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Clinical Trial Summary

The purpose of this study is to determine the safety and therapeutic potential of BCX9930 in participants with C3G, IgAN, or PMN.


Clinical Trial Description

This is an open-label, multicenter, proof-of-concept study to evaluate the safety, tolerability, and therapeutic potential of BCX9930 administered for 52 weeks in adult (≥ 18 years old) participants with either C3G, IgAN, or PMN. All participants will be enrolled into one of the three parallel treatment cohorts based on diagnosis of C3G, IgAN, or PMN and will receive BCX9930 for the 52-week treatment period. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT05162066
Study type Interventional
Source BioCryst Pharmaceuticals
Contact
Status Terminated
Phase Phase 2
Start date October 29, 2021
Completion date September 23, 2022

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