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OncoMatch/Clinical Trials/NCT07046923

A Study of LY4175408 in Participants With Advanced Cancer

Is NCT07046923 recruiting? Yes, currently enrolling (Sep 2026). This Phase 1 trial studies multiple treatments including LY4175408 and Pembrolizumab for carcinoma, non-small-cell lung.

Phase 1RecruitingEli Lilly and CompanyNCT07046923Data as of Sep 2026Location: International · 6 countries

Treatment: LY4175408 · Pembrolizumab · Carboplatin · CisplatinThe purpose of this study is to measure the safety and efficacy of LY4175408 in participants with selected advanced cancer. In addition, this study will evaluate how much LY4175408 gets into the bloodstream, how it is broken down, and how long it takes the body to get rid of it. Participation could last up to 4 years.

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Extracted eligibility criteria

Treatments studied

Immunotherapy

Pembrolizumab

Chemotherapy

CarboplatinCisplatin

Other

LY4175408

Cancer type

Non-Small Cell Lung Carcinoma

Small Cell Lung Cancer

Endometrial Cancer

Triple-Negative Breast Cancer

Breast Carcinoma

Biomarker criteria

Required: EGFR wild-type

NSCLC with no known actionable genomic alterations

Required: ALK wild-type

NSCLC with no known actionable genomic alterations

Required: ROS1 wild-type

NSCLC with no known actionable genomic alterations

Performance status

ECOG 0–1(Restricted strenuous activity)

Prior therapy

Max 2 prior lines

Cannot have received: protein tyrosine kinase 7 antibody-drug conjugate with topoisomerase I inhibitor payload

Prior treatment with a protein tyrosine kinase 7 (PTK7) antibody-drug conjugate (ADC) with a topoisomerase I inhibitor as payload

Cannot have received: topoisomerase I-based antibody-drug conjugate

Prior topoisomerase I-based ADCs are not allowed in cohorts A2, B1 or B2

Lab requirements

Cardiac function

Significant cardiovascular disease; QTcF > 470 ms

Significant cardiovascular disease. Prolongation of QT interval corrected for heart rate using Fridericia's formula (QTcF) > 470 milliseconds (ms)

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

US trial sites

  • Stanford Medicine Cancer Center · Stanford, California
  • Florida Cancer Specialists - Lake Nona - Sarah Cannon Research Institute · Orlando, Florida
  • Florida Cancer Specialists - Sarasota · Sarasota, Florida
  • The University of Chicago Medical Center (UCMC) · Chicago, Illinois
  • Community Health Network · Indianapolis, Indiana

Showing up to 5 US sites.

See all sites on ClinicalTrials.gov →

Frequently asked questions

Is NCT07046923 currently recruiting?

Yes, this trial is currently recruiting patients.

Are there prior therapy exclusions?

Yes. Prior protein tyrosine kinase 7 antibody-drug conjugate with topoisomerase I inhibitor payload, topoisomerase I-based antibody-drug conjugate disqualifies patients from enrollment.

Does this trial require EGFR?

Yes, EGFR wild-type is a required biomarker for enrollment.

Does this trial require ALK?

Yes, ALK wild-type is a required biomarker for enrollment.

Does this trial require ROS1?

Yes, ROS1 wild-type is a required biomarker for 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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