drugset / Trial / NCT05162066

Study to Evaluate the Safety, Tolerability of BCX9930 in Participants With Either Complement 3 Glomerulopathy (C3G), Immunoglobulin A Nephropathy (IgAN), or Primary Membranous Nephropathy (PMN)

NCT05162066

Phase 2 Terminated 2 enrolled BioCryst Pharmaceuticals
Non-randomizedParallel-groupOpen-labelTreatment

Summary

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

Timeline

Start
2022-02-18
Primary completion
2022-09-23
Completion
2022-09-23

Drugs

EvaluationDrugModalityDoseRoute
Subject BCX9930 Unknown 400 mg Oral