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Study of Pembrolizumab + Pemetrexed + Platinum Chemotherapy With or Without Zoldonrasib as First Line Treatment in Metastatic Non-squamous RAS G12D-Mutated NSCLC

RECRUITINGPhase 3Sponsored by Revolution Medicines, Inc.
Actively Recruiting
PhasePhase 3
SponsorRevolution Medicines, Inc.
Started2026-08-14
Est. completion2029-10
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations1 site

Summary

The purpose of this study is to evaluate the efficacy of an investigational RAS(ON) inhibitor administered in combination with pembrolizumab and platinum-based chemotherapy doublet compared to placebo in combination with pembrolizumab and platinum-based chemotherapy doublet.

Eligibility

Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria:

* At least 18 years old and has provided informed consent.
* Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
* Histologically or cytologically confirmed, previously untreated metastatic non-squamous NSCLC.
* Known PD-L1 status
* Documented RAS G12D mutation status.
* Measurable disease per RECIST v1.1.
* Adequate organ function (bone marrow, liver, kidney, coagulation, thyroid).
* Able to take oral medications.

Exclusion Criteria:

* Prior treatment with systemic anticancer therapy in metastatic setting for NSCLC.
* Prior systemic therapy with any RAS-directed therapy.
* Untreated (symptomatic or asymptomatic) central nervous system metastatic disease.
* Any conditions that may affect the ability to take or absorb study drug.
* Major surgery on or within 28 days prior to randomization.
* Patient is unable or unwilling to comply with protocol-required study visits or procedures.
* Additional inclusion and exclusion criteria may apply

Conditions9

CancerLung CancerLung Cancer (NSCLC)Metastatic NSCLC - Non-Small Cell Lung CancerMetastatic Non-squamous Non Small Cell Lung CancerNSCLCNon Small Cell Lung CancerNon-Squamous Non-Small Cell Lung CancerNon-small Cell Lung Cancer (NSCLC)

Interventions3

Locations1 site

Florida Clinical Trials Group, LLC
Plantation, Florida, 33322
Sandra Perez772-297-3057perezs@floridactg.com

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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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