TrialSignal
Clinical trial intelligence report
A Phase 1 Study of ICP-248 in Combination With Azacitidine for the Treatment in Patients With Myeloid Malignancies.
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jul 28, 2026
Report code
NCT06656494-Jul 28, 2026
NCT ID
NCT06656494
Status
RECRUITING
Phase
Phase 1
Sponsor
Beijing InnoCare Pharma Tech Co., Ltd.
Executive brief
Investment-Ready Snapshot
Beijing InnoCare Pharma Tech Co., Ltd. is advancing ICP-248 in combination with azacitidine for the treatment of acute myelogenous leukemia (AML) and myelodysplastic syndromes (MDS). The trial is currently recruiting participants across multiple sites in the United States and China, indicating a robust geographical strategy to capture diverse patient populations. The market for AML and MDS therapies is competitive, with established players like Celgene and Novartis. Successful outcomes from this trial could position InnoCare favorably within this landscape, particularly if ICP-248 demonstrates superior safety and efficacy profiles compared to existing treatments. The estimated completion of the trial in early 2028 suggests a long-term investment horizon, with potential implications for future market entry and revenue generation.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT06656494
Indication
Acute Myelogenous Leukemia
Modality
small molecule
Target
ICP-248 is a novel therapeutic agent targeting myeloid malignancies, potentially acting through mechanisms that enhance the efficacy of azacitidine, a known hypomethylating agent.
Intervention
ICP-248, Azacitidine
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.