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Terminated Phase 1 Interventional

A Phase 1 Study of MRTX0902 in Solid Tumors With Mutations in the KRAS MAPK Pathway

ClinicalTrials.gov ID: NCT05578092

Public ClinicalTrials.gov record NCT05578092. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 7:19 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 1 Multiple Expansion Cohort Trial of the SOS1 Inhibitor MRTX0902 in Patients With Advanced Solid Tumors Harboring Mutations in the KRAS MAPK Pathway

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase 1, open-label, multicenter, study evaluating the safety, tolerability, PK, PD, and anti-tumor activity of MRTX0902 alone and in combination with MRTX849 (adagrasib) in patients with advanced solid tumor malignancy harboring mutations in the KRAS-MAPK pathways.

Study identification

NCT ID
NCT05578092
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Mirati Therapeutics Inc.
Industry
Enrollment
64 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2, 2022 (Actual)
Primary completion
Feb 3, 2026 (Actual)
Completion
Feb 3, 2026 (Actual)
Last update posted
Feb 19, 2026

2022 – 2026

United States locations

U.S. sites
17
U.S. states
13
U.S. cities
16
Facility City State ZIP Site status
Local Institution - 001-108 New Haven Connecticut 06520 —
Local Institution - 001-119 Newark Delaware 19713-2055 —
Local Institution - 001-111 Orlando Florida 32827-7400 —
Local Institution - 001-103 Baltimore Maryland 21287 —
Local Institution - 001-110 Rochester Minnesota 55905-0001 —
Local Institution - 001-115 Hackensack New Jersey 07601-2191 —
Local Institution - 001-106 Cincinnati Ohio 45219-2364 —
Local Institution - 001-109 Portland Oregon 97239-3011 —
Local Institution - 001-116 Pittsburgh Pennsylvania 15232 —
Local Institution - 001-101 Nashville Tennessee 37203 —
Local Institution - 001-102 Nashville Tennessee 37203 —
Local Institution - 001-112 Dallas Texas 75246-2003 —
Local Institution - 001-122 Fort Worth Texas 76104-2154 —
Local Institution - 001-107 Houston Texas 77030 —
Local Institution - 001-123 Tyler Texas 75708-3154 —
Local Institution - 001-104 Fairfax Virginia 22031 —
Local Institution - 001-105 Seattle Washington 98109 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 1 non-U.S. site.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05578092, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 19, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05578092 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →