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Clinical Trial Summary

A Phase I Combination Study of CYC065 and Venetoclax for Relapsed or Refractory Chronic Lymphocytic Leukemia (CLL)


Clinical Trial Description

This is an open-label, single arm, dose escalation study in patients with relapsed or refractory CLL. Treatment will be administered on an outpatient basis and all patients will receive CYC065 over 4-hour infusion once every 2 weeks on Day 1 and Day 15 in combination with venetoclax. One treatment cycle is 4 weeks. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03739554
Study type Interventional
Source Cyclacel Pharmaceuticals, Inc.
Contact
Status Completed
Phase Phase 1
Start date January 25, 2019
Completion date April 27, 2023

See also
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