Safety and Efficacy of Romiplostim in Treatment of Chronic ITP in Children

Not yet recruitingOBSERVATIONAL
Enrollment

100

Participants

Timeline

Start Date

November 1, 2025

Primary Completion Date

November 1, 2026

Study Completion Date

January 1, 2027

Conditions
Romiplostim N01ITP
Interventions
DRUG

Safety and efficacy of Romiplostim in Treatment of chronic ITP in children

Children diagnosed with chronic immune thrombocytopenia (ITP) will receive Romiplostim, a thrombopoietin receptor agonist administered as a once-weekly subcutaneous injection. The initial dose will be 1 µg/kg, with subsequent dose adjustments (up to a maximum of 10 µg/kg weekly) based on platelet response, in order to maintain platelet counts ≥50 × 10⁹/L while minimizing the risk of bleeding. Treatment duration will be determined according to study protocol, and patients will be monitored regularly for efficacy (platelet count response, bleeding events) and safety (adverse events, laboratory parameters).

All Listed Sponsors
lead

Assiut University

OTHER

NCT07214025 - Safety and Efficacy of Romiplostim in Treatment of Chronic ITP in Children | Biotech Hunter | Biotech Hunter