Overview

Phase 1-2 Study of ASTX660 in Subjects With Advanced Solid Tumors and Lymphomas

Status:
Recruiting
Trial end date:
2022-05-01
Target enrollment:
Participant gender:
Summary
This is an open-label, dose-escalation Phase 1/2 study to assess the safety of ASTX660, determine the maximum tolerated dose (MTD), recommended Phase 2 dose (RP2D), and recommended dosing regimen, and to obtain preliminary efficacy, pharmacokinetic (PK), and target engagement data, in subjects with advanced solid tumors or lymphoma for whom standard life-prolonging measures are not available.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Astex Pharmaceuticals
Astex Pharmaceuticals, Inc.