An Open-label, First-in-human, Single Agent, Dose-escalation and Expansion Study for the Evaluation of Safety, Pharmacokinetics, Pharmacodynamics and Anti-tumor Activity of SAR442085 in Patients With Relapsed or Refractory Multiple Myeloma (RRMM)
Latest Information Update: 06 Sep 2024
At a glance
- Drugs SAR 442085 (Primary)
- Indications Multiple myeloma
- Focus Adverse reactions; First in man; Therapeutic Use
- Sponsors Sanofi
- 02 Sep 2024 Status changed from discontinued to completed.
- 19 Sep 2023 Status changed from active, no longer recruiting to discontinued based on sponsor decision (for reasons unrelated to safety, in reviewing Sponsor's evolving portfolio and strategic prioritization).
- 07 Sep 2023 Planned End Date changed from 25 Dec 2023 to 11 Sep 2023.