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A Solid Tumor Study for Long Term Treatment of Cancer Patients Who Participated in Adagrasib Studies

RECRUITINGPhase 2Sponsored by Mirati Therapeutics Inc.
Actively Recruiting
PhasePhase 2
SponsorMirati Therapeutics Inc.
Started2026-05-06
Est. completion2028-02-16
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations17 sites

Summary

This is an open-label, solid tumor, continuation, rollover trial which enrolls participants from ongoing BMS parent studies that evaluated adagrasib (MRTX849, BMS-986503) either as monotherapy or in combination with other cancer therapies in patients with non-small cell lung cancer (NSCLC), colorectal cancer (CRC) and other advanced solid tumors.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

* Participant is eligible to receive continued study treatment as per the parent study, and/or investigator assessed clinical benefit.
* Individuals with assigned female sex at birth (AFSB) must have documented proof that they are not of childbearing potential. IOCBP participants who are sexually active must agree to follow the instructions for method(s) of contraception and included in the ICF.

Exclusion Criteria:

* Participant is not eligible for study treatment per the parent study eligibility criteria.
* Participants who have completed treatment with the study drugs, progressed on prior study treatment, or discontinued study treatment due to toxicity in the parent study are not eligible to receive study drug in this study.
* Participants not receiving clinical benefit from parent study drug as assessed by the investigator.

Other protocol defined inclusion/exclusion criteria applies.

Conditions2

CancerSolid Tumors

Interventions9

Locations17 sites

Local Institution - 0005
Local Institution - 0016
Bellflower, California, 90706
Site 0016
Local Institution - 0082
Site 0082
Local Institution - 0003
Newark, Delaware, 19713
Local Institution - 0001
St. Petersburg, Florida, 33701
Site 0001

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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.

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