Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
nLs-BG129 is a first-in-class targeted nanoliposomal peptide formulation designed for the treatment of advanced malignancies, specifically pancreatic ductal adenocarcinoma (PDAC). The drug consists of a synthetic peptide, BG129, which acts as a potent antagonist of the gastrin-releasing peptide receptor (GRPR). GRPR is a G protein-coupled receptor that is significantly overexpressed in various cancers, including pancreatic, prostate, and lung cancers, where it drives tumor cell proliferation, survival, and metastasis. By encapsulating the BG129 peptide within a nanoliposome, the formulation enhances the peptide's stability, protects it from proteolytic degradation, and extends its circulatory half-life. This delivery system also facilitates improved accumulation of the therapeutic peptide at the tumor site through the enhanced permeability and retention (EPR) effect. Developed by Nanolipo, nLs-BG129 has demonstrated significant anti-tumor activity in preclinical models and is currently undergoing evaluation in Phase 1 clinical trials to determine its safety, tolerability, and preliminary efficacy in patients with advanced pancreatic cancer.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on nLs-BG129.