drugset / Trial / NCT07653581

rhTPO + CsA vs CsA in the Treatment of LR-MDS With Thrombocytopenia

NCT07653581

Phase 3 Not yet recruiting 78 enrolled Peking Union Medical College Hospital
RandomizedParallel-groupOpen-labelTreatment

Summary

This study aims to compare the efficacy and safety of recombinant human thrombopoietin (rhTPO) + cyclosporine (CsA) and CsA monotherapy in the treatment of lower-risk myelodysplastic neoplasms with thrombocytopenia.

Timeline

Start
2026-06
Primary completion
2028-12
Completion
2029-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide 3 mg/kg
Subject Cyclosporine Peptide 5 mg/kg
Subject recombinant human thrombopoietin Protein / enzyme biologic 300 iu/kg Subcutaneous