Condition: Relapsed/Refractory Multiple Myeloma · Sponsor: Genentech, Inc.
This study will evaluate safety, pharmacokinetics (PK), clinical activity and pharmacodynamics (PD) of RO7851624 in participants with RRMM who are triple-class exposed (treated with proteasome inhibitors \[PIs\], immunomodulators \[IMiDs\], and anti-cluster of differentiation 38 \[anti-CD38\] monoclonal antibodies), and have limited remaining standard treatment options due to refractoriness, intolerance, or multiple prior therapies.
This description comes directly from the study's public registry record.
Reference Study ID Number: GO46140 https://forpatients.roche.com/ No attachments to email below. · 888-662-6728 (U.S. and Canada) · global-roche-genentech-trials@gene.com
Fastest response: use the inquiry form. https://www.gene.com/contact-us/submit-medical-inquiry
Always discuss trial participation with your own doctor first.
| Peter MacCallum Cancer Center | Parkville, Victoria, Australia | Recruiting |
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Source record: clinicaltrials.gov/study/NCT07558915