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NCT04743115UNKNOWNanonymous

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)

Sponsor

Source record

Shanghai Bensen Pharmaceutical Co., Ltd.

Phase

Source record

Phase 1

Modality

AI-normalized

small molecule

Target

AI-normalized

Not specified in the provided data; further investigation required to identify the precise molecular or mechanistic target profile of BS HH 002.SA.

Indication / condition

AI-normalized

Acute Myeloid Leukemia, Myelodysplastic Syndrome

Intervention

Source record

BS HH 002.SA

Source & freshness

Source record

NCT ID

NCT04743115

Original source

ClinicalTrials.gov

Source last updated

Feb 08, 2021

Ingested at

Jun 12, 2026

Internal sync

Jun 12, 2026

Model version

trialsignal-ai-v1

Normalized confidence

96%

Validation status

validated

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View original source fields

NCT ID

NCT04743115

Title

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)

Sponsor

Shanghai Bensen Pharmaceutical Co., Ltd.

Status

UNKNOWN

Phase

Phase 1

Condition raw

Acute Myeloid Leukemia, Myelodysplastic Syndrome

Condition normalized

Acute Myeloid Leukemia, Myelodysplastic Syndrome

Modality raw

small molecule

Modality normalized

small molecule

Target raw

Not specified in the provided data; further investigation required to identify the precise molecular or mechanistic target profile of BS HH 002.SA.

Target normalized

Not specified in the provided data; further investigation required to identify the precise molecular or mechanistic target profile of BS HH 002.SA.

Interventions

BS HH 002.SA

Public preview

Source record

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.

AI-generated analysis supports research triage only. Verify source records, publications, sponsor disclosures and IP databases before making diligence decisions. Model: trialsignal-ai-v1.

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