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Clinical trial intelligence report
A Phase II Randomized Trial of Immunologic and Chemotherapeutic Agents for Treatment of Patients With Relapsed or Refractory Acute Myelogenous Leukemia
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 18, 2026
NCT ID
NCT00005962
Status
COMPLETED
Phase
Phase 2
Sponsor
Eastern Cooperative Oncology Group
Executive brief
Investment-Ready Snapshot
This Phase II trial, sponsored by the Eastern Cooperative Oncology Group, investigates the efficacy of three treatment regimens for relapsed or refractory acute myelogenous leukemia (AML). The trial's completion in 2007 and subsequent publication of results in 2010 indicate that the study did not yield improved outcomes with the tested regimens. The competitive landscape for AML treatments includes established therapies and emerging agents, necessitating careful evaluation of this trial's findings against current standards of care. The market for AML therapies remains robust, with ongoing demand for innovative treatments, particularly for relapsed or refractory cases. Companies should consider the implications of these results on future development strategies and potential partnerships.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00005962
Indication
Leukemia
Modality
protein therapy
Target
CD33 positive acute myelogenous leukemia cells, utilizing monoclonal antibodies and chemotherapeutic agents.
Intervention
sargramostim, cyclophosphamide, cytarabine, gemtuzumab ozogamicin, liposomal daunorubicin citrate, topotecan hydrochloride
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.