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A Phase 2, Open-label, Randomized, Two-stage Clinical Study of Alvocidib in Patients With Relapsed/Refractory Acute Myeloid Leukemia Following Treatment With Venetoclax Combination Therapy
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT03969420-Jul 28, 2026
NCT ID
NCT03969420
Status
TERMINATED
Phase
Phase 2
Sponsor
Sumitomo Pharma America, Inc.
Executive brief
Investment-Ready Snapshot
The clinical trial for alvocidib, sponsored by Sumitomo Pharma America, Inc., was aimed at evaluating its efficacy in patients with relapsed or refractory acute myeloid leukemia (AML) following treatment with venetoclax combination therapy. However, the study was terminated due to a business decision on November 17, 2020, with the last patient follow-up completed by May 14, 2021. This termination indicates potential challenges in the commercial viability of alvocidib, particularly in a competitive landscape where other therapies for AML, including venetoclax, are gaining traction. The decision to halt development may reflect insufficient efficacy or safety data to support further investment, necessitating a thorough review of the competitive landscape and market positioning for alternative therapies targeting AML.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT03969420
Indication
Acute Myeloid Leukemia (AML)
Modality
small molecule
Target
Cyclin-dependent kinases (CDKs), specifically targeting CDK9.
Intervention
Alvocidib (flavopiridol) and cytarabine (Ara-C), Alvocidib (flavopiridol)
Source record
Protocol Description
Detailed source ingestion pending.
Source record
Outcome Measures
Detailed source ingestion pending.
Source record
Eligibility
Detailed source ingestion pending.
AI analysis
Known Results And Readout Context
Detailed source ingestion pending.
IP intelligence
Patent And IP Landscape
Detailed source ingestion pending.
Source record
Contacts
Detailed source ingestion pending.