TrialSignal
Clinical trial intelligence report
High-Dose Ara-C Followed by Continuous Infusion Interleukin-2 for Acute Myelogenous Leukemia in First Remission
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00136448-Jul 28, 2026
NCT ID
NCT00136448
Status
COMPLETED
Phase
Phase 2
Sponsor
Dana-Farber Cancer Institute
Executive brief
Investment-Ready Snapshot
The study conducted by Dana-Farber Cancer Institute investigates the combination of high-dose ara-C and continuous infusion IL-2 in patients with AML in first remission. Given the high unmet need in AML treatment, particularly for patients in remission, this trial could provide valuable data on the efficacy and safety of this combination therapy. The results may position Dana-Farber as a leader in innovative AML therapies, potentially attracting partnerships or investments. The competitive landscape includes established therapies such as chemotherapy and emerging immunotherapies, necessitating a thorough analysis of clinical outcomes to assess market positioning. The findings could influence future treatment guidelines and reimbursement strategies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00136448
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
Interleukin-2 (IL-2) and cytarabine (ara-C) in the treatment of Acute Myelogenous Leukemia (AML)
Intervention
cytosine arabinoside (ara-C), daunomycin, interleukin-2
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.