TrialSignal
Clinical trial intelligence report
Phase I/II Study of Plerixafor and Clofarabine in Previously Untreated Older (>/=60 Years) Adult Patients With Acute Myelogenous Leukemia (AML) With Two or More Unfavorable Prognostic Factors for Whom Standard Induction Chemotherapy is Unlikely to be of Benefit
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01160354-Jul 28, 2026
NCT ID
NCT01160354
Status
TERMINATED
Phase
PHASE1
Sponsor
M.D. Anderson Cancer Center
Executive brief
Investment-Ready Snapshot
Phase I/II Study of Plerixafor and Clofarabine in Previously Untreated Older (>/=60 Years) Adult Patients With Acute Myelogenous Leukemia (AML) With Two or More Unfavorable Prognostic Factors for Whom Standard Induction Chemotherapy is Unlikely to be of Benefit is a PHASE1 clinical asset sponsored by M.D. Anderson Cancer Center in Acute Myelogenous Leukemia. SEO and diligence focus: Plerixafor, Clofarabine, endpoint relevance, enrollment feasibility, competitive positioning, readout timing and IP durability.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01160354
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
Plerixafor, Clofarabine
Intervention
Plerixafor, Clofarabine
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.