focusing on regulatory compliance for the common reagents and analyzers that are used with these assay kits. The company recently announced conformism to the European IVD regulation for these common analyzers and reagents.

 

View report summary and Table of Contents (TOC):

https://www.skyquestt.com/report/in-vitro-diagnostics-market

The in-vitro diagnostics market is anticipated to witness more major transformations with substantial growth by 2024. Trends like personalized medicine, POCT, digital diagnostics, machine learning& AI in diagnostics, liquid biopsy, and more hold promises for better overall patient improvement, lower cost, and transform the delivery of medical services.

Related Reports:

Quantum Computing Market

Visit Our Website: https://www.skyquestt.com/

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Senpex Technology Launches Intuitive New Mobile App to Provide a Streamlined Last-Mile Delivery Experience to a Wide Range of Users

San Jose, CA – July 9, 2024 – Senpex Technology, a logistics and delivery service that utilizes groundbreaking technology to provide the fastest and most efficient last-mile delivery resource for businesses, announced today the release of an updated mobile app that gives users access to its comprehensive suite of logistics services in an enhanced, user-friendly interface.

“Customers seeking last-mile logistics services in the modern marketplace have complex needs that demand a comprehensive suite of services,” says Anar Mammadov, co-founder and CEO of Senpex Technologies. “They need to be able to do much more than simply select a drop-off or pick-up. They want extra services, such as specialized vehicles or set-up upon delivery. Senpex understands that, so we are giving them a convenient and intelligent way to access those services.”

Senpex’s new app combines the insights gained from extensive customer feedback with the decades of experience the company has with developing technology to deliver an unparalleled solution to last-mile delivery needs. The app focuses on providing the three most popular logistics requests Senpex receives: last-mile, commercial moving, and nationwide. With each option, users are guided through an easy-to-navigate interface that allows them to provide an expanded list of details. No detail is overlooked by Senpex, which means every delivery, whether it is sent across town or across the country, can be processed with excellence.

“Prior to this update, our clients had to visit our website to gain access to the full suite of Senpex services,” Mammadov explains. “Now, they can gain access to an enhanced number of options via the app. If they need a larger vehicle or extra delivery helpers to facilitate large items, they can easily request it through the app. From pricing a pickup to confirming a delivery, everything can be done from wherever you are via the app.”

The new Senpex app also offers enhanced efficiency by enabling users to receive a detailed quote for the services they need before entering any personal information or establishing an account. Once an account is established, the app allows users to keep track of their “in progress,” “completed,” and “repetitive” orders with a simple tap. If issues occur, users can use the app to connect with a driver or customer support representative. 

Essentially, Senpex’s new app provides every user with their own personal shipping expert. Mammadov anticipates the app will be welcomed by B2B shippers, whose logistics needs are more complicated.

“Most businesses look to mobile services for basic deliveries, but shift to more cumbersome browser-based interfaces when things get complicated,” Mammadov shares. “With the new Senpex app, you can stay mobile for everything — no matter how complicated — and once you place a delivery order, the app keeps you continuously updated on your progress. Shippers no longer need to sit at their desks waiting for news that their delivery is complete. The Senpex app keeps them conveniently informed wherever they are, showing real-time tracking and live notifications.”

Last-mile logistics is one of the most in-demand and costly services in today’s global marketplace, with e-commerce needs driving the volume of deliveries higher on a daily basis. Senpex was established in 2017 to provide a more reliable and cost-effective solution for the growing number of businesses seeking to provide on-demand delivery. One of the keys to Senpex’s success has been leveraging the power of technology to bring heightened levels of efficiency to delivery routing, customer service, and driver management automation.

The new Senpex International app is now available for free download in all major app stores in both Android and IOS versions.

About Senpex

Senpex is an on-demand delivery platform specialized in providing last-mile logistics services via mobile apps, All-in-One Smart Portal, and Advanced Senpex API — a customized integrated delivery option that automates logistics needs and helps businesses scale businesses to new locations. Senpex’s AI-based framework enables its technology to deploy a unique set of custom parameters for each corporate client, providing personalized solutions that make shipping more affordable and convenient for businesses of all sizes.

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Helicobacter Pylori Infections Pipeline 2024: Clinical Trials Assessment, FDA Approvals, Therapies, Involved by DelveInsight | Phathom Pharma, HK inno.N Corporation, Elpen Pharma, Deva Holding

(Las Vegas, Nevada, United States) As per DelveInsight’s assessment, globally, Helicobacter Pylori Infections pipeline constitutes 5+ key companies continuously working towards developing 5+ Helicobacter Pylori Infections treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

“Helicobacter Pylori Infections Pipeline Insight, 2024“ report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Helicobacter Pylori Infections Market.

 

The Helicobacter Pylori Infections 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.

 

Some of the key takeaways from the Helicobacter Pylori Infections Pipeline Report: 

  • Companies across the globe are diligently working toward developing novel Helicobacter Pylori Infections treatment therapies with a considerable amount of success over the years. 

  • Helicobacter Pylori Infections companies working in the treatment market are Servatus Biopharmaceuticals, TenNor Therapeutics (Suzhou) Limited, Phathom Pharmaceuticals, Inc., HK inno.N Corporation, Elpen Pharmaceutical Co. Inc., Deva Holding A.S., Lallemand Health Solutions, Takeda, Meridian Bioscience, Inc., Janssen Cilag Pharmaceutica S.A.C.I., Greece, RedHill Biopharma Limited, Il-Yang Pharm. Co., Ltd., Asan Medical Center, MerLion Pharmaceuticals GmbH, TenNor Therapeutics (Suzhou) Limited, and others, are developing therapies for the Helicobacter Pylori Infections treatment 

  • Emerging Helicobacter Pylori Infections therapies in the different phases of clinical trials are- SVT1C4610, TNP-2198, Vonoprazan, Tegoprazan, Esomeprazole, Levofloxacin, Lacidofil, CJ-12420/Clarithromycin/AmoxicillinVonoprazan, Vonoprazan, Lansoprazole (Lanton), rabeprazole sodium, RHB-105, Ilaprazole + Amoxicillin, pantoprazole, Finafloxacin + Amoxicillin, Rifasutenizol capsules, and others are expected to have a significant impact on the Helicobacter Pylori Infections market in the coming years.   

  • In May 2022, Biomerica, Inc. announced CE Mark for its hp+detect diagnostic test that detects Helicobacter pylori bacteria. The company will begin to market and sell its hp+detect diagnostic test in the European Union (EU) and other international countries following the registration of the product in each country in which it is sold. Source: https://www.mordorintelligence.com/industry-reports/helicobacter-pylori-diagnostics-market

  • Bio-Rad launched Platelia H. Pylori IgG, an immuno-enzymatic assay for qualitative determination of IgG antibodies, in July 2022. Serology is a non-invasive, delicate, and straightforward technique for identifying H. pylori infection. The Platelia H. Pylori IgG immunoenzymatic assay is used to determine the quality of IgG antibodies.

 

Helicobacter Pylori Infections Overview

Helicobacter pylori (H. pylori) is a type of bacteria that infects the stomach lining and can cause various gastrointestinal issues. It is a common infection, affecting about half of the world’s population. H. pylori infections are usually acquired during childhood and can persist for many years if left untreated. 

 

Get a Free Sample PDF Report to know more about Helicobacter Pylori Infections Pipeline Therapeutic Assessment-

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Emerging Helicobacter Pylori Infections Drugs Under Different Phases of Clinical Development Include:

  • SVT1C4610: Servatus Biopharmaceuticals

  • TNP-2198: TenNor Therapeutics (Suzhou) Limited

  • Vonoprazan: Phathom Pharmaceuticals, Inc.

  • Tegoprazan: HK inno.N Corporation

  • Esomeprazole: Elpen Pharmaceutical Co. Inc.

  • Levofloxacin: Deva Holding A.S.

  • Lacidofil: Lallemand Health Solutions

  • CJ-12420/Clarithromycin/AmoxicillinVonoprazan: HK inno.N Corporation

  • Vonoprazan: Takeda

  • Lansoprazole (Lanton): Meridian Bioscience, Inc.

  • rabeprazole sodium: Janssen Cilag Pharmaceutica S.A.C.I., Greece

  • RHB-105: RedHill Biopharma Limited

  • Ilaprazole + Amoxicillin: Il-Yang Pharm. Co., Ltd.

  • pantoprazole: Asan Medical Center

  • Finafloxacin + Amoxicillin: MerLion Pharmaceuticals GmbH

  • Rifasutenizol capsules: TenNor Therapeutics (Suzhou) Limited

 

Helicobacter Pylori Infections Route of Administration

Helicobacter Pylori Infections 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

 

Helicobacter Pylori Infections Molecule Type

Helicobacter Pylori Infections Products have been categorized under various Molecule types, such as

  • Monoclonal Antibody

  • Peptides

  • Polymer

  • Small molecule

  • Gene therapy 

 

Helicobacter Pylori Infections Pipeline Therapeutics Assessment

  • Helicobacter Pylori Infections Assessment by Product Type

  • Helicobacter Pylori Infections By Stage and Product Type

  • Helicobacter Pylori Infections Assessment by Route of Administration

  • Helicobacter Pylori Infections By Stage and Route of Administration

  • Helicobacter Pylori Infections Assessment by Molecule Type

  • Helicobacter Pylori Infections by Stage and Molecule Type

 

DelveInsight’s Helicobacter Pylori Infections Report covers around 5+ 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 Helicobacter Pylori Infections product details are provided in the report. Download the Helicobacter Pylori Infections pipeline report to learn more about the emerging Helicobacter Pylori Infections therapies

 

 

Some of the key companies in the Helicobacter Pylori Infections Therapeutics Market include:

Key companies developing therapies for Helicobacter Pylori Infections are – Takeda Pharmaceutical, AbbVie, Cumberland Pharmaceuticals, Eisai Co, Bio-Rad Laboratories, F. Hoffmann-La, Roche, Alpha Laboratories, Biohit, Biomerica, Inc., QuickNaviTM, and others.

 

Helicobacter Pylori Infections Pipeline Analysis:

The Helicobacter Pylori Infections pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Helicobacter Pylori Infections 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 Helicobacter Pylori Infections Treatment.

  • Helicobacter Pylori Infections key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.

  • Helicobacter Pylori Infections 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 Helicobacter Pylori Infections 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 Helicobacter Pylori Infections drugs and therapies

 

Scope of Helicobacter Pylori Infections Pipeline Drug Insight    

  • Coverage: Global

  • Key Helicobacter Pylori Infections Companies: Servatus Biopharmaceuticals, TenNor Therapeutics (Suzhou) Limited, Phathom Pharmaceuticals, Inc., HK inno.N Corporation, Elpen Pharmaceutical Co. Inc., Deva Holding A.S., Lallemand Health Solutions, Takeda, Meridian Bioscience, Inc., Janssen Cilag Pharmaceutica S.A.C.I., Greece, RedHill Biopharma Limited, Il-Yang Pharm. Co., Ltd., Asan Medical Center, MerLion Pharmaceuticals GmbH, TenNor Therapeutics (Suzhou) Limited, and others

  • Key Helicobacter Pylori Infections Therapies: SVT1C4610, TNP-2198, Vonoprazan, Tegoprazan, Esomeprazole, Levofloxacin, Lacidofil, CJ-12420/Clarithromycin/AmoxicillinVonoprazan, Vonoprazan, Lansoprazole (Lanton), rabeprazole sodium, RHB-105, Ilaprazole + Amoxicillin, pantoprazole, Finafloxacin + Amoxicillin, Rifasutenizol capsules, and others

  • Helicobacter Pylori Infections Therapeutic Assessment: Helicobacter Pylori Infections current marketed and Helicobacter Pylori Infections emerging therapies

  • Helicobacter Pylori Infections Market Dynamics: Helicobacter Pylori Infections market drivers and Helicobacter Pylori Infections market barriers 

 

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Table of Contents

1. Helicobacter Pylori Infections Report Introduction

2. Helicobacter Pylori Infections Executive Summary

3. Helicobacter Pylori Infections Overview

4. Helicobacter Pylori Infections- Analytical Perspective In-depth Commercial Assessment

5. Helicobacter Pylori Infections Pipeline Therapeutics

6. Helicobacter Pylori Infections Late Stage Products (Phase II/III)

7. Helicobacter Pylori Infections Mid Stage Products (Phase II)

8. Helicobacter Pylori Infections Early Stage Products (Phase I)

9. Helicobacter Pylori Infections Preclinical Stage Products

10. Helicobacter Pylori Infections Therapeutics Assessment

11. Helicobacter Pylori Infections Inactive Products

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

13. Helicobacter Pylori Infections Key Companies

14. Helicobacter Pylori Infections Key Products

15. Helicobacter Pylori Infections Unmet Needs

16 . Helicobacter Pylori Infections Market Drivers and Barriers

17. Helicobacter Pylori Infections Future Perspectives and Conclusion

18. Helicobacter Pylori Infections 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.

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Hydrogen Peroxide Market to Shoot Astonishingly with an Outstanding 5.01% CAGR through 2031

“Skyquest Technology”
Hydrogen Peroxide Market Size, Share, Growth Analysis, By Function(Disinfectant, Bleaching, Oxidant, and Others), By Grade(90% H2O2, 35% H2O2, 6 TO 10% H2O2, 3% H2O2), By Application(Chemical Synthesis, Bleaching, Disinfectant, Cleaning and Etching), By End-use Industry(Pulp & Paper (Chemical Pulp, Mechanical Pulp, Recycled Pulp), Food & Beverages (Sterilization), By Region – Industry Forecast 2024-2031

Hydrogen Peroxide Market size was valued at USD 3.16 billion in 2022 and is poised to grow from USD 3.32 billion in 2023 to USD 4.90 billion by 2031, growing at a CAGR of 5.01% during the forecast period (2024-2031). 

The global Hydrogen Peroxide market is widely used in the bleaching of paper and pulp. Also, it is easily accessible and prominently used as a topical antiseptic. Nonetheless, hydrogen peroxide is a highly versatile chemical with several uses and is capable of much wider applications. Its increasing applications as an antiseptic in the healthcare sector and consumer disinfecting in cleaning several products are fuelling its demand.

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Hydrogen peroxide is currently being used in novel applications in semiconductor, metal extraction, mining, and agriculture industries. The chemical substance holds a strong oxidizing impact. The beneficial quality majorly supported its use in cosmetics. In addition, hydrogen peroxide 35% is among the highly popular substances used in the making of cleaning chemicals. The chemical is extremely corrosive on the living tissues, due to which it is majorly used in chemicals for disinfection and cleaning. The chemical also holds applications in the food and construction industries. It supports the cleaning of surfaces and eliminates impurities like ventilation ducts and sewer pipes. In most household applications, the chemical is found in the 3% safe solution. Treating wounds and disinfection uses are among the key applications in households. Furthermore, pharmaceutical uses can also be added to its application.

Focus on Delivering High-Performing & Innovative Products to Strengthen the Market Competition

Hydrogen peroxide will witness continued growth in the near future owing to expanding demand for innovative and sustainable products, and also broader implementation of technology. The market players are seeing the potential to drive the industry growth via numerous strategies. They can emphasize delivering high-performing and innovative products, leveraging the improvements in the technology. Moreover, players in the market avail the benefit of expanding their channels of distribution to target new clients. Also, collaborations and strategic associations can be achieved to strengthen presence and improve competitiveness. Besides these applications, there are upcoming applications as well that will further increase the product’s demand. A novel process can help produce hydrogen peroxide with greater selectivity, leading to 94% hydrogen peroxide and comparatively less water. Vaporized form of hydrogen peroxide, abbreviated as VHP holds higher antimicrobial efficacy as compared to liquid and can penetrate diffusion-restricted surroundings. In agricultural applications, diluted alkaline treatment of crop remains like corn cobs, wheat straw, and cornstalks can improve their nutrition for cattle.

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  • In April 2024, Evonik launched H2O2 (carbon-neutral hydrogen peroxide) to its clients in Europe. The product was sold with a “Way to GO2” permit, which denotes Evonik’s Vigorous Oxygens business line’s strategy for sustainability from 2022.
  • In 2024 March, Solvay declared that it was postponing the construction of a hydrogen peroxide (electronics-grade) plant near Phoenix Arizona. The company mentioned the current status of semiconductor manufacturing market dynamics and federal subsidies as the reasons behind the delay.
  • Arkema company declares a price increase of its Sodium Chlorate and Hydrogen Peroxide. Effective from 2021 October, Arkema will increase its cost across its Sodium Chlorate and Hydrogen Peroxide ranges in Europe and for the export markets by 15 percent.
  • On April 10 2024, Mitsubishi Gas Chemical Company (Head Office: Chiyoda-ku, Tokyo; President: Masashi Fujii) planned the expansion of the Texas Plant of (MPCA) MGC Pure Chemicals America, Incorporation. (MPCA has its headquarters in Arizona, in the USA), a merged subsidiary that produces and markets super-pure ammonium hydroxide and super-pure hydrogen peroxide for use during the semiconductors’ manufacturing processes.

 

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In conclusion, constant R&D efforts in Vaporized Hydrogen Peroxide sterilization cycle techniques hold abundant potential for improving purification of reusable medical devices. By dealing with the challenges associated with the penetration of hydrogen peroxide in diffusion-limited surroundings, such as lumens, scientists can propel significant advancements in the results of sterilization and support the progressions in the domain.

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Green Chemicals Market Surging at a CAGR of 8.27% through 2031 Fuelled by High Demand for Environment Friendly Products

“Skyquest Technology”
Green Chemicals Market Size, Share, Growth Analysis, By Type(Bio-Alcohols (Bio-Ethanol, Bio-Butanol, Bio-Methanol, Others)), By Application(Industrial & Chemical, Food & Beverages, Pharmaceuticals, Packaging), By Region – Industry Forecast 2024-2031

Green Chemicals Market size was valued at USD 35.49 Billion in 2022 and is poised to grow from USD 38.43 Billion in 2023 to USD 72.56 Billion by 2031, growing at a CAGR of 8.27% in the forecast period (2024-2031).

Key players in the global green chemical market have started focusing on using bio-based materials in their manufacturing processes from the past couple of years. This change was possible due to the significant shift in the global market away from conventional chemical sources towards sustainable solutions derived from renewable resources. These green chemicals are used in many industries like construction, automotive, packaging, and agriculture because of this change towards environmental products.

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Green chemicals, also known as bio-based chemicals, are ecologically friendly and renewable substances derived mostly from bio-based raw materials. These components are sourced from plants, vegetables, and animals. Vegetable oils, animal fats, sugar, starch, bioethanol, corn, sugarcane, wheat, cassava, and other plants are significant suppliers of these bio-chemicals. Chemicals derived from biomaterials, compared to those derived from petroleum, are more environmentally friendly. They are designed to minimize their influence on recycling, disposal, transportation, installation, processing, and manufacture, thereby helping to maintain ecological balance. The utilization of green chemical manufacturing in several industries has effectively reduced the generation of harmful compounds. 

Customer Demand for Sustainable Products is Surging the Green Chemicals Market Growth

Recently, the demand for environmentally friendly products has seen a rise because customers are ready to invest more for sustainable alternatives. Today most of the consumers worldwide are willing to invest more towards sustainable companies. This percentage is particularly elevated among specific customer demographics. For instance, sustainability is a primary factor that influences the shopping decisions of 66% of all buyers and 75% of millennial shoppers. As eco-friendly products are gaining more popularity in the market the opportunities for the manufacturers of green chemical also increases. Therefore, it has become crucial for chemical companies to focus on sustainability if they want to take advantage of the increasing customer demand.

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High Investment in Research & Development is Driving the Adoption of Environmentally Friendly Chemicals

Government bodies and private institutions are investing heavily on the research and development of green chemicals. The research will help in understanding the many ways in which the chemical can be used in various sectors like textile. Expansion in the usage of this green chemical will also help in bringing sustainability across several industries. For instance, DowDupont, a market leader in chemical manufacturing is focusing on extending its product range in advanced materials and agriculture. The business is investing more for R&D in biomaterials to satisfy customer demands.

  • In January 2024, NTPC Limited went into a non-binding MoU agreement with Numaligarh Refinery Limited for bio-refinery projects. This partnership will also help them to achieve the net-zero targets.
  • In September 2022, RiKarbon Inc. established a cooperation with BASF to create bio-based emollients. RiKarbon’s patented technology will help the personal care sector to find sustainable solutions. They can recycle bio-waste into bio-based, biodegradable emollients.
  • In June 2022, JSW Cement Limited introduced an eco-friendly construction chemical product.These can help inpreserving natural resources and even lower landslides, floods, and air pollution.
  • In May 2022, Cellulose Solutions’ subsidiary Verdant Innovations introduced its initial collection of specialty green sustainable chemicals. The business will focus on items like hemp, pulp, textile, and nonwovens.

 

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The green chemicals industry has experienced substantial expansion in recent times due to the increasing use of packaging materials derived from renewable sources, such as plant and animal waste. Bio-based packaging is good for the environment because they are non-toxic materials. These packaging’s are also cost-efficient and can be easily disposed. In the next few years, the green chemical market will see a significant growth due to increasing public awareness and high demand for sustainable products creating a circular bioeconomy.

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Interstitial Lung Disease Pipeline Analysis 2024: FDA Approvals, Clinical Trials, Therapies, Mechanism of Action, Route of Administration, Companies by DelveInsight

“Interstitial Lung Disease Pipeline”
Interstitial Lung Disease companies are AdAlta, Bristol-Myers Squibb, aTyr Pharma, Avalyn Pharmaceuticals, Beijing Continent Pharmaceutical, Regend Therapeutics, Reata Pharmaceuticals, FibroGen, Genentech, Boehringer Ingelheim, Prometheus Biosciences, HEC Pharm, Bayer, Insmed, Bristol-Myers Squibb, Avalyn Pharma, PureTech Health, Roche, Ark Biosciences, Novartis, Kadmon Pharmaceuticals, GenKyoTex, Taiho Pharmaceutical,Syndax Pharmaceuticals, CSL Behring and AstraZeneca, and others.

(Albany, United States) As per DelveInsight’s assessment, globally, Interstitial Lung Disease pipeline constitutes 120+ key companies continuously working towards developing 120+ Interstitial Lung Disease treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

“Interstitial Lung Disease Pipeline Insight, 2024″ report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Interstitial Lung Disease Market.

The Interstitial Lung Disease 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.

 

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Some of the key takeaways from the Interstitial Lung Disease Pipeline Report:

  • Interstitial Lung Disease Companies across the globe are diligently working toward developing novel Interstitial Lung Disease treatment therapies with a considerable amount of success over the years. 
  • Interstitial Lung Disease companies working in the treatment market are AdAlta, Bristol-Myers Squibb, aTyr Pharma, Avalyn Pharmaceuticals, Beijing Continent Pharmaceutical, Regend Therapeutics, Reata Pharmaceuticals, FibroGen, PureTech Health, Bellerophon Pulse Technologies, OncoArendi Therapeutics, LTT Bio-Pharma, EmphyCorp, Genentech, Cudetaxestat, Boehringer Ingelheim, Prometheus Biosciences, HEC Pharm, Bayer, Insmed, Bristol-Myers Squibb, Avalyn Pharma, PureTech Health, Roche, Ark Biosciences, Novartis, Lung Therapeutics, Horizon, MediciNova, Endeavor BioMedicines, Pliant Therapeutics,  Kadmon Pharmaceuticals, GenKyoTex, Taiho Pharmaceutical,Syndax Pharmaceuticals, Metagone Biotech, Galecto Biotech, CSL Behring and AstraZeneca, and others are developing therapies for the Interstitial Lung Disease treatment.
  • Emerging Interstitial Lung Disease therapies such as AD-214, Abatacept, ATYR1923, Pirfenidone inhalation, RO-0220912, Lung stem cells, Bardoxolone methyl, Pamrevlumab, Deupirfenidone, INOpulse, OATD 01, LT 0011, GDC 3280,  Blade Therapeutics, BI 1015550, PRA 023, Yifenidone, Riociguat, Treprostinil Palmitil, BMS 986278, Pirfenidone inhalation,  Deupirfenidone, Zinpentraxin alfa, AK 3280, Ianalumab, LTI-03, HZN-825, Tipelukast, ENV-101, PLN-74809, KD025, Setanaxib, TAS-115,Axatilimab, MG-S-2525, GB0139,CSL312 and Saracatinib, others are expected to have a significant impact on the Interstitial Lung Disease market in the coming years.  
  • On March 2024, Boehringer Ingelheim announced a Double Blind, Randomized, Placebo-controlled Trial Evaluating the Efficacy and Safety of BI 1015550 Over at Least 52 Weeks in Patients With Progressive Fibrosing Interstitial Lung Diseases (PF-ILDs).
  • On April 2024, Boehringer Ingelheim announced a Prospective, Observational Study on the Correlations Between Change in Lung Function and Change in Cough and Dyspnoea in Patients With Connective Tissue Disease-associated Progressive Fibrosing INTErstitial luNg diseaSE (CTD Associated PF-ILD) Treated With Nintedanib. The “INTENSE” Study.
  • On January 2024, aTyr Pharma, Inc. announced a Randomized, Double-blind, Placebo-controlled Proof-of-Concept (PoC) Study to Evaluate the Efficacy, Safety, and Tolerability of Efzofitimod in Patients With Systemic Sclerosis (SSc)-Related Interstitial Lung Disease (ILD) (SSc-ILD).

 

Interstitial Lung Disease Overview

Interstitial lung disease (ILD) encompasses a diverse group of disorders characterized by inflammation and scarring of lung tissue, leading to impaired gas exchange. Common symptoms include progressive dyspnea (shortness of breath), cough, and fatigue. ILD can be caused by various factors, including environmental exposures (such as asbestos or silica dust), autoimmune diseases (like rheumatoid arthritis or scleroderma), medications, and genetic predispositions. Diagnosis often involves a combination of clinical evaluation, imaging studies (such as high-resolution CT scans), pulmonary function tests, and sometimes lung biopsies. Treatment aims to alleviate symptoms, slow disease progression, and improve quality of life, and may include medications like corticosteroids, immunosuppressants, or antifibrotic agents. In some cases, lung transplantation may be considered for advanced disease. Prognosis varies depending on the specific type and severity of ILD, with some forms having a better outlook than others. Early detection and management are crucial in optimizing outcomes for patients with ILD.

 

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Interstitial Lung Disease Route of Administration

Interstitial Lung Disease 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
  • Intravenous
  • Subcutaneous

 

Interstitial Lung Disease Molecule Type

Interstitial Lung Disease Products have been categorized under various Molecule types, such as

  • Small molecule
  • Cell Therapy
  • Peptides
  • Polymer
  • Small molecule
  • Gene therapy 

 

Interstitial Lung Disease Pipeline Therapeutics Assessment

  • Interstitial Lung Disease Assessment by Product Type
  • Interstitial Lung Disease By Stage and Product Type
  • Interstitial Lung Disease Assessment by Route of Administration
  • Interstitial Lung Disease By Stage and Route of Administration
  • Interstitial Lung Disease Assessment by Molecule Type
  • Interstitial Lung Disease by Stage and Molecule Type

 

DelveInsight’s Interstitial Lung Disease Report covers around 120+ 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 Interstitial Lung Disease product details are provided in the report. Download the Interstitial Lung Disease pipeline report to learn more about the emerging Interstitial Lung Disease therapies- Interstitial Lung Disease Drugs and Therapies

 

Interstitial Lung Disease Pipeline Analysis:

The Interstitial Lung Disease pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Interstitial Lung Disease 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 Interstitial Lung Disease Treatment.
  • Interstitial Lung Disease key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Interstitial Lung Disease 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 Interstitial Lung Disease market.

 

Download Sample PDF Report to know more about Interstitial Lung Disease drugs and therapies- Interstitial Lung Disease Therapeutics Market

  

Scope of Interstitial Lung Disease Pipeline Drug Insight    

  • Coverage: Global
  • Key Interstitial Lung Disease Companies: AdAlta, Bristol-Myers Squibb, aTyr Pharma, Avalyn Pharmaceuticals, Beijing Continent Pharmaceutical, Regend Therapeutics, Reata Pharmaceuticals, FibroGen, PureTech Health, Bellerophon Pulse Technologies, OncoArendi Therapeutics, LTT Bio-Pharma, EmphyCorp, Genentech, Cudetaxestat, Boehringer Ingelheim, Prometheus Biosciences, HEC Pharm, Bayer, Insmed, Bristol-Myers Squibb, Avalyn Pharma, PureTech Health, Roche, Ark Biosciences, Novartis, Lung Therapeutics, Horizon, MediciNova, Endeavor BioMedicines, Pliant Therapeutics,  Kadmon Pharmaceuticals, GenKyoTex, Taiho Pharmaceutical,Syndax Pharmaceuticals, Metagone Biotech, Galecto Biotech, CSL Behring and AstraZeneca, and others.
  • Key Interstitial Lung Disease Therapies: AD-214, Abatacept, ATYR1923, Pirfenidone inhalation, RO-0220912, Lung stem cells, Bardoxolone methyl, Pamrevlumab, Deupirfenidone, INOpulse, OATD 01, LT 0011, GDC 3280,  Blade Therapeutics, BI 1015550, PRA 023, Yifenidone, Riociguat, Treprostinil Palmitil, BMS 986278, Pirfenidone inhalation,  Deupirfenidone, Zinpentraxin alfa, AK 3280, Ianalumab, LTI-03, HZN-825, Tipelukast, ENV-101, PLN-74809, KD025, Setanaxib, TAS-115,Axatilimab, MG-S-2525, GB0139,CSL312 and Saracatinib, others.
  • Interstitial Lung Disease Therapeutic Assessment: Interstitial Lung Disease current marketed and Interstitial Lung Disease emerging therapies
  • Interstitial Lung Disease Market Dynamics: Interstitial Lung Disease market drivers and Interstitial Lung Disease market barriers 

 

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Table of Contents

1. Interstitial Lung Disease Report Introduction

2. Interstitial Lung Disease Executive Summary

3. Interstitial Lung Disease Overview      

4. Interstitial Lung Disease- Analytical Perspective In-depth Commercial Assessment

5. Interstitial Lung Disease Pipeline Therapeutics

6. Interstitial Lung Disease Late Stage Products (Phase II/III)

7. Interstitial Lung Disease Mid Stage Products (Phase II)

8. Interstitial Lung Disease Early Stage Products (Phase I)

9. Interstitial Lung Disease Preclinical Stage Products

10. Interstitial Lung Disease Therapeutics Assessment

11. Interstitial Lung Disease Inactive Products

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

13. Interstitial Lung Disease Companies

14. Interstitial Lung Disease Key Products

15. Interstitial Lung Disease Unmet Needs

16 . Interstitial Lung Disease Market Drivers and Barriers

17. Interstitial Lung Disease Future Perspectives and Conclusion

18. Interstitial Lung Disease 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.

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Intrahepatic Cholangiocarcinoma Pipeline Analysis 2024: FDA Approvals, Clinical Trials, Therapies, Mechanism of Action, Route of Administration, Companies by DelveInsight

“Intrahepatic Cholangiocarcinoma Pipeline”
Intrahepatic Cholangiocarcinoma companies are TransThera Biosciences, J-Pharma Co., Ltd., Nuvectis Pharma, Inc., Merck, RedHill Biopharma, AnHeart Therapeutics, Tyra Biosciences, Inc., Apollomics and others.

(Albany, United States) As per DelveInsight’s assessment, globally, Intrahepatic Cholangiocarcinoma pipeline constitutes 20+ key companies continuously working towards developing 20+ Intrahepatic Cholangiocarcinoma treatment therapies, analysis of Clinical Trials, Therapies, Mechanism of Action, Route of Administration, and Developments analyzes DelveInsight.

 

“Intrahepatic Cholangiocarcinoma Pipeline Insight, 2024″ report by DelveInsight outlines comprehensive insights into the present clinical development scenario and growth prospects across the Intrahepatic Cholangiocarcinoma Market.

The Intrahepatic Cholangiocarcinoma 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.

 

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Some of the key takeaways from the Intrahepatic Cholangiocarcinoma Pipeline Report:

  • Intrahepatic Cholangiocarcinoma Companies across the globe are diligently working toward developing novel Intrahepatic Cholangiocarcinoma treatment therapies with a considerable amount of success over the years. 
  • Intrahepatic Cholangiocarcinoma companies working in the treatment market are TransThera Biosciences, J-Pharma Co., Ltd., Nuvectis Pharma, Inc., Merck, RedHill Biopharma, AnHeart Therapeutics, Tyra Biosciences, Inc., Apollomics and others, are developing therapies for the Intrahepatic Cholangiocarcinoma treatment 
  • Emerging Intrahepatic Cholangiocarcinoma therapies such as Tinengotinib, Nanvuranlat, NXP 800, and others are expected to have a significant impact on the Intrahepatic Cholangiocarcinoma market in the coming years.
  • In February 2024, Beijing InnoCare Pharma Tech Co., Ltd announced results of a Single-Arm, Open-Label, Multicenter Phase II Study to Evaluate the Efficacy and Safety of ICP-192 in Subjects With Unresectable or Metastatic Intrahepatic Cholangiocarcinoma With FGFR2 Fusions/Rearrangements Who Have Failed Prior Therapy
  • In March 2024, Virogin Biotech Ltd announced results of an Open-Label, Multiple-Center, Phase IIa/IIb Clinical Trial to Evaluate the Efficacy, Safety and Tolerability of VG161 as Monotherapy and in Combination With Nivolumab for Treatment of Patients With Hepatocellular Carcinoma or Intrahepatic Cholangiocarcinoma
  • In November 2021, TransThera announced that the US FDA had granted FTD to its Phase II stage product TT-00420 (tinengotinib) for the treatment of patients with CCA who have no standard treatment options. The grant of FTD is primarily based upon the clinical results of TT-00420 in its completed Phase I study, in which nine CCA patients were enrolled and treated with TT-00420 at different dose levels.

 

Intrahepatic Cholangiocarcinoma Overview

Intrahepatic cholangiocarcinoma (iCCA) is a rare and aggressive form of liver cancer that originates in the bile ducts within the liver. It accounts for approximately 10-20% of all cholangiocarcinoma cases and is often diagnosed at an advanced stage due to its asymptomatic nature in early phases. Risk factors for iCCA include chronic liver disease, bile duct abnormalities, liver fluke infection, and exposure to certain chemicals. Common symptoms, which appear as the disease progresses, include jaundice, abdominal pain, weight loss, and generalized weakness.

Intrahepatic cholangiocarcinoma Diagnosis typically involves imaging techniques such as ultrasound, CT scans, or MRI, complemented by biopsy and blood tests to confirm the presence of cancer cells and assess liver function. Intrahepatic cholangiocarcinoma Treatment options vary depending on the stage of the disease and may include surgical resection, which offers the best chance for a cure if the tumor is localized. For advanced cases, treatment often involves a combination of chemotherapy, radiation therapy, and targeted therapies aimed at specific genetic mutations within the tumor. Despite these treatments, the prognosis for iCCA remains poor, with a high recurrence rate and limited long-term survival. Research is ongoing to better understand the disease and develop more effective therapeutic strategies.

 

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Intrahepatic Cholangiocarcinoma Route of Administration

Intrahepatic Cholangiocarcinoma 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
  • Intravenous
  • Subcutaneous
  • Parenteral
  • Topical

 

Intrahepatic Cholangiocarcinoma Molecule Type

Intrahepatic Cholangiocarcinoma Products have been categorized under various Molecule types, such as

  • Recombinant fusion proteins
  • Small molecule
  • Monoclonal antibody
  • Peptide
  • Polymer
  • Gene therapy

 

Intrahepatic Cholangiocarcinoma Pipeline Therapeutics Assessment

  • Intrahepatic Cholangiocarcinoma Assessment by Product Type
  • Intrahepatic Cholangiocarcinoma By Stage and Product Type
  • Intrahepatic Cholangiocarcinoma Assessment by Route of Administration
  • Intrahepatic Cholangiocarcinoma By Stage and Route of Administration
  • Intrahepatic Cholangiocarcinoma Assessment by Molecule Type
  • Intrahepatic Cholangiocarcinoma by Stage and Molecule Type

 

DelveInsight’s Intrahepatic Cholangiocarcinoma Report covers around 20+ 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 Intrahepatic Cholangiocarcinoma product details are provided in the report. Download the Intrahepatic Cholangiocarcinoma pipeline report to learn more about the emerging Intrahepatic Cholangiocarcinoma therapies- Intrahepatic Cholangiocarcinoma Therapeutics Market

 

Intrahepatic Cholangiocarcinoma Pipeline Analysis:

The Intrahepatic Cholangiocarcinoma pipeline report provides insights into 

  • The report provides detailed insights about companies that are developing therapies for the treatment of Intrahepatic Cholangiocarcinoma 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 Intrahepatic Cholangiocarcinoma Treatment.
  • Intrahepatic Cholangiocarcinoma key companies are involved in targeted therapeutics development with respective active and inactive (dormant or discontinued) projects.
  • Intrahepatic Cholangiocarcinoma 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 Intrahepatic Cholangiocarcinoma market.

 

Download Sample PDF Report to know more about Intrahepatic Cholangiocarcinoma drugs and therapies- Intrahepatic Cholangiocarcinoma Clinical Trials and FDA Approvals

  

Scope of Intrahepatic Cholangiocarcinoma Pipeline Drug Insight    

  • Coverage: Global
  • Key Intrahepatic Cholangiocarcinoma Companies: TransThera Biosciences, J-Pharma Co., Ltd., Nuvectis Pharma, Inc., Merck, RedHill Biopharma, AnHeart Therapeutics, Tyra Biosciences, Inc., Apollomics and others.
  • Key Intrahepatic Cholangiocarcinoma Therapies: Tinengotinib, Nanvuranlat, NXP 800, and others.
  • Intrahepatic Cholangiocarcinoma Therapeutic Assessment: Intrahepatic Cholangiocarcinoma current marketed and Intrahepatic Cholangiocarcinoma emerging therapies
  • Intrahepatic Cholangiocarcinoma Market Dynamics: Intrahepatic Cholangiocarcinoma market drivers and Intrahepatic Cholangiocarcinoma market barriers 

 

Request for Sample PDF Report for Intrahepatic Cholangiocarcinoma Pipeline Assessment and clinical trials – Intrahepatic Cholangiocarcinoma Drugs in Pipeline

 

Table of Contents

1. Intrahepatic Cholangiocarcinoma Report Introduction

2. Intrahepatic Cholangiocarcinoma Executive Summary

3. Intrahepatic Cholangiocarcinoma Overview   

4. Intrahepatic Cholangiocarcinoma- Analytical Perspective In-depth Commercial Assessment

5. Intrahepatic Cholangiocarcinoma Pipeline Therapeutics

6. Intrahepatic Cholangiocarcinoma Late Stage Products (Phase II/III)

7. Intrahepatic Cholangiocarcinoma Mid Stage Products (Phase II)

8. Intrahepatic Cholangiocarcinoma Early Stage Products (Phase I)

9. Intrahepatic Cholangiocarcinoma Preclinical Stage Products

10. Intrahepatic Cholangiocarcinoma Therapeutics Assessment

11. Intrahepatic Cholangiocarcinoma Inactive Products

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

13. Intrahepatic Cholangiocarcinoma Companies

14. Intrahepatic Cholangiocarcinoma Key Products

15. Intrahepatic Cholangiocarcinoma Unmet Needs

16 . Intrahepatic Cholangiocarcinoma Market Drivers and Barriers

17. Intrahepatic Cholangiocarcinoma Future Perspectives and Conclusion

18. Intrahepatic Cholangiocarcinoma 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 Business Research LLP
Contact Person: Ankit Nigam
Email: Send Email
Phone: +14699457679
Address:304 S. Jones Blvd #2432, Las Vegas NV 89107
City: Albany
State: New York
Country: United States
Website: https://www.delveinsight.com/consulting/conference-coverage-services

 

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CBASOX Successfully Renews FinCEN MSB License Strengthening Compliance Operations

CBASOX Exchange has announced the successful renewal of its Money Services Business (MSB) license issued by the Financial Crimes Enforcement Network (FinCEN) of the United States. This renewal extends the license validity until January 9, 2027, following its initial acquisition in 2021.

The initial acquisition of the FinCEN MSB license in 2021 marked the formal entry of CBASOX into the US market, demonstrating compliance with stringent American financial regulations. The successful renewal of this license not only extends the operations of CBASOX in the US but also signifies further recognition from regulatory authorities regarding the operational and compliance frameworks of the platform.

Significance for Users

The renewal of the MSB license signifies a substantial vote of confidence from regulatory authorities in the operational and compliance framework of CBASOX. It sends a clear message to global users that CBASOX is a secure, reliable, and internationally compliant trading platform.

The robust security measures of CBASOX, including excess reserve funds and the use of Merkle tree technology coupled with external audits, further enhance the security and transparency of the platform, providing a safer and more trustworthy trading environment for users.

“We are proud of the successful renewal of our FinCEN MSB license, which validates the long-term commitment of CBASOX to providing secure and compliant trading services,” said Hart Montgomery, a member of the CBASOX team. “Compliance operations and the security of user assets are fundamental to the survival and growth of our platform. We will continue to work closely with global regulatory bodies, constantly improving our service quality and security standards to offer users the best trading experience.”

As a globally recognized cryptocurrency exchange, CBASOX strives to maintain its industry-leading position in technology and service, while also setting benchmarks in compliance and security. Moving forward, CBASOX is committed to fostering the healthy development of the cryptocurrency industry, providing safer and more convenient digital asset trading services to users worldwide.

About CBASOX

CBASOX is a globally leading digital currency trading platform, offering a diverse range of cryptocurrency services including spot trading, options trading, and financial products. Since its establishment, CBASOX has been dedicated to providing a secure, efficient, and convenient trading experience, ensuring platform stability and user asset security through continuous technological innovation and stringent security measures. Through close cooperation with global regulatory bodies, CBASOX has established itself as a responsible and trustworthy exchange in the industry.

Disclaimer: This press release may contain forward-looking statements. Forward-looking statements describe future expectations, plans, results, or strategies (including product offerings, regulatory plans and business plans) and may change without notice. You are cautioned that such statements are subject to a multitude of risks and uncertainties that could cause future circumstances, events, or results to differ materially from those projected in the forward-looking statements, including the risks that actual results may differ materially from those projected in the forward-looking statements.

Media Contact
Company Name: CBASOX DIGITAL TRADE LIMITED
Contact Person: Kim Min-su
Email: Send Email
Country: United States
Website: https://www.cbasox.org

Real Estate Listing Agent in Bozeman, MT, Leverages Local Expertise for Unparalleled Client Satisfaction

Sarah O’Neil, recognized as one of the top real estate listing agents in Bozeman, MT, leverages her extensive local knowledge and unique interior design skills to provide unparalleled client satisfaction in the competitive Bozeman real estate market. With a career that blends deep community roots with professional expertise, Sarah offers an unmatched real estate experience. “My approach is holistic; I combine my local insights with customized staging services to meet the specific needs of each client,” says Sarah, emphasizing the personalized nature of her service.

Sarah’s commitment to her clients is evident in her holistic approach, which encompasses every aspect of buying and selling homes. Her deep understanding of the Bozeman area, paired with her background in real estate and interior design, allows her to provide comprehensive solutions that go beyond typical real estate transactions. “I am dedicated to ensuring that all my clients achieve their real estate goals, whether they are buying or selling,” she explains.

This dedication has driven her to develop exclusive home staging services, which significantly enhance the appeal and functionality of properties on the market. These services not only prepare homes for sale but also help sellers fetch a higher price. “Staging is more than just preparing a house for sale; it’s about creating a vision for potential buyers,” Sarah remarks, highlighting her strategic approach as a Realtor in Bozeman, MT.

Sarah is dedicated to enhancing the appeal of her real estate listings through tailored decluttering and space optimization, even when full staging isn’t required. Specializing in supplemental staging, she skillfully blends clients’ existing furnishings with select art and textiles to elevate property presentations. She emphasizes the crucial role of captivating photography in attracting buyers, especially in today’s market where most homebuyers begin their search online. Her meticulous strategy not only improves virtual showcases but also makes a memorable impact, reflecting a progressive approach to real estate for discerning buyers.

Sarah’s extensive network within the community and her commitment to client satisfaction make her a preferred choice for those looking to navigate the complexities of the real estate market. She understands that each client’s needs are unique and requires tailored strategies to be effectively addressed. “My mission is to ensure that each transaction is as seamless and successful as possible,” she adds.

For anyone looking to buy or sell property in Bozeman, Sarah O’Neil provides the expertise and personal attention needed to succeed. Visit http://www.sarahoneilrealty.com/ to learn more about her services. “Connect with me today, and let’s discuss how I can help you with your real estate needs,” invites Sarah, a committed real estate agent in Bozeman, MT, ready to guide you to success with her extensive local knowledge and proven expertise.

Media Contact
Company Name: Sarah O’Neil Realty | Real Estate Agent in Bozeman MT
Contact Person: Sarah O’Neil
Email: Send Email
Phone: +1 406-579-9836
Address:1001 West Oak St Bldg. C, Suite 111
City: Bozeman
State: Montana 59715
Country: United States
Website: http://www.sarahoneilrealty.com/

 

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