TrialSignal
Clinical trial intelligence report
An Open-Label Phase Ib/II Study of Avelumab in Combination With 5-Azacytidine (Vidaza) for the Treatment of Patients With Refractory/Relapsed Acute Myeloid Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT02953561-Jul 28, 2026
NCT ID
NCT02953561
Status
TERMINATED
Phase
Phase 1/2
Sponsor
M.D. Anderson Cancer Center
Executive brief
Investment-Ready Snapshot
The combination of avelumab, a PD-L1 inhibitor, with azacitidine, an established treatment for acute myeloid leukemia (AML), targets a niche market of refractory/relapsed AML patients. The trial's termination due to a PDOL request indicates potential regulatory or strategic challenges. However, the data generated may provide insights into the immunological mechanisms of AML treatment, which could be leveraged for future product development or partnerships. The competitive landscape includes other PD-1/PD-L1 inhibitors and novel therapies for AML, necessitating a thorough diligence process to assess market positioning and potential collaborations.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02953561
Indication
Acute Myeloid Leukemia Arising From Previous Myelodysplastic Syndrome
Modality
small molecule
Target
PD-L1 (Programmed Death-Ligand 1)
Intervention
Avelumab, Azacitidine, Laboratory Biomarker Analysis
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.