drugset / Trial / NCT03448692

A Study to Evaluate PF-06730512 in Adults With Focal Segmental Glomerulosclerosis (FSGS)

NCT03448692 ↗

Phase 2 Terminated 47 enrolled Pfizer
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

EvaluationDrugModalityDoseRoute
Subject PF-06730512 Protein / enzyme biologic — Intravenous