The USA's SD Pharmaceuticals says it has completed a battery of preclinical studies on SDP-013, its novel nano-emulsion formulation of the cancer drug paclitaxel, which showed equal or superior efficacy in a mouse model of human ovarian cancer (SK-OV-3 cell line), a "very favorable" toxicity profile and a lack of immunogenicity compared to the existing branded formulation of the drug, sold by US health care major Bristol-Myers Squibb as Taxol.
The firm concluded that SDP-013 is equivalent to Taxol and free of the immunogenicity associated with it and other paclitaxel formulations. The agent also showed dose-dependant efficacy in a mouse model, as judged by reduction in tumor burden, that were equal to or slightly better than Taxol with similar, if not superior, side effect profiles. The comapany added that the immunosensitivity study showed no sensitization, which it describes as a "major problem" with the currently-marketed Taxol formulation.
This article is accessible to registered users, to continue reading please register for free. A free trial will give you access to exclusive features, interviews, round-ups and commentary from the sharpest minds in the pharmaceutical and biotechnology space for a week. If you are already a registered user please login. If your trial has come to an end, you can subscribe here.
Login to your accountTry before you buy
7 day trial access
Become a subscriber
Or £77 per month
The Pharma Letter is an extremely useful and valuable Life Sciences service that brings together a daily update on performance people and products. It’s part of the key information for keeping me informed
Chairman, Sanofi Aventis UK
Copyright © The Pharma Letter 2025 | Headless Content Management with Blaze