Viewing Study NCT03484520


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Ignite Modification Date: 2025-12-26 @ 3:31 AM
Study NCT ID: NCT03484520
Status: TERMINATED
Last Update Posted: 2022-12-30
First Post: 2018-03-26
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: A Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Sponsor: AbbVie
Organization:

Study Overview

Official Title: Phase 1b Study of Venetoclax and Dinaciclib (MK7965) in Patients With Relapsed/Refractory Acute Myeloid Leukemia
Status: TERMINATED
Status Verified Date: 2022-12
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Strategic considerations
Has Expanded Access: True
If Expanded Access, NCT#: NCT03123029
Has Expanded Access, NCT# Status: AVAILABLE
Acronym: None
Brief Summary: An open-label, dose-escalation study to assess safety, pharmacokinetics and efficacy as well as determine the recommended Phase 2 doses of co-administered therapy of dinaciclib and venetoclax for patients with relapsed or refractory Acute Myeloid Leukemia (R/R AML).
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: True
Is a FDA Regulated Device?: False
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: False
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
2017-003213-26 EUDRACT_NUMBER None View