drugset / Trial / NCT02950857

A Study of EPEG in Beta Thalassemia Patients

NCT02950857 ↗

Phase 1 Completed 6 enrolled Prolong Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

An open-label study in which 6 patients will receive once-weekly subcutaneous injections of EPEG for 4 weeks. Final visit will occur 60 days after study entry

Timeline

Start
2017-06-28
Primary completion
2017-09-27
Completion
2017-09-27

Drugs

EvaluationDrugModalityDoseRoute
Subject pegylated erythropoietin Unknown 0.9 ug/kg Subcutaneous
Subject pegylated erythropoietin Unknown 1.2 ug/kg Subcutaneous
Subject pegylated erythropoietin Unknown 1.5 ug/kg Subcutaneous

Indications