TrialSignal
Clinical trial intelligence report
A Phase IIa, Open-label, Clinical Trial to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Efficacy of BP1001 (a Liposomal Grb2 Antisense Oligonucleotide) in Combination With Venetoclax Plus Decitabine in Patients With AML Who Are Ineligible for Intensive Induction Therapy
Source-linked diligence brief with registry provenance, taxonomy normalization and premium analytical context.
Generated
Jun 20, 2026
NCT ID
NCT02781883
Status
RECRUITING
Phase
Phase 2a
Sponsor
Bio-Path Holdings, Inc.
Executive brief
Investment-Ready Snapshot
Bio-Path Holdings, Inc. is advancing BP1001, a liposomal Grb2 antisense oligonucleotide, in a Phase 2a clinical trial targeting acute myeloid leukemia (AML) patients who are ineligible for intensive induction therapy. The combination of BP1001 with venetoclax and decitabine aims to enhance efficacy compared to historical controls. The AML market is characterized by a high unmet need, particularly for patients unable to tolerate aggressive chemotherapy. If successful, BP1001 could position Bio-Path favorably against established therapies, potentially capturing a significant share of the AML treatment landscape. The trial's design includes multiple cohorts, allowing for flexibility in patient selection and treatment optimization, which may enhance the asset's attractiveness to potential partners or acquirers.
Source & freshness
Provenance
https://clinicaltrials.gov/study/NCT02781883
Indication
Acute Myeloid Leukemia (AML)
Modality
combination therapy
Target
Growth Factor Receptor-Bound Protein 2 (Grb2)
Intervention
BP1001 in combination with Ventoclax plus decitabine, BP1001 plus decitabine
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.