SBIR/STTR Research Award
CRF-TYPE-2 RECEPTOR ANTAGONISTS FOR ANXIETY
Award amount
$133,540Program and phase
SBIR · Phase IAward year
2002Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- Neurocrine Biosciences, Inc.
- Proposal award date
- Not reported
- Contract end date
- Not reported
- UEI
- Not reported
- Solicitation number
- Not reported
- Topic code
- Not reported
Research abstract
DESCRIPTION (provided by applicant): Since the CRF2 receptor was cloned in
1995, relatively little has been learned about its functional biology due
primarily to the lack of pharmacological tools. Anatomical distribution data
had suggested that the CRF2 receptor could be involved in feeding behaviors,
which led to the idea that an antagonist to this receptor could have utility in
treating eating disorders like anorexia nervosa. Recently, however, a selective
peptide antagonist (antisauvagine-30) and agonist (urocortin II) have become
available. Preliminary data obtained with antisauvagine-30 and urocortin II
verified the importance of the CRF2 receptor in anorectic behavior, but the
antisauvagine-30 (ASV-30) data also suggested that the CRF2 receptor may be
involved in emotional behavior and anxiety. Thus, the potential therapeutic
market for a CRF2 receptor antagonist could include a much broader spectrum of
emotional disorders than anorexia nervosa. Therefore, we have proposed to
investigate the possibility that the CRF2 receptor plays a role in anxious
behavior, using ASV-30 and urocortin II as pharmacological tools. In
anticipation of a positive finding, we have also proposed to begin the process
of identifying a selective, high affinity, orally available CRF2 antagonist
that could be used not only for the treatment of anorexia nervosa, but also for
the treatment of anxiety disorders. Therefore, Phase I is focused: 1) on
biological proof of principle for the role of CRF2 receptors in anxiety, and 2)
on the initial identification of a high affinity CRF2 antagonist. Phase II
would follow up with the actual development of such an antagonist, fine-tuning
for selectivity, oral bioavailability and safety.
PROPOSED COMMERCIAL APPLICATION:
A small molecule CRF2 receptor antagonist could represent an anti?anxiety therapeutic with a novel mechanism of action and the potential to provide an improved efficacy and side effect profile in comparison to available therapeutics. Anxiety disorders are the most common form of mental illness in the United States, with an estimated one year prevalence of 16.4%, and an estimated cost of $993/year/person (USDHHS, et al., 1999).
Technology keywords
Not reported