Press release
Post-Polycythemia Vera Myelofibrosis Clinical Trials 2025: EMA, PDMA, FDA Approvals, Medication, Treatment Market, NDA Approval, Therapies, ROA, MOA and Companies by DelveInsight | Kartos Therapeutics, Inc., Parexel, Constellation Pharmaceuticals, Incyte
Post-Polycythemia Vera Myelofibrosis Clinical Trials
According to DelveInsight, the Post-Polycythemia Vera Myelofibrosis pipeline comprises 17+ pharmaceutical and biotech companies actively developing 17+ therapeutic candidates targeting Post-Polycythemia Vera Myelofibrosis. These therapies span various stages of clinical and non-clinical development, underscoring the intense innovation and commitment to addressing one of the most pressing public health challenges of our time.
With Post-Polycythemia Vera Myelofibrosis reaching epidemic proportions globally and contributing significantly to comorbid conditions such as diabetes, cardiovascular disease, and certain cancers, there is a growing demand for safer, more effective treatment options.
Explore the Cutting-Edge Landscape of Post-Polycythemia Vera Myelofibrosis Drug Development @ https://www.delveinsight.com/report-store/post-polycythemia-vera-myelofibrosis-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=apr
Key Takeaways from the Post-Polycythemia Vera Myelofibrosis Pipeline Report
• DelveInsight's Post-Polycythemia Vera Myelofibrosis pipeline report depicts a robust space with 17+ active players working to develop 17+ pipeline therapies for Post-Polycythemia Vera Myelofibrosis treatment.
• In July 2025, Celgene has announced a Phase 3, Multicenter, Open-label, Randomized Study to Evaluate the Efficacy and Safety of Fedratinib Compared to Best Available Therapy (BAT) in Subjects With DIPSS (Dynamic International Prognostic Scoring System)-Intermediate or High-risk Primary Myelofibrosis (PMF), Post-polycythemia Vera Myelofibrosis (Post-PV MF), or Post-essential Thrombocythemia Myelofibrosis (Post-ET MF) and Previously Treated With Ruxolitinib
• In July 2025, Incyte Corporation has announced results of a Phase 1/2 Open-Label, Multicenter Study of INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders
• In June 2025, Swedish Orphan Biovitrum has announced results of a Randomized, Controlled Phase 3 Study of Pacritinib Versus Physician's Choice in Patients With Primary Myelofibrosis, Post Polycythemia Vera Myelofibrosis, or Post-Essential Thrombocythemia Myelofibrosis With Severe Thrombocytopenia.
• In September 2023, the FDA approved momelotinib for the treatment of adults with intermediate- or high-risk myelofibrosis, including PPV-MF, who have anemia. Momelotinib is a once-daily oral inhibitor of JAK1, JAK2, and activin A receptor type 1 (ACVR1). It is the first therapy approved that addresses anemia, constitutional symptoms, and splenomegaly in myelofibrosis patients.
• Key Post-Polycythemia Vera Myelofibrosis companies such as Kartos Therapeutics, Inc., Parexel, Constellation Pharmaceuticals, Incyte Corporation, NS Pharma, Celgene, Lynk Pharmaceuticals Co., Ltd, Imago BioSciences, Inc., Karyopharm Therapeutics Inc, and others are evaluating new drugs for Post-Polycythemia Vera Myelofibrosis to improve the treatment landscape.
• Promising Post-Polycythemia Vera Myelofibrosis pipeline therapies in various stages of development include Navtemadlin, Selinexor, and others.
Post-Polycythemia Vera Myelofibrosis Overview:
When Polycythemia Vera progresses into myelofibrosis, it is known as post-polycythemia vera myelofibrosis (PPV-MF). Myelofibrosis (MF) is a rare, chronic form of blood cancer characterized by a malfunction in the bone marrow that leads to abnormal blood cell production and the development of fibrous scar tissue.
Interestingly, PPV-MF is now recognized as one of the most frequently diagnosed types of intracranial tumors in the United States, with an estimated 98,000 to 170,000 new cases reported annually. Several factors have contributed to this rising incidence. Advances in systemic therapies-especially immunotherapies-have extended the survival of patients with widespread metastatic disease, giving more time for secondary complications like PPV-MF to develop. Additionally, improvements in magnetic resonance imaging (MRI) technology have enhanced the ability to detect small, asymptomatic cases, contributing to more frequent diagnoses.
Download the Post-Polycythemia Vera Myelofibrosis sample report to know in detail about the Post-Polycythemia Vera Myelofibrosis treatment market @ https://www.delveinsight.com/sample-request/post-polycythemia-vera-myelofibrosis-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=apr
Post-Polycythemia Vera Myelofibrosis Pipeline Analysis
The Post-Polycythemia Vera Myelofibrosis pipeline insights report 2025, provides insights into:
• Provides comprehensive insights into key companies developing therapies in the Post-Polycythemia Vera Myelofibrosis Market.
• Categorizes Post-Polycythemia Vera Myelofibrosis therapeutic companies by development stage: early, mid, and late-stage.
• Highlights major companies involved in targeted therapy development, including both active and inactive (paused/discontinued) projects.
Reviews emerging Post-Polycythemia Vera Myelofibrosis drugs under development based on:
• Stage of development
• Post-Polycythemia Vera Myelofibrosis Route of administration
• Target receptor
• Monotherapy vs. combination therapy
• Post-Polycythemia Vera Myelofibrosis Mechanism of action
• Molecular type
Offers detailed analysis of:
• Company-to-company and company-academia collaborations
• Post-Polycythemia Vera Myelofibrosis Licensing agreements
• Funding and investment activities supporting future Post-Polycythemia Vera Myelofibrosis market advancement.
Unlock key insights into emerging Post-Polycythemia Vera Myelofibrosis therapies and market strategies here: https://www.delveinsight.com/report-store/post-polycythemia-vera-myelofibrosis-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=apr
Post-Polycythemia Vera Myelofibrosis Emerging Drugs
Navtemadlin - Kartos Therapeutics, Inc.
Navtemadlin (KRT-232) is an investigational cancer therapy that specifically targets and inhibits the MDM2 protein. Preclinical studies, including cell cultures and cancer models, have shown that navtemadlin effectively blocks MDM2 at low concentrations, triggering a dose-dependent activation of the p53 pathway. This activation leads to cell cycle arrest via p21 and promotes cell death through pro-apoptotic Bcl-2 family proteins, resulting in complete and sustained tumor regression. Promising clinical responses have been observed in patients with various advanced cancers such as myelofibrosis, acute myeloid leukemia, and Merkel cell carcinoma. The therapy is currently in Phase II/III trials for treating Post-Polycythemia Vera Myelofibrosis (Post-PV-MF).
Selinexor - Karyopharm Therapeutics Inc.
Selinexor is an innovative, orally administered drug that belongs to a class called Selective Inhibitors of Nuclear Export (SINE). It works by binding to and blocking the function of XPO1, a nuclear export protein. This inhibition causes tumor suppressor proteins to accumulate in the cell nucleus, restoring and enhancing their ability to suppress tumor growth. The process selectively triggers cancer cell death while sparing most normal cells. Selinexor is currently being evaluated in a Phase II clinical trial to assess its safety and effectiveness in patients with myelofibrosis-including primary (PMF), post-essential thrombocythemia (PET-MF), and post-polycythemia vera (PPV-MF) types-who are resistant or intolerant to JAK1/2 inhibitors.
Post-Polycythemia Vera Myelofibrosis Pipeline Therapeutic Assessment
Post-Polycythemia Vera Myelofibrosis Assessment by Product Type
• Mono
• Combination
• Mono/Combination
Post-Polycythemia Vera Myelofibrosis By Stage
• Late-stage products (Phase III)
• Mid-stage products (Phase II)
• Early-stage product (Phase I) along with the details of
• Pre-clinical and Discovery stage candidates
• Discontinued & Inactive candidates
Post-Polycythemia Vera Myelofibrosis Assessment by Route of Administration
• Oral
• Parenteral
• Intravenous
• Subcutaneous
• Topical
Post-Polycythemia Vera Myelofibrosis Assessment by Molecule Type
• Recombinant fusion proteins
• Small molecule
• Monoclonal antibody
• Peptide
• Polymer
• Gene therapy
Download sample pages to get an in-depth assessment of the emerging Post-Polycythemia Vera Myelofibrosis therapies and key Post-Polycythemia Vera Myelofibrosis companies: https://www.delveinsight.com/sample-request/post-polycythemia-vera-myelofibrosis-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=apr
Table of Contents
1. Report Introduction
2. Executive Summary
3. Post-Polycythemia Vera Myelofibrosis Current Treatment Patterns
4. Post-Polycythemia Vera Myelofibrosis - DelveInsight's Analytical Perspective
5. Therapeutic Assessment
6. Post-Polycythemia Vera Myelofibrosis Late-Stage Products (Phase-III)
7. Post-Polycythemia Vera Myelofibrosis Mid-Stage Products (Phase-II)
8. Early Stage Products (Phase-I)
9. Pre-clinical Products and Discovery Stage Products
10. Inactive Products
11. Dormant Products
12. Post-Polycythemia Vera Myelofibrosis Discontinued Products
13. Post-Polycythemia Vera Myelofibrosis Product Profiles
14. Post-Polycythemia Vera Myelofibrosis Key Companies
15. Post-Polycythemia Vera Myelofibrosis Key Products
16. Dormant and Discontinued Products
17. Post-Polycythemia Vera Myelofibrosis Unmet Needs
18. Post-Polycythemia Vera Myelofibrosis Future Perspectives
19. Post-Polycythemia Vera Myelofibrosis Analyst Review
20. Appendix
21. Report Methodology
Request the sample PDF to get detailed insights about the Post-Polycythemia Vera Myelofibrosis pipeline reports offerings: https://www.delveinsight.com/report-store/post-polycythemia-vera-myelofibrosis-pipeline-insight?utm_source=openpr&utm_medium=pressrelease&utm_campaign=apr
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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.
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