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A Phase 1/2 Study of TRI-611 in ALK-Positive NSCLC

A Phase 1/2, Dose Escalation and Expansion Study of TRI-611, an Oral ALK Molecular Glue Degrader in Participants With Advanced ALK-Positive NSCLC

Open to all qualified participants

Phase

PHASE1, PHASE2

Enrollment

160 (est.)

Age range

18 Years to โ€”

Sex

ALL

Summary

The goal of this trial is to learn about the safety and recommended dose of TRI-611 in adults with ALK-positive non-small cell lung cancer (NSCLC), and to evaluate its antitumor activity. The study runs in two parts: a dose-finding part and an expansion part across three groups defined by prior therapy.

Conditions studied

ALK-positive NSCLCALK-Positive Lung CancerALK-positive Non-small Cell Lung Cancer

Sponsors

TRIANA Biomedicines, Inc.Lead

Study locations

University of Colorado Cancer Center

Aurora, Colorado

Kyle Concannon, MD, PRINCIPAL_INVESTIGATOR

Washington University Medical Center

St Louis, Missouri

Saiama Waqar, MD, PRINCIPAL_INVESTIGATOR

Memorial Sloan-Kettering Cancer Center

New York, New York

Memorial Sloan Kettering Cancer Center, CONTACT

Taylor Cancer Research Center

Maumee, Ohio

Stephanie Ambrose, CONTACT

SCRI Oncology Partners

Nashville, Tennessee

AskSarah, CONTACT

START Mountain Region

West Valley City, Utah

Olivia Darais, CONTACT

NEXT Virginia

Fairfax, Virginia

Alexander Spira, MD, PRINCIPAL_INVESTIGATOR