drugset / Trial / NCT06433830

Hetrombopag for the Thrombocytopenia Induced by Concurrent Chemoradiotherapy

NCT06433830

Phase 2 Unknown 50 enrolled Sir Run Run Shaw Hospital
NaSingle-groupOpen-labelSupportive care

Summary

Thrombocytopenia represents one of the main toxicities of concurrent chemoradiotherapy, which may necessitate chemotherapy dose reductions, dose delays, or discontinuation, and even compromise survival. Hetrombopag, a thrombopoietin receptor agonist, has shown efficacy and safety in patients with chemotherapy-induced thrombocytopenia. However, the efficacy of hetrombopag in patients who received concurrent chemoradiotherapy is not clear yet. This study aimed to evaluate the efficacy and safety of hetrombopag in this patient population.

Timeline

Start
2022-05-10
Primary completion
2025-05-30
Completion
2025-07-30

Drugs

EvaluationDrugModalityDoseRoute
Subject Hetrombopag Small molecule 7.5 mg Oral

Indications