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OncoMatch/Clinical Trials/NCT07493135

A Study of IMV102 in Patients With Relapsed/Refractory Multiple Myeloma

Is NCT07493135 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies IMV102 treatment for relapsed/refractory multiple myeloma.

Early Phase 1RecruitingSuzhou Immunofoco Biotechnology Co., LtdNCT07493135Data as of Jun 2026Location: China

Treatment: IMV102 treatmentThis 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.

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Extracted eligibility criteria

Treatments studied

Other

IMV102 treatment

Cancer type

Multiple Myeloma

Performance status

ECOG 0–2(Ambulatory, capable of self-care)

Demographics

Ages ≤ 80

Prior therapy

Min 3 prior lines

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.

Frequently asked questions

Is NCT07493135 currently recruiting?

Yes, this trial is currently recruiting patients.

Is prior treatment required for enrollment?

Yes. Patients must have previously received proteasome inhibitor and immunomodulatory agent.

Is there an age limit?

Yes. Patients must be 80 years or younger.

Could you qualify for this trial?

Enter your biomarker results to see how this trial's eligibility criteria match your specific cancer profile.

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