drugset / Trial / NCT03222843

Multicentre, Randomised Phase III Study of the Efficacy and Safety of Hetrombopag Olamine in Idiopathic Thrombocytopenic Purpura (ITP) Patient

NCT03222843 ↗

Phase 3 Completed 424 enrolled Jiangsu HengRui Medicine Co., Ltd.
RandomizedParallel-groupQuadruple-blindTreatment

Summary

A multicentre, randomised, double-blind,4-stages phase III study enrolled 414 patients with chronic, previously treated ITP. Dosage could be adjusted (2.5\~.75 mg/day) to maintain platelet counts 50\~250×109/L

Timeline

Start
2017-06-30
Primary completion
2019-11-11
Completion
2021-01-07

Outcome

Met primary endpoint

paper The primary endpoint was achieved by significantly more patients in the HETROM-2.5 (58.9%; odds ratio [OR] 25.97, 95% confidence interval [CI] 9.83-68.63; p < 0.0001) PMID 33632264 ↗

paper and HETROM-5 (64.3%; OR 32.81, 95% CI 12.39-86.87; p < 0.0001) group than in the Placebo group (5.9%). PMID 33632264 ↗

Drugs

EvaluationDrugModalityDoseRoute
Subject Hetrombopag Small molecule 2.5 mg Oral
Subject Hetrombopag Small molecule 5 mg Oral