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Clinical trial

A Phase 1/2, Open-label, Multicenter Dose Escalation and Dose Expansion Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of CC-90011 in Combination With Venetoclax and Azacitidine in R/R Acute Myeloid Leukemia (AML) and Treatment-naïve Subjects With AML Who Are Not Eligible for Intensive Induction Chemotherapy

NCT04748848 is registered in ClinicalTrials.gov with Celgene as lead sponsor.

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Registry record

As filed in ClinicalTrials.gov.

Title
A Phase 1/2, Open-label, Multicenter Dose Escalation and Dose Expansion Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of CC-90011 in Combination With Venetoclax and Azacitidine in R/R Acute Myeloid Leukemia (AML) and Treatment-naïve Subjects With AML Who Are Not Eligible for Intensive Induction Chemotherapy
Lead sponsor
Celgene
Phase
Phase 1
Overall status
Terminated
Start date
October 14, 2021
Completion date
March 9, 2022
Enrollment
1 (actual)
Sites
17

Conditions

As the registry lists them; a condition with its own page is linked.