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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

  • Protocol Number: 202601115
  • Principal Investigator: Waqar, Saiama
  • Cancer Types: Lung

Learn more about this study at: clinicaltrials.gov

For more information on this trial, contact us here:

Phone
800-600-3606
Email
[email protected]

Brief Summary

The goal of this clinical trial is to learn about the safety and recommended dose of TRI-611 when administered to adults with ALK-positive non-small cell lung cancer (NSCLC). The trial will also evaluate the antitumor activity of TRI-611 in adults with ALK-positive NSCLC.

The study will be conducted in two parts. The first part will examine different doses of TRI-611. The second part will look at how well TRI-611 works on ALK-positive NSCLC when administered to three groups of participants that differ based on what type of prior therapy they have received.

In this study participants will:

* Take TRI-611 on a continued basis, provided it is well-tolerated, for as long as their disease is not progressing
* Visit the clinic approximately seven times in the first 3 months and then just once at the start of each 28-day cycle thereafter
* Keep a diary of each time they take the study medication

Protocol Interventions

Drug: TRI-611