SIM0500
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
What's the purpose of the trial?
This is an open-label, multicenter phase 1 clinical trial to evaluate the safety and tolerability, efficacy, and pharmacokinetics of SIM0500 in adult participants with Relapsed or Refractory Multiple Myeloma(RRMM).
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Participating Centers
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Experimental Treatments
Learn more about the experimental treatments being evaluated in this clinical trial.
- SIM0500
Arms / Cohorts
Explore eligibility, treatments and learn more about potential cohorts.
Accepting patients
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