A Trial of AMXI-5001 for Treatment in Patients With Advanced Malignancies
Start Date
8/12/2020
Completion Date
10/1/2026
Summary
ATLAS-101 is a Phase I/II clinical trial of AMXI-5001 in adult participants with advanced malignancies who have previously failed other therapies. The study has two phases. The purpose of Phase I (Dose Escalation) is to confirm the appropriate treatment dose and Phase II (Dose Expansion) is to characterize the safety and efficacy of AMXI-5001.
Detailed Description
AMXI-5001 is an orally available dual PARP (poly adenosine diphosphate \[ADP\] ribose polymerase) and microtubule polymerization inhibitor. ATLAS-101 is a Phase I/II, open label, multi-center, non-randomized Dose Escalation and Dose Expansion study in participants with advanced malignancies. Study enrollment is approximately 122 participants. All participants receive oral AMXI-5001, twice daily, as monotherapy. Following Phase I (Dose Escalation) to identify the Maximum Tolerated Dose and the Recommended Dose for use in Phase II, additional participants will be enrolled into the Dose Expansion Phase to further characterize the safety, pharmacology, and clinical efficacy of AMXI-5001.
Eligibility Criteria
Age Range: 18 years to No maximum
Interventions
AMXI-5001:Dose Escalation Phase I
AMXI-5001:Dose Expansion Phase II
Conditions
Locations
University of California, Los Angles (UCLA) Department of Medicine - Hematology/Oncology
Los Angeles, California 90404
United States
Johns Hopkins
Baltimore, Maryland 21218
United States
SCRI Oncology Partners
Nashville, Tennessee 37203
United States
The University of Texas MD Anderson Cancer Center
Houston, Texas 77030
United States