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Clinical trial intelligence report
A Phase 1 Study of AC220 (ASP2689) as Maintenance Therapy in Subjects With Acute Myeloid Leukemia Who Have Been Treated With an Allogeneic Hematopoietic Stem Cell Transplant
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT01468467-Jul 28, 2026
NCT ID
NCT01468467
Status
COMPLETED
Phase
Phase 1
Sponsor
Daiichi Sankyo
Executive brief
Investment-Ready Snapshot
AC220 (ASP2689), developed by Daiichi Sankyo, is positioned as a maintenance therapy for patients with Acute Myeloid Leukemia (AML) post-allogeneic hematopoietic stem cell transplant. The market for AML therapies is growing, driven by increasing incidence rates and the need for improved post-transplant management options. The competitive landscape includes other FLT3 inhibitors, such as quizartinib, which may pose a challenge. Successful outcomes from this trial could enhance Daiichi Sankyo's portfolio in hematologic malignancies and provide a strategic advantage in the post-transplant AML treatment space. Diligence should focus on the safety profile and potential market access strategies, considering the evolving regulatory environment for oncology therapies.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT01468467
Indication
Leukemia, Myeloid, Acute
Modality
small molecule
Target
FMS-like tyrosine kinase 3 (FLT3)
Intervention
AC220
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.