Overview
Primary Objectives:
- Phase 1: To characterize the safety and tolerability of isatuximab in kidney transplant candidates.
- Phase 2: To evaluate the efficacy of isatuximab in desensitization of patients awaiting kidney transplantation.
Secondary Objectives:
- Phase 2: To characterize the safety profile of isatuximab in kidney transplant candidates.
- To characterize the pharmacokinetic (PK) profile of isatuximab in kidney transplant candidates.
- To evaluate the immunogenicity of isatuximab.
- To assess the overall efficacy of isatuximab in desensitization of patients awaiting kidney transplantation.
Description
The study will have a screening period of up to 28 days, a treatment period of up to 12 weeks, a site visit FUP of up to 26 weeks, and an extended FUP until study cutoff.
The study duration that involves site visit per participant (ie, screening, treatment, site visit FUP) will be approximately 42 weeks.
The study duration including extended FUP per participant will be approximately 78 weeks (depending when the participant is enrolled).
Eligibility
Inclusion criteria :
- Diagnosis of chronic kidney disease (CKD) and active candidate on the kidney donor waitlist at the time of screening.
- Body mass index (BMI) 40 kg/m2.
- Contraceptive use by men or women should be consistent with local regulations regarding the methods of contraception for those participating in clinical studies.
- Capable of giving signed informed consent.
For Participants in Cohort A: active candidates on the kidney waitlist with living donor.
For participants in Cohort B: active candidates on the kidney waitlist with no living donor cleared for donation.
Exclusion criteria:
- Significant cardiac dysfunction
- Known active, recurrent, or chronic infection
- Active lupus or uncontrolled diabetes
- Prior treatment with rituximab within 6 months from SAR650984 administration
- Inadequate organ and bone marrow function at screening
- Pregnant or breastfeeding women or women who intend to become pregnant during participation in the study
- Known intolerance or hypersensitivity to any component of SAR650984 or premedications
- Participants who are not suitable for participation as judged by the Investigator
The above information is not intended to contain all considerations relevant to a patient's potential participation in a clinical trial.