Arestat™ Protein Stabilisation Technology
Arestat™ comprises two fundamentally different aspects of our platform stabilisation technology – Arestat-T™ and Arestat-R™. Both utilise excipients and buffers approved by the FDA and EMEA in an unconventional manner to achieve the desired stability.
Both are available for licensing for therapeutic proteins, vaccines, medial devices and diagnostics.
Welcome to Arecor
Arecor has developed Arestat™, a formulation technology, which enables the formulation of labile proteins and vaccines as stable aqueous formulations even at high concentrations or in the presence of ionising radiation.
As a simple reformulation, the technology can be readily integrated into existing manufacturing processes. Arestat™ does not involve the covalent modification of biologics and uses only GRAS (Generally Regarded As Safe) excipients approved by relevant regulatory authorities.
Arecor is collaborating with a number of pharmaceutical and biotech companies to develop recombinant proteins and vaccines for application in drugs, medical devices or diagnostics.
Arestat™ has a proven track record and has been incorporated into a Class III medical device (Oxyzyme™) approved in the EU and Canada. It is currently being applied to several recombinant biologics in various stages of development for administration via parenteral, ocular and transdermal routes.