A Clinical Study of Gecacitinib Combined With Pegylated Interferon in Patients With PV
NCT07445893 · Status: RECRUITING · Phase: NA · Type: INTERVENTIONAL · Enrollment: 30
Last updated 2026-06-24
Summary
The goal of this clinical trial is to evaluate the efficacy and safety of Gecacitinib in combination with pegylated interferon for the treatment of polycythemia vera (PV).The main question it aims to answer is:
Can PV patients achieve hematological remission after receiving the combination therapy?
Participants will:
Receive combination treatment with Gecacitinib Hydrochloride Tablets and pegylated interferon for 24 weeks Visit the hospital regularly for examinations and follow-up assessments
Conditions
- Polycythemia Vera (PV)
Interventions
- DRUG
-
Gecacitinib Hydrochloride Tablets;Pegylated interferon alfa-2b
Gecacitinib Hydrochloride Tablets: 100 mg twice daily (BID), orally, on an empty stomach. Pegylated interferon alfa-2b: 90 μg once weekly, subcutaneous injection in the abdomen or thigh.
Sponsors & Collaborators
-
Duan Minghui
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
- 2026-04-02
- Primary Completion
- 2026-12-30
- Completion
- 2028-12-30
Countries
- China
Study Locations
More Related Trials
-
Efficacy and Safety of P1101 in Polycythemia Vera Patients for Whom the Standard of Treatment is Difficult to Apply
NCT04182100 ·Status: COMPLETED ·Phase: PHASE2
-
Treatment of Polycythemia Vera With Gleevec
NCT01120821 ·Status: COMPLETED ·Phase: PHASE2
-
A Study to Evaluate P1101 in Japanese PV Patients
NCT06002490 ·Status: COMPLETED ·Phase: PHASE3
-
A Study of IMR-687 in Healthy Adult Volunteers
NCT02998450 ·Status: COMPLETED ·Phase: PHASE1
-
Study on Efficacy and Safety of Givinostat Versus Hydroxyurea in Patients With Polycythemia Vera
NCT06093672 ·Status: RECRUITING ·Phase: PHASE3
-
Long-term Safety and Tolerability of MY008211A Tablets in Patients With Paroxysmal Nocturnal Hemoglobinuria
NCT06933914 ·Status: RECRUITING ·Phase: PHASE2/PHASE3
-
Efficacy and Safety of Ropeginterferon Alfa 2b (P1101) for Patients With Polycythemia Vera
NCT06290765 ·Status: WITHDRAWN ·Phase: PHASE4
-
Safety Evaluation Study for Patients With Polycythemia Vera
NCT05074550 ·Status: UNKNOWN ·Phase: PHASE1
-
A Study to Assess Efficacy, Safety, and Tolerability of P1101 in Adult Patients With PV
NCT05481151 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
Open-Label Study of Oral CEP-701 (Lestaurtinib) in Patients With Polycythemia Vera or Essential Thrombocytosis
NCT00586651 ·Status: COMPLETED ·Phase: PHASE2
-
Phase II Study of GIVINOSTAT (ITF2357) in Combination With Hydroxyurea in Polycythemia Vera
NCT00928707 ·Status: COMPLETED ·Phase: PHASE2
-
Study of Safety and Efficacy of MY008211A in in Patients With Paroxysmal Nocturnal Hemoglobinuria (PNH)
NCT06134414 ·Status: NOT_YET_RECRUITING ·Phase: PHASE2
-
Dasatinib in Polycythemia Vera
NCT00538980 ·Status: TERMINATED ·Phase: PHASE2
-
Transfer of GPI-Linked Proteins to Transfused Patients With Paroxysmal Nocturnal Hemoglobinuria
NCT00039923 ·Status: COMPLETED
-
Study of MGTA-145 and Plerixafor in Patients With Sickle Cell Disease
NCT05445128 ·Status: TERMINATED ·Phase: PHASE2
-
Evaluation of the Safety, Tolerability, Pharmacokinetics (PK) and Effects on Liver Iron Concentration of ICL670 Relative to Deferoxamine(DFO).
NCT01090323 ·Status: COMPLETED ·Phase: PHASE2
-
Efficacy and Safety of Levamisole Combined With Standard Prednisolone in Warm Antibody Autoimmune Hemolytic Anemia.
NCT01579110 ·Status: UNKNOWN ·Phase: PHASE2
-
A Study to Evaluate GBT021601 in Single and Multiple Doses in Healthy Participants
NCT05036512 ·Status: COMPLETED ·Phase: PHASE1
-
Efficacy and Safety of M281 in Adults With Warm Autoimmune Hemolytic Anemia
NCT04119050 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE2/PHASE3
-
Evaluation of Subcutaneous Desferrioxamine as Treatment for Transfusional Hemochromatosis
NCT00000595 ·Status: COMPLETED ·Phase: PHASE2
-
A Phase 1 Study of XL019 in Adults With Polycythemia Vera
NCT00595829 ·Status: TERMINATED ·Phase: PHASE1
-
A Phase 3 Study of Rusfertide in Patients With Polycythemia Vera
NCT05210790 ·Status: ACTIVE_NOT_RECRUITING ·Phase: PHASE3
-
A Study to Evaluate GBT021601-012 Single Dose and Multiple Dose in Participants With Sickle Cell Disease (SCD)
NCT04983264 ·Status: COMPLETED ·Phase: PHASE1
-
Incidence of Iron Deficiency in Polycythemia Vera (PV) and Association With Disease Features
NCT02809274 ·Status: UNKNOWN
-
Iron Balance Study of DFO and GT56-252 in Patients With Transfusional Iron Overload Secondary to Beta-Thalassemia
NCT00069862 ·Status: COMPLETED ·Phase: PHASE1/PHASE2