Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
RRWQWR-Ahx-RWQWRWQWR is a synthetic, cationic hybrid peptide designed for the treatment of cervical cancer. It is constructed using a hybrid peptide formation strategy that combines two fragments derived from bovine lactoferricin (LfcinB): the hexapeptide RRWQWR and the palindromic nonapeptide RWQWRWQWR, joined by a 6-aminohexanoic acid (Ahx) spacer. The peptide's mechanism of action is based on its amphipathic nature; the arginine residues facilitate an initial electrostatic interaction with the negatively charged components of the cancer cell surface, while the tryptophan residues subsequently interact with and disrupt the lipid bilayer of the cell membrane, potentially leading to internalization and apoptosis. Developed by researchers in Colombia, this peptide has demonstrated significant, rapid, and selective in vitro cytotoxic activity against human cervical cancer cell lines HeLa and Ca Ski, while showing lower toxicity toward healthy fibroblasts and red blood cells.
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 RRWQWR-Ahx-RWQWRWQWR.