Overview

A Study to Investigate CYC140, in Subjects With Advanced Solid Tumors and Lymphoma

Status:
Recruiting
Trial end date:
2025-11-01
Target enrollment:
Participant gender:
Summary
This is a 2-part, phase 1/2, open-label, multicenter study designed to evaluate the safety, tolerability, pharmacokinetics, pharmacodynamics, pharmacogenomics, and efficacy of CYC140 administered orally daily. This study consists of Phase 1 and Phase 2 components in subjects with advanced solid tumors and lymphoma who have progressed despite having standard therapy or for which no standard therapy exists.
Phase:
Phase 1/Phase 2
Details
Lead Sponsor:
Cyclacel Pharmaceuticals, Inc.