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Clinical Trial Summary

The study is aimed to evaluate the efficacy of different doses of hetrombopag compared to placebo, measured by the proportion of subjects that can complete two planned consecutive chemotherapy cycles with no modification of chemotherapy regimen (i.e., delayed start, dose reduction, omission, or discontinuation) because of thrombocytopenia [platelet count <100×109/L], to determine an optimal dose of hetrombopag and to demonstrate its superiority over placebo.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05261646
Study type Interventional
Source Jiangsu HengRui Medicine Co., Ltd.
Contact
Status Withdrawn
Phase Phase 3
Start date April 15, 2022
Completion date December 15, 2025

See also
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