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OncoMatch/Clinical Trials/NCT06440005

A Study to Evaluate Safety, Tolerability and Preliminary Activity of AGX101 in Participants With Advanced Solid Tumors

Is NCT06440005 recruiting? Yes, currently enrolling (May 2026). This Phase 1 trial studies AGX101 for cancer.

Phase 1RecruitingAngiex, Inc.NCT06440005Data as of May 2026

Treatment: AGX101AGX101 is an antibody-drug conjugate (ADC) therapy for tumor-forming cancers. The purpose of this study is to learn about AGX101 effects and safety at various dose levels in an all-comers advanced solid cancer patient population. AGX101will be administered intravenously. Dosing of AGX101 will be repeated once every 3, 6 or 9 weeks. Participants may continue study treatment until disease progression, unacceptable toxicity, or consent withdrawal. Subjects will attend an end of treatment visit and will receive two safety follow-up telephone contacts up to 90 days following the last dose of study drug.

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Extracted eligibility criteria

Cancer type

Tumor Agnostic

Breast Carcinoma

Prostate Cancer

Colorectal Cancer

Pancreatic Cancer

Hepatocellular Carcinoma

Sarcoma

Performance status

ECOG 0–1(Restricted strenuous activity)

Lab requirements

Blood counts

adequate organ function

Kidney function

adequate organ function

Liver function

adequate organ function

Cardiac function

LVEF  50%, as determined on cardiac ECHO or cardiac multiple-gated acquisition (MUGA) scan

Have adequate organ function; LVEF  50%, as determined on cardiac ECHO or cardiac multiple-gated acquisition (MUGA) scan

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

US trial sites

  • USC/Norris Comprehensive Cancer Center · Los Angeles, California
  • Florida Cancer Specialist · Sarasota, Florida
  • Washington University School of Medicine · St Louis, Missouri
  • Sarah Cannon Research Center · Nashville, Tennessee
  • NEXT Oncology · San Antonio, Texas

Showing up to 5 US sites. See all sites on ClinicalTrials.gov →

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