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.
Therapeutic antibodies have shown immense success in the marketplace
and drug development pipelines are increasingly dominated by them.
However, due to the requirement of a high therapeutic dose antibodies
are often administered by slow intravenous infusions taking several
hours and necessitating the involvement of local hospitals. This is
not only inconvenient for patients but localizes administration to
clinical settings which can be costly.
A number of big pharmaceutical and biotechnology companies are
presently seeking novel ways of increasing the therapeutic dose for
their proprietary antibodies to levels as high as 50-200 mg/ml.
Through the application of Arestat™ technologies, Arecor has
demonstrated that higher concentrations of proteins can be maintained
in storage without degradation or aggregation typically associated with
such formulations. Arecor is working with a range of approved recombinant
therapeutic proteins at significantly higher doses than the marketed
brands thereby creating opportunities for new routes of administration
for these formulations.