drugset / Trial / NCT03448692
A Study to Evaluate PF-06730512 in Adults With Focal Segmental Glomerulosclerosis (FSGS)
Non-randomizedSequentialTriple-blindTreatment
Summary
The purpose of this Phase 2 adaptive study is to evaluate the efficacy, safety, tolerability and pharmacokinetics of PF-06730512 following multiple intravenous infusions in adult subjects with FSGS.
Timeline
- Start
- 2018-10-15
- Primary completion
- 2023-02-14
- Completion
- 2023-02-14
Outcome
Outcome not reported
Stopped: “The study was terminated due to lack of efficacy at both tested doses on 5th December 2022. The decision to terminate the study is not related to a safety concern.”
Drugs
| Evaluation | Drug | Modality | Dose | Route |
|---|---|---|---|---|
| Subject | PF-06730512 | Protein / enzyme biologic | — | Intravenous |