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Abraxis receives European marketing approval for Abraxane(R) PDF Print E-mail
News - Nanomedicine and Drug Delivery News Archive
Tuesday, 22 January 2008
Abraxis BioScience announced that the European Medicines Agency (EMEA) granted marketing approval for Abraxane(R) (paclitaxel protein-bound particles for injectable suspension) for the treatment of metastatic breast cancer in patients who have failed first-line treatment.

 

Abraxane(R) is a proprietary nanoparticle formulation that entraps paclitaxel into particles comprised of an albumin shell. This formulation has been developed using Abraxis' nab(TM) technology. This technology takes advantage of a specialized protein called SPARC (Secreted Protein Acidic and Rich in Cysteine) into the tumor's interstitium that acts as a highly charged receptor to specifically attract and bind albumin. The SPARC protein function is to concentrate albumin-bound nutrients within the tumor's interstitium to prevent nutrients from diffusing outside the tumor cell.

Abraxis expects to launch Abraxane(R) in European countries in mid-2008. Abraxane(R) is already approved in US and Canada.

Source: Abraxis BioScience, Inc.

 
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