Brief Description
The purpose of this Phase 2 adaptive study is to evaluate PF-06730512 following multiple intravenous infusions in adult patients with primary FSGS. In addition, the intention is to obtain an early indication of efficacy (how well the drug works at improving Urine Protein to Creatinine Ratio).
Estimated Enrollment
44
Estimated End Date
May, 2023
Trial is for people with
Primary focal segmental glomerulosclerosis (FSGS)
Study Goal
To evaluate the safety, tolerability, and possibly efficacy of PF-06730512 in patients with FSGS.
What is involved for the patient?
Patients will participate for 13 weeks, receiving an intravenous infusion of the study drug weekly.
About the drug or intervention
PF-06730512 works as an antagonist, meaning it possibly reduces the biologic activity that is associated with FSGS.