The purpose of this study is to characterize the safety and tolerability of ALTA2618 in
adults with AKT1 E17K-mutant advanced solid tumors.
Study sponsor and potential other locations can be found on ClinicalTrials.gov for NCT06533059.
Locations matching your search criteria
United States
Wisconsin
Madison
University of Wisconsin Carbone Cancer Center - University HospitalStatus: 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.
Lead OrganizationAlterome Therapeutics, Inc.