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Clinical Trial Summary

The purpose of the study is to assess PK, Pharmacodynamics (PD), Efficacy and safety of pegcetacoplan in patients with TA-TMA after HSCT.


Clinical Trial Description

This is a pilot study and the sample size is based on practical rather than statistical aspects. A total of 12 patients will be included and treated in the study. With 12 patients included, it is estimated that 9 patients will complete at least 4 weeks of treatment, which is deemed sufficient to characterize the PK of pegcetacoplan in patients with TA-TMA to an appropriate precision. In addition, 12 patients will provide a 72 % probability to observe a response rate of at least 8 responders of the 12 patients recruited (assuming the true response rates is 70 %). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05148299
Study type Interventional
Source Swedish Orphan Biovitrum
Contact Luis Lopez Lazaro, MD
Phone 0041 79 834 17 78
Email Luis.LopezLazaro@sobi.com
Status Recruiting
Phase Phase 2
Start date February 1, 2022
Completion date January 9, 2026