Trial Search Results
A Study of Fresolimumab in Patients With Steroid-Resistant Primary Focal Segmental Glomerulosclerosis (FSGS)
The primary objectives of this trial are as follows:
- to compare the achievement of a partial remission (PR) or complete remission (CR) in urinary protein: creatinine ratio (Up/c ratio) in patients treated with fresolimumab versus placebo
- to compare the safety profile of patients treated with fresolimumab versus placebo
The secondary objectives are as follows:
- To compare the reduction in proteinuria in patients treated with fresolimumab versus placebo
- To evaluate fresolimumab dose-dependent reduction in proteinuria
- To compare the change in renal function (estimated glomerular filtration rate [eGFR]) in patients treated with fresolimumab versus placebo
- To evaluate the multiple-dose pharmacokinetics of fresolimumab
Stanford is currently not accepting patients for this trial.
Genzyme, a Sanofi Company
- Drug: fresolimumab
- Drug: fresolimumab
- Drug: Placebo
- The patient's renal biopsy is consistent with the diagnosis of primary Focal Segmental
Glomerulosclerosis (FSGS) including all histological subtypes.
- The patient has an eGFR ≥ 30 mL/min/1.73 m2
- The patient has a urinary total protein:creatinine ratio ≥ 3 mg protein/mg creatinine
- In the opinion of the Investigator, the patient has steroid-resistant FSGS. The
patient must have been treated for FSGS with a course of high-dose steroid therapy for
a minimum of 4 weeks
- The patient has been treated with an ACEi (angiotensin converting enzyme inhibitor)
and/or ARB (angiotensin receptor blocker) at a stable dose for a minimum of 4 weeks
prior to Visit 2 (treatment start)
- The patient has FSGS which in the Investigator's opinion is secondary to another
- The patient has been taking prednisone at a dose > 10 mg/day (or equivalent dose of an
alternative glucocorticoid) within 4 weeks prior to Visit 1 (Screening Visit).
- The patient has received any other systemically administered immunosuppressive drugs
(other than glucocorticoids) within 8 weeks prior to Visit 1.
- The patient has received rituximab within 6 months prior to Visit 1.
- The patient has a history of organ transplantation.
Ages Eligible for Study
18 Years - N/A
Genders Eligible for Study