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Clinical trial intelligence report
A Phase I, Open-Label, Dose Escalation and Cohort Expansion Study of BS HH 002.SA in Patients With Acute Myeloid Leukemia (AML) and Myelodysplastic Syndrome (MDS)
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 13, 2026
NCT ID
NCT04743115
Status
UNKNOWN
Phase
Phase 1
Sponsor
Shanghai Bensen Pharmaceutical Co., Ltd.
Executive brief
Investment-Ready Snapshot
BS HH 002.SA is being developed by Shanghai Bensen Pharmaceutical Co., Ltd. for the treatment of relapsed or refractory Acute Myeloid Leukemia (AML) and high-risk Myelodysplastic Syndrome (MDS). The target patient population is significant due to the limited treatment options available for these conditions, suggesting a potentially lucrative market. The study's design includes a dose escalation and cohort expansion, indicating a strategic approach to establishing safety and efficacy. The competitive landscape includes other emerging therapies for AML and MDS, necessitating diligent monitoring of similar clinical trials and market entrants. The trial's current status is 'Not Yet Recruiting,' which may impact timelines for market entry and revenue generation.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT04743115
Indication
Acute Myeloid Leukemia, Myelodysplastic Syndrome
Modality
small molecule
Target
Not specified in the provided data; further investigation required to identify the precise molecular or mechanistic target profile of BS HH 002.SA.
Intervention
BS HH 002.SA
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.