An Open-label, First-in-human, Single Agent, Dose Escalation Study for the Evaluation of Safety, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of SAR442257 in Patients With Relapsed and Refractory Multiple Myeloma and Relapsed and Refractory Non-Hodgkin Lymphoma
Latest Information Update: 24 Mar 2025
At a glance
- Drugs SAR 442257 (Primary)
- Indications Chronic lymphocytic leukaemia; Cutaneous T-cell lymphoma; Diffuse large B cell lymphoma; Follicular lymphoma; Mantle-cell lymphoma; Marginal zone B-cell lymphoma; Multiple myeloma; Mycosis fungoides; Non-Hodgkin's lymphoma; Sezary syndrome; T-cell lymphoma; Waldenstrom's macroglobulinaemia
- Focus Adverse reactions; First in man
- Sponsors Sanofi
Most Recent Events
- 01 Aug 2024 Planned End Date changed from 14 Aug 2024 to 17 Mar 2025.
- 16 Apr 2024 Planned End Date changed from 24 Apr 2024 to 14 Aug 2024.
- 21 Feb 2024 Planned End Date changed from 15 Apr 2026 to 24 Apr 2024.