Ropeginterferon for High Risk JAK2 Clonal Hematopoiesis
NCT07249840 · Status: NOT_YET_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 12
Last updated 2025-11-25
Summary
The goal of this clinical trial is to learn if the drug ropeginterferon alfa-2b can be used safely to treat patients with a JAK2 mutation and high risk features, but do not yet have a myeloproliferative neoplasm. The main questions it aims to answer are:
* Can we enroll 12 patients with JAK2 mutations and high risk features without a myeloproliferative neoplasm on a clinical trial evaluating the drug ropeginterferon?
* Is ropeginterferon safe to use in these patients?
Participants will:
* Receive ropeginterferon as an injection under the skin once every 4 weeks
* Visit the clinic every 1-3 months for checkups and tests
Conditions
- JAK2 Mutation
Interventions
- DRUG
-
Ropeginterferon
Patients will receive Ropeginterferon
Sponsors & Collaborators
-
Brigham and Women's Hospital
lead OTHER
Study Design
- Allocation
- NA
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2026-06-30
- Primary Completion
- 2030-06-30
- Completion
- 2030-06-30
- FDA Drug
- Yes
Countries
- United States
Study Locations
More Related Trials
-
Pacritinib w/ Talazoparib in Pts w/ Myeloproliferative Neoplasms Unresponsive to JAK2 Inhibition
NCT06218628 ·Status: RECRUITING ·Phase: PHASE1
-
A Study of LNK01002 in Patients With Primary or Secondary Myelofibrosis,Polycythemia Vera or Acute Myeloid Leukemia
NCT04896112 ·Status: WITHDRAWN ·Phase: PHASE1
-
Study of TL-895 Combined With Ruxolitinib in JAKi Treatment-Naïve MF Subjects and Subjects With MF Who Have a Suboptimal Response to Ruxolitinib
NCT05280509 ·Status: RECRUITING ·Phase: PHASE1/PHASE2
-
Study of the JAK Inhibitor Ruxolitinib Administered Orally to Patients With Primary Myelofibrosis (PMF), Post-Polycythemia Vera-Myelofibrosis (PPV-MF) or Post-Essential Thrombocythemia-Myelofibrosis (PET-MF)
NCT01317875 ·Status: COMPLETED ·Phase: PHASE1
-
Panobinostat and Ruxolitinib in Primary Myelofibrosis, Post-polycythemia Vera-myelofibrosis or Post-essential Thrombocythemia-myelofibrosis
NCT01433445 ·Status: COMPLETED ·Phase: PHASE1
-
Long-Term Side Effects of Ruxolitinib in Treating Patients With Myelofibrosis
NCT02784496 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Combination Ruxolitinib and Decitabine Treatment for Accelerated Phase MPN or Post-MPN AML
NCT02076191 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
Phase II Study Assessing the Safety and Efficacy of Dasatinib in Combination With Ropeginterferon in Patients With Newly Diagnosed Chronic Myeloid Leukemia in Chronic Phase
NCT07269470 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
A Study to Evaluate INCA035784 in Participants With Myeloproliferative Neoplasms
NCT07008118 ·Status: RECRUITING ·Phase: PHASE1
-
CINC424A2X01B Rollover Protocol
NCT02386800 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE4
-
Evaluation of the Pathobiology of CALR-mutated MPN Cells
NCT06480591 ·Status: RECRUITING
-
A Study in Myeloproliferative Disorders
NCT01134120 ·Status: COMPLETED ·Phase: PHASE1
-
Testing the Effect of Taking Ruxolitinib and CPX-351 in Combination for the Treatment of Advanced Phase Myeloproliferative Neoplasms
NCT03878199 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
A Study to Find the Maximum Tolerated Dose of the Experimental Combination of the Drugs INC424 and BKM120 in Patients With Primary or Secondary Myelofibrosis
NCT01730248 ·Status: TERMINATED ·Phase: PHASE1
-
Phase III Study Investigating the Efficacy and Safety of Ruxolitinib in Early Myelofibrosis Patients With High Molecular Risk Mutations.
NCT02598297 ·Status: TERMINATED ·Phase: PHASE3
-
Mutant CALR-peptide Based Vaccine in Patients With Mutated CALR Myeloproliferative Neoplasm
NCT05025488 ·Status: RECRUITING ·Phase: PHASE1
-
A Long-Term Study of the Effects of Orally Administered SAR302503 in Patients With Myelofibrosis
NCT00724334 ·Status: COMPLETED ·Phase: PHASE1/PHASE2
-
INCB000928 Administered as a Monotherapy or in Combination With Ruxolitinib in Participants With Anemia Due to Myeloproliferative Disorders
NCT04455841 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE1/PHASE2
-
Phase l/II Study of Ruxolitinib for Acute Leukemia
NCT01251965 ·Status: TERMINATED ·Phase: PHASE1/PHASE2
-
Phase 2 Study of SAR302503 in Patients With Myelofibrosis
NCT01420770 ·Status: COMPLETED ·Phase: PHASE2
-
A Clinical Study to Test the Effects of Ruxolitinib And Thalidomide Combination for Patients With Myelofibrosis
NCT03069326 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2
-
A Phase 2 Study of Ruxolitinib With Chemotherapy in Children With Acute Lymphoblastic Leukemia
NCT02723994 ·Status: COMPLETED ·Phase: PHASE2
-
Asian Phase II Study of INC424 in Patients With Primary Myelofibrosis (MF), Post-PV MF or Post-ET MF
NCT01392443 ·Status: COMPLETED ·Phase: PHASE2
-
Momelotinib Versus Ruxolitinib in Subjects With Myelofibrosis
NCT01969838 ·Status: COMPLETED ·Phase: PHASE3
-
Ruxolitinib for Patients With Low or Intermediate-1 Risk Myelodysplastic Syndrome (MDS)
NCT01895842 ·Status: COMPLETED ·Phase: PHASE1