OncoMatch/Clinical Trials/NCT07493135
A Study of IMV102 in Patients With Relapsed/Refractory Multiple Myeloma
Is NCT07493135 recruiting? Yes, currently enrolling (May 2026). This Early Phase 1 trial studies IMV102 treatment for relapsed/refractory multiple myeloma.
Treatment: IMV102 treatment — This is an investigator-initiated, single-center, early-phase clinical study comprising dose escalation and dose expansion phases, designed to evaluate the safety and efficacy of IMV102 in subjects with relapsed/refractory multiple myeloma (RRMM). Eligible subjects will receive an infusion of IMV102 injection. Blood and urine samples will be collected before and after infusion for pharmacokinetic, pharmacodynamic, immunogenicity, and safety assessments. Tumor response will be evaluated according to the International Myeloma Working Group (IMWG) uniform response criteria (2016). Assessments will be performed at baseline, and then at Day 28 post-infusion, Month 2, Month 3, and subsequently every 3 months from Month 3 to Month 24, until the subject completes the 24-month follow-up period, experiences disease progression (PD)/relapse, initiates new anti-tumor therapy, dies, or withdraws from the study, whichever occurs first.
Check if I qualifyExtracted eligibility criteria
Cancer type
Multiple Myeloma
Performance status
ECOG 0–2(Ambulatory, capable of self-care)
Prior therapy
Must have received: proteasome inhibitor
including a proteasome inhibitor
Must have received: immunomodulatory agent
immunomodulatory agent-based regimen
Structured fields extracted by AI. May contain errors — verify against the official protocol.
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