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Study details
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Personalized Antibody-Drug Conjugate Therapy Based on RNA and Protein Testing for the Treatment of Advanced or Metastatic Solid Tumors (The ADC MATCH Screening and Treatment Trial)

National Cancer Institute (NCI)
NCT IDNCT06311214ClinicalTrials.gov data as of Apr 2026
Phase

Phase 2

Target enrollment

500

Study length

about 3 years

Ages

18+

Locations

27 sites in CA, CT, FL +12

What this study is about

This trial is testing whether biomarker-directed treatment with one of three antibody-drug conjugates (ADCs) works in treating patients with solid tumor cancers that have high expression of the Trop-2, nectin-4, or HER2 proteins. The goal is to determine if personalized treatment with sacituzumab govitecan, enfortumab vedotin, or trastuzumab deruxtecan may be an effective option for patients with advanced or metastatic solid tumors that screen positive for high expression of Trop-2, nectin-4, or HER2, respectively.

Simplified from trial records by PatientMatch.

What you may be asked to do

  • 1.Electronic Health Record Review
  • 2.Immunohistochemistry Staining Method
  • 3.Receive Sacituzumab Govitecan
  • +3 more

Participation Burden

What's physically and logistically required of participants.

Logistics & Travel
In-person visits

Requires travel to a study site

Physical Intervention
Injection / IV

How treatment is administered

Treatment Assignment
All receive treatment

Everyone gets the investigational treatment.

Extracted study details

Pulled from the trial record to show what is being tested and what the study is measuring.

Drug classes

enfortumab vedotin, sacituzumab govitecan, trastuzumab deruxtecan

Drug routes

infusion

Endpoints

Primary: Frequency of high protein expression in patients with high ribonucleic acid (RNA) expression of each antibody-drug conjugate target (screening protocol), Objective response rate (treatment cohorts)

Secondary: Incidence of adverse events (treatment cohorts), Overall survival (treatment cohorts), Pharmacodynamic changes in the tumor and microenvironment (treatment cohorts), Progression free survival (treatment cohorts), Time to progression (treatment cohorts)

Procedures

biopsy, diagnostic, imaging