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CC-486 and Venetoclax for Acute Myeloid Leukemia - Trial NCT05287568

Access comprehensive clinical trial information for NCT05287568 through Pure Global AI's free database. This Phase 1 trial is sponsored by University of Colorado, Denver and is currently Recruiting. The study focuses on AML. Target enrollment is 22 participants.

This page provides complete trial specifications, intervention details, outcomes, and location information. Pure Global AI offers free access to ClinicalTrials.gov data, helping medical device and pharmaceutical companies navigate clinical research efficiently.

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NCT05287568
Phase 1
Recruiting
drug
Trial Details
ClinicalTrials.gov โ€ข NCT05287568
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CC-486 and Venetoclax for Acute Myeloid Leukemia

Study Focus

AML

Venetoclax

Interventional

drug

Sponsor & Location

University of Colorado, Denver

Aurora,Aurora, United States of America

Timeline & Enrollment

Phase 1

Mar 15, 2022

Mar 01, 2029

22 participants

Primary Outcome

Determine the maximum tolerated dose of CC-486 in combination with venetoclax

Summary

This is an open label, dose escalation Phase I single institution pilot study for relapsed
 and refractory AML patients using CC-486 (oral azacitidine) with venetoclax. At the
 completion of dose escalation and after establishment of the MTD or recommended dose of
 CC-486 with venetoclax, an expansion phase will commence, using venetoclax with the MTD of
 CC-486 in relapsed/refractory patients.

ICD-10 Classifications

Acute myeloblastic leukaemia [AML]

Data Source

ClinicalTrials.gov

NCT05287568

Non-Device Trial