drugset / Trial / NCT04217993

Jaktinib for the Treatment of Ruxolitinib Intolerance of Myelofibrosis

NCT04217993

Phase 2 Completed 51 enrolled Suzhou Zelgen Biopharmaceuticals Co.,Ltd
Non-randomizedParallel-groupOpen-labelTreatment

Summary

This phase IIB, open-label, multicenter study evaluated the efficacy and safety of oral Jaktinib Hydrochloride Tablets in Intermediate-risk and High-risk Myelofibrosis and Previously Treated With Ruxolitinib. The experiment is divided into two parts: dose exploration and extended research.

Timeline

Start
2020-01-07
Primary completion
2022-08-03
Completion
2022-08-03

Drugs

EvaluationDrugModalityDoseRoute
Subject Jaktinib Unknown 100 mg Oral
Subject Jaktinib Unknown 150 mg Oral
Subject Jaktinib Unknown 200 mg Oral