Drug intelligence / Profile preview

BS-002

Development stage
Phase 1
Lead developer
Shanghai Bensen Pharmaceutical
Modality
Small Molecules
Administration
Subcutaneous
01

Overview

BS-002 (also known as BS HH 002.SA) is a small molecule protein synthesis inhibitor being developed by Shanghai Bensen Pharmaceutical for the treatment of myeloid malignancies, including relapsed or refractory acute myeloid leukemia (AML) and high-risk myelodysplastic syndrome (MDS). The drug is a subcutaneous formulation of homoharringtonine (also known as omacetaxine mepesuccinate), a plant alkaloid that interferes with the elongation step of protein translation. By binding to the A-site of the 60S ribosomal subunit, BS-002 prevents the correct positioning of aminoacyl-tRNA, leading to the rapid depletion of short-lived proteins essential for leukemic cell survival, such as the anti-apoptotic protein Mcl-1. The subcutaneous delivery route is intended to offer improved patient convenience and potentially a more favorable pharmacokinetic profile compared to traditional intravenous infusions of the same active ingredient.

Other names
subcutaneous homoharringtoninesubcutaneous omacetaxine mepesuccinate
02

Targets

JAK2 (Janus kinase 2)MCL1 (Myeloid cell leukemia sequence 1)

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