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A Study to Learn About Study Medicine ALTA2618 in Adults With AKT1 E17K-Mutant Solid Tumors
Trial Status: active
The purpose of this study is to characterize the safety and tolerability of ALTA2618 in
adults with AKT1 E17K-mutant advanced solid tumors.
Inclusion Criteria
Histologically confirmed diagnosis of a solid tumor malignancy harboring AKT1 E17K mutation identified through molecular testing (NGS- or PCR-based) with a Clinical Laboratory Improvement Amendments-certified (or equivalent) diagnostic test.
Unresectable or metastatic disease
Progressed on, intolerant to, or declined prior standard-of-care therapy (including targeted therapy, if applicable) appropriate to tumor type and stage
Evaluable or measurable disease per RECIST v1.1
Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
Adequate organ function.
Exclusion Criteria
Prior treatment with PI3K and/or mTOR inhibitors
Patients known to have KRAS, NRAS, HRAS, or BRAF genomic alterations in their tumor
Known condition that prohibits ability to swallow or absorb an oral medication Other inclusion/exclusion criteria may apply.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06533059.
Locations matching your search criteria
United States
California
La Jolla
UC San Diego Moores Cancer Center
Status: Active
Name Not Available
Georgia
Atlanta
Emory University Hospital/Winship Cancer Institute
Status: Active
Name Not Available
Massachusetts
Boston
Brigham and Women's Hospital
Status: Active
Name Not Available
Dana-Farber Cancer Institute
Status: Active
Name Not Available
Massachusetts General Hospital Cancer Center
Status: Active
Name Not Available
Missouri
Saint Louis
Siteman Cancer Center at Washington University
Status: Active
Name Not Available
Texas
Houston
M D Anderson Cancer Center
Status: Active
Name Not Available
Wisconsin
Madison
University of Wisconsin Carbone Cancer Center - University Hospital
Status: Active
Name Not Available
This is an open-label, multicenter, Phase 1/1b study of ALTA2618, a mutant-selective and
orally bioavailable AKT1 E17K inhibitor, in adults with AKT1 E17K-mutant solid tumors.
This study will evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary
clinical activity of ALTA2618, and aims to find the best dose. The study consists of two
parts: Part 1 - Dose Escalation and Part 1b - Dose Expansion.