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Clinical Trial Summary

This study evaluates the safety and tolerability of escalating doses of BP1002 (Liposomal Bcl-2 Antisense Oligodeoxynucleotide) in patients with refractory/relapsed AML. The study is designed to assess the safety profile, identify DLTs, biologically effective doses, PK, PD and potential anti-leukemic effects of BP1002 as single agent (dose escalation phase) followed by assessing BP1002 in combination with decitabine (dose expansion phase).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT05190471
Study type Interventional
Source Bio-Path Holdings, Inc.
Contact Michael Hickey
Phone 832-742-1361
Email [email protected]
Status Not yet recruiting
Phase Phase 1
Start date January 2022
Completion date September 2024

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