Drug intelligence / Profile preview

gemcitabine + nab-paclitaxel + dociparstat

Development stage
Preclinical
Lead developer
Bristol Myers Squibb
Modality
Nanoparticles → Drug Delivery Systems, Small Molecules
Administration
Intravenous
01

Overview

**Gemcitabine + nab-paclitaxel + dociparstat** is an investigational combination therapy comprising three components: gemcitabine, nab-paclitaxel, and dociparstat. - **Gemcitabine** is a nucleoside analog that interferes with DNA synthesis and induces cell death in rapidly dividing cells. - **Nab-paclitaxel** is paclitaxel bound to albumin nanoparticles, which enhances tumor delivery and reduces hypersensitivity reactions compared to conventional formulations[1][6]. - **Dociparstat** is a heparin derivative with the 2-O and 3-O sulfate groups removed, resulting in no anticoagulant activity and under investigation for its potential anti-inflammatory and anti-tumor properties[3]. This combination is experimental and has been explored in preclinical/early phase settings for the treatment of pancreatic cancer, with each component contributing cytotoxic or tumor microenvironment-modulating effects. The combination is not an approved standard regimen; nab-paclitaxel and gemcitabine are approved as a doublet for metastatic pancreatic cancer, while dociparstat addition is investigational.

02

Targets

TUBB (Tubulin (alpha and beta subunits))DNACXCR4 (C-X-C motif chemokine receptor 4)RNR (Ribonucleotide reductase)

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