Arestat™ comprises two fundamentally different aspects of
our platform stabilization technology. Both utilize excipients
and buffers approved by the FDA and EMEA in an unconventional
manner to achieve the desired stability.
Both platform technologies are available for licensing for applications involving
therapeutic proteins, vaccines, medical devices and diagnostics.
There are many biologics in the development pipeline for whom
stability during manufacture and in storage are significant
issues. Recombinant proteins, single chain antibodies, fusion
proteins, nucleic acids and vaccines are often plagued with the
challenge of overcoming unwanted instabilities. Consequently
some promising therapeutic candidates never make it beyond early
development phase for want of a stable formulation acceptable to
the pharmaceutical industry.
Arecor has demonstrated that biologics considered difficult to
formulate can be progressed as development candidates through
the application of Arestat™ technologies. One such case
involved a single chain antibody showing therapeutic promise but
an unacceptable stability profile. Through the application of
Arestat-T™ technology Arecor has been able to overcome
the instability allowing the product to be considered as a
clinical candidate.