RecruitingPhase 1NCT07066657

A Study of MRG007 (ARR-217) in Patients With Advanced Solid Tumors

An Open-Label, Multi-Center, Dose Escalation, Confirmation, and Expansion Phase I Clinical Study to Evaluate the Safety, Tolerability, Efficacy, and Pharmacokinetics of MRG007 (ARR-217) in Participants With Unresectable Locally Advanced or Metastatic Solid Tumors


Sponsor

ArriVent BioPharma, Inc.

Enrollment

405 participants

Start Date

Jul 25, 2025

Study Type

INTERVENTIONAL

Conditions

Summary

This is an open-label, multi-center, phase I study to evaluate the safety, tolerability, efficacy, and pharmacokinetics of MRG007 (ARR-217) in patients with unresectable locally advanced or metastatic solid tumors.


Eligibility

Min Age: 18 Years

Plain Language Summary

Simplified for easier understanding

This study is testing a new drug called MRG007 (also called ARR-217) — an antibody-drug conjugate that targets a protein called CDH17 found on certain cancer cells — in people with advanced solid tumors that have not responded to standard treatments. **You may be eligible if...** - You have been diagnosed with an advanced or metastatic solid tumor that failed standard treatment options - Your tumor has been tested (or you agree to a biopsy) for CDH17, the protein the drug targets - You have at least one measurable tumor on imaging - You are in good to fair physical condition - Your liver, kidneys, and blood counts are in acceptable range **You may NOT be eligible if...** - You have more than one type of cancer - You have previously received a CDH17-targeting therapy - You have active hepatitis B or C, or HIV infection - You have significant heart or lung disease - You have uncontrolled fluid buildup around your heart, lungs, or abdomen Talk to your doctor to see if this trial is right for you.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGMRG007

MRG007 will be administrated as specified in the protocol.


Locations(15)

ULCA

Los Angeles, California, United States

UCSF

San Francisco, California, United States

University of Colorado

Aurora, Colorado, United States

Sarah Cannon Research Institute

Denver, Colorado, United States

Sarah Cannon Research Institute

Sarasota, Florida, United States

Sarah Cannon Research Institute

Nashville, Tennessee, United States

MD Anderson Cancer Center

Houston, Texas, United States

NEXT Dallas

Irving, Texas, United States

NEXT Virginia

Fairfax, Virginia, United States

Fred Hutchinson Cancer Center

Seattle, Washington, United States

Peking University Cancer Hospital

Beijing, Beijing Municipality, China

Union Hospital, Tongji Medical College, Huazhong University of Science and Technology

Wuhan, Hubei, China

Hunan Cancer Hospital

Changsha, Hunan, China

Renji Hospital Shanghai Jiaotong University School of Medicine

Shanghai, Shanghai Municipality, China

Zhongshan Hospital Fudan University

Shanghai, Shanghai Municipality, China

View Full Details on ClinicalTrials.gov

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NCT07066657


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