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Study identifier: NCT07204340 Synced from ClinicalTrials.gov · August 08, 2026
● Study status: Recruiting

TLN-372 in Advanced KRAS Mutant Solid Tumors

Condition: KRAS Mutant Solid Tumors  ·  Sponsor: Treeline Biosciences, Inc.

PhasePhase 1
Planned participants270
Who can joinAll sexes, 18 Years to no upper limit
Healthy volunteersNoCheck eligibility criteria ↓
Where11 locations · 4 countries

Interested? Contact the study team ↓

Sponsor, CRO or site team? See where this study is running → — listed sites, countries and recruiting context. Everything below is written for patients and caregivers.

About this study

The primary purpose of this study is to evaluate the safety, pharmacokinetics, and anti-tumor activity of TLN-372 as a single agent and in combination with other anti-tumor agents, in patients with advanced KRAS mutant solid tumors

This description comes directly from the study's public registry record.

Talk to the study team

Treeline Clinical Operations  ·  857-228-0050  ·  clinicaloperations@treeline.bio

There is no obligation to join — the study team can answer your questions about taking part.

Always discuss trial participation with your own doctor first.

Full eligibility criteria (exactly as the study team wrote them)

Inclusion Criteria: 1. Patients must have measurable disease at study entry. 2. Patients must have locally advanced or metastatic KRAS mutant solid tumors. 3. Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1. 4. Adequate organ function. Exclusion Criteria: 1. Patients must not have active brain metastases. 2. Patients must not have current or past history of central nervous system (CNS) involvement. 3. Patients must not have major surgery or severe trauma within 4 weeks prior to the start of the study. 4. Patients must not have any condition, including significant acute or chronic medical illness, active or uncontrolled infection, or the presence of laboratory abnormalities, that places patients at unacceptable risk of participating in this study. 5. Patients must not have clinically significant cardiovascular disease. 6. Pregnant or lactating. 7. Conditions that could affect drug absorption.

Reproduced word-for-word from the public registry record — the study team can answer questions about it.

Locations (11)

University of Alabama at BirminghamBirmingham, Alabama, United StatesRecruiting
Dana-Farber Cancer InstituteBoston, Massachusetts, United StatesRecruiting
START MidwestGrand Rapids, Michigan, United StatesRecruiting
Washington University Medical CampusSt Louis, Missouri, United StatesRecruiting
Memorial Sloan Kettering Cancer CenterNew York, New York, United StatesRecruiting
Sarah Cannon Research InstituteNashville, Tennessee, United StatesRecruiting
Peter MacCallum Cancer CentreMelbourne, Victoria, AustraliaRecruiting
Linear Clinical ResearchPerth, Western Australia, AustraliaRecruiting
Princess Margaret Cancer CentreToronto, Ontario, CanadaRecruiting
Hospital Universitary Vall d'HebronBarcelona, SpainRecruiting
START Madrid_Hospital Universitario HM Sanchinarro_CIOCCMadrid, SpainRecruiting

More studies in these areas

This study lists sites in the areas below. Each link shows other recruiting studies near that city, from the public registry record.

BirminghamBostonGrand RapidsSt Louis

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