GR1803 Injection in Patients With RRMM

Summary

All subjects will receive GR1803 injection until intolerable toxicity or investigator-assessed disease progression occurs (except in cases of disease progression due to discontinuation of the drug as a result of an adverse event) or until the subject has been administered the drug for 2 years or until the subject withdraws consent or until the investigator determines that the subject needs to be discontinued.

Timeline

Start

2025-04-24

Primary completion

2027-07-01

Completion

2027-12-01

Drugs

Indications