drugset / Trial / NCT07558434

CsA+EPAG/HPAG+Romiplostim N01 in Newly-diagnosed SAA/TD-NSAA

NCT07558434

Phase 2 Not yet recruiting 43 enrolled Peking Union Medical College Hospital
NaSingle-groupOpen-labelTreatment

Summary

This study aimed to explore the efficacy and safety of cyclosporine (CsA) +eltrombopag (EPAG)/hetrombopag (HPAG)+romiplostim N01 in the treatment of newly-diagnosed transfusion-dependent aplastic anemia (TD-NSAA) and severe aplastic anemia (SAA)

Timeline

Start
2026-04
Primary completion
2028-12
Completion
2029-12

Drugs

EvaluationDrugModalityDoseRoute
Subject Cyclosporine Peptide 3 mg/kg
Subject Cyclosporine Peptide 5 mg/kg
Subject Eltrombopag Small molecule 50 mg
Subject Hetrombopag Small molecule 7.5 mg
Subject Romiplostim N01 Peptide 20 ug/kg Subcutaneous

Indications