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OncoMatch/Clinical Trials/NCT07317505

A Phase 1 Study of JMT108 in Participants With Advanced Solid Tumors

Is NCT07317505 recruiting? Yes, currently enrolling (Jun 2026). This Phase 1 trial studies JMT108 for cancer.

Phase 1RecruitingConjupro Biotherapeutics, Inc.NCT07317505Data as of Jun 2026

Treatment: JMT108The goal of this clinical trial is to test JMT108, a type of drug called a bispecific antibody in adult patients with locally advanced or metastatic solid tumors. The main questions it aims to answer are: * To assess the safety and tolerability of JMT108 at increasing doses and determine the dose and schedule to be used in the second part of the study (Phase 1a) * To assess effectiveness of JMT108 in participants with locally advanced or metastatic tumors (Phase 1b) * To evaluate how quickly JMT108 is metabolized by the body (pharmacokinetics or PK) * To evaluate if antibodies to the study drug develop (immunogenicity) * To evaluate preliminary efficacy to the drug * To explore the pharmacodynamic (PD) characteristics of JMT108 * To explore the correlation between biomarker levels and preliminary efficacy Participants will: * Provide written informed consent * Undergo screening tests to ensure they are eligible for study treatment * Attend all required study visits and receive JMT108 by intravenous injection every 2 weeks until the study doctor determines study treatment should be stopped, based on how well a participant is doing on treatment * Be followed for progression every 3 months for up to 2 years

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Extracted eligibility criteria

Treatments studied

Other

JMT108

Cancer type

Tumor Agnostic

Performance status

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

Prior therapy

Must have received: standard of care

Participants...who are unresponsive or intolerant to all standard of care or have no standard of care available

Cannot have received: unapproved investigational drugs or treatments

Any other unapproved investigational drugs or treatments within 4 weeks prior to the first dose of the investigational drug (C1D1)

Cannot have received: chemotherapy

Exception: nitrosoureas or mitomycin C within 6 weeks

Chemotherapy...within 4 weeks prior to the first dose of the investigational drug, except in the following situations: 1. Nitrosoureas or mitomycin C within 6 weeks prior to the first dose

Cannot have received: radiotherapy

Radiotherapy within 4 weeks prior to the first dose of the investigational drug

Cannot have received: biological therapy

Biological therapy within 4 weeks prior to the first dose of the investigational drug

Cannot have received: endocrine therapy

Endocrine therapy within 4 weeks prior to the first dose of the investigational drug

Cannot have received: targeted therapy

Exception: oral fluoropyrimidines and small-molecule targeted drugs within 2 weeks or 5 half-lives (whichever is longer)

Targeted therapy within 4 weeks prior to the first dose of the investigational drug, except in the following situations: 2. Use of oral fluoropyrimidines and small-molecule targeted drugs within 2 weeks or 5 half-lives of the drug (whichever is longer)

Cannot have received: immunotherapy

Immunotherapy within 4 weeks prior to the first dose of the investigational drug

Cannot have received: other anti-tumor therapies

Exception: herbal medicine/products with anti-tumor indications within 2 weeks

Other anti-tumor therapies within 4 weeks prior to the first dose of the investigational drug, except in the following situations: 3. Use of herbal medicine/products with anti-tumor indications within 2 weeks prior to the first dose

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

US trial sites

  • Carolina BioOncology Institute · Huntersville, North Carolina
  • NEXT Dallas · Dallas, Texas
  • NEXT Virginia · Fairfax, Virginia

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07317505 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior unapproved investigational drugs or treatments, chemotherapy, radiotherapy 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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