TrialSignal
Clinical trial intelligence report
A Phase II Study of Gemtuzumab Ozogamicin (Mylotarg) and Standard Dose ARA-C for Patients With Relapsed Acute Myeloid Leukemia (AML)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Aug 04, 2026
Report code
NCT00049179-Aug 04, 2026
NCT ID
NCT00049179
Status
COMPLETED
Phase
Phase 2
Sponsor
SWOG Cancer Research Network
Executive brief
Investment-Ready Snapshot
The Phase II study of Gemtuzumab Ozogamicin (Mylotarg) combined with standard dose cytarabine targets relapsed acute myeloid leukemia (AML) patients, specifically those with CD33-positive tumors. Given the high unmet medical need in relapsed AML, successful outcomes could position this combination therapy as a competitive treatment option in a market characterized by limited effective therapies. The collaboration with SWOG Cancer Research Network and the National Cancer Institute (NCI) enhances credibility and may facilitate further development or regulatory pathways. The market for AML therapies is growing, driven by increasing incidence rates and advancements in personalized medicine, suggesting potential for significant commercial returns if the trial demonstrates efficacy and safety.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00049179
Indication
Leukemia
Modality
small molecule
Target
CD33-positive acute myeloid leukemia (AML) cells
Intervention
cytarabine, gemtuzumab ozogamicin
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.