TrialSignal
Clinical trial intelligence report
A Phase IIB, Randomized, Double-Blinded, Placebo-Controlled Study of Low Dose Cytarabine and Lintuzumab Compared to Low Dose Cytarabine and Placebo in Patients 60 Years of Age and Older With Previously Untreated AML
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT00528333-Jul 28, 2026
NCT ID
NCT00528333
Status
COMPLETED
Phase
Phase 2
Sponsor
Seagen Inc.
Executive brief
Investment-Ready Snapshot
Seagen Inc. is investigating lintuzumab (SGN-33) in combination with low dose cytarabine for the treatment of acute myeloid leukemia (AML) in older patients who have declined intensive chemotherapy. The study targets a significant patient population, particularly those over 60 years of age, who are often underrepresented in clinical trials. If successful, this combination therapy could provide a new treatment option in a market characterized by limited therapies for elderly AML patients. The competitive landscape includes other therapies targeting AML, but lintuzumab's mechanism of action as a monoclonal antibody targeting CD33 may offer a differentiated approach. Diligence should focus on the safety profile, overall survival data, and potential regulatory pathways given the unmet need in this demographic.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT00528333
Indication
Acute Myeloid Leukemia
Modality
small molecule
Target
CD33 antigen expressed on leukemic blasts
Intervention
Lintuzumab (SGN-33), Low dose cytarabine, Placebo
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.