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OncoMatch/Clinical Trials/NCT07334119

Safety, Pharmacokinetics, Pharmacodynamics and Preliminary Efficacy of MT-304 in Adults With Advanced HER2-Expressing Solid Tumors

Is NCT07334119 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies multiple treatments including MT-304 and MT-304 + Nivolumab for her2-expressing solid tumors.

Phase 1RecruitingMyeloid TherapeuticsNCT07334119Data as of May 2026

Treatment: MT-304 · MT-304 + NivolumabThis clinical trial is designed to evaluate the safety, pharmacokinetics, pharmacodynamics, and preliminary efficacy of MT-304 in adults with advanced HER2-expressing solid tumors. The main questions it aims to answer are: * What is the safety profile of MT-304 when administered alone or with nivolumab? * What is the recommended Phase 2 dose (RP2D) of MT-304? Participants will: * Receive MT-304 alone (every 14 days) or with nivolumab (every 28 days). * Attend regular clinic visits for assessments and monitoring. * Continue treatment until disease progression, unacceptable toxicity, or study discontinuation.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Biomarker criteria

Required: HER2 (ERBB2) overexpression

Disease stage

Metastatic disease required

metastatic or advanced epithelial cancer expressing HER2

Performance status

ECOG 0–1(Restricted strenuous activity)

Lab requirements

Blood counts

Kidney function

Liver function

Adequate Organ function

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

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