Primary Objectives: * Dose Escalation Part A: To determine the maximum tolerated dose (MTD) of SAR442085 administered as a single agent in patients with relapsed or refractory multiple myeloma (RRMM), and determine the recommended Phase 2 dose (RP2D) for the subsequent Expansion Part B * Dose Expansion Part B: To assess the antitumor activity of single agent of SAR442085 at the RP2D in patients with RRMM Secondary Objectives: * To characterize the safety profile of SAR442085 * To characterize the pharmacokinetics (PK) profile of SAR442085 when administered as a single agent * To evaluate the potential immunogenicity of SAR442085 * To assess preliminary evidence of antitumor activity in the Dose Escalation Part A
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AI-rewrites the medical criteria so a patient or caregiver can understand them. Always confirm with the trial site.
The maximum tolerated dose (MTD) of SAR442085 (Part A)
Timeframe: At the end of Cycle 1 (each cycle is approximately 28 days)
Recommended Phase 2 dose (RP2D) (Part A)
Timeframe: At the end of Cycle 1 (each cycle is approximately 28 days)
Overall response rate (Part B)
Timeframe: approximately 6 months after the last patient has started treatment in Part B (approx. 2 years)