drugset / Trial / NCT05350956

A Clinical Study of Herombopag in Tumors-associated Thrombocytopenia

NCT05350956

Non-randomizedSequentialOpen-labelTreatment

Summary

The purpose of this study is to confirm the safety and efficacy of Herombopag in tumors-associated thrombocytopenia

Timeline

Start
2022-06-01
Primary completion
2023-06-01
Completion
2023-10-30

Drugs

EvaluationDrugModalityDoseRoute
Subject RAFUTROMBOPAG Other / unclassified 5 mg Oral
Subject RAFUTROMBOPAG Other / unclassified 7.5 mg Oral
Subject recombinant human thrombopoietin Protein / enzyme biologic 300 iu/kg
Subject recombinant human thrombopoietin Protein / enzyme biologic 15000 iu

Indications