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OncoMatch/Clinical Trials/NCT07294625

A Clinical Study to Evaluate LVIVO-TaVec200 for the Treatment of Relapsed/Refractory Multiple Myeloma

Is NCT07294625 recruiting? Yes, currently enrolling (Jun 2026). This Early Phase 1 trial studies LVIVO-TaVec200 product for multiple myeloma.

Early Phase 1RecruitingThe First Affiliated Hospital with Nanjing Medical UniversityNCT07294625Data as of Jun 2026Location: China

Treatment: LVIVO-TaVec200 productThis is a prospective, single-arm, open-label dose-escalation clinical study to evaluate LVIVO-TaVec200 in the treatment of relapsed/refractory multiple myeloma.

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Extracted eligibility criteria

Treatments studied

Other

LVIVO-TaVec200 product

Cancer type

Multiple Myeloma

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Cannot have received: antitumor therapy

Exception: insufficient washout period

Prior antitumor therapy with insufficient washout period

Cannot have received: GPRC5D-targeted therapy

Prior treatment targeting GPRC5D

Structured fields extracted by AI. May contain errors — verify against the official protocol.

Frequently asked questions

Is NCT07294625 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior antitumor therapy, GPRC5D-targeted therapy disqualifies patients from enrollment.

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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