A Phase I First-in-human, Open-label Trial to Investigate the Safety, Tolerability, Pharmacokinetics and Preliminary Antitumor Activity of SIM0500, A Humanized GPRC5D-BCMA-CD3 Tri-specific Antibody, in Participants With Relapsed or Refractory Multiple Myeloma
Latest Information Update: 29 Jun 2025
At a glance
- Drugs SIM 0500 (Primary)
- Indications Multiple myeloma
- Focus Adverse reactions; First in man
- Sponsors Jiangsu Simcere Pharmaceutical
Most Recent Events
- 18 Jun 2025 Results published in the Media Release
- 18 Jun 2025 According to a Simcere Zaiming media release, Prof. Shaji Kumar looks forward to participating in the Phase 1 study.
- 18 Jun 2025 According to a Simcere Zaiming media release, Dr. Joshua Richter is a Principal investigator of the study.