SBIR/STTR Research Award

Somatostatin Mimetics as Novel Anti-Epileptic Drugs

Award identifier eb8a77f6f2c1163b56b1be9582cb9425163f3054bf36f2c4e8125ba9d0ec4558Awarding agency Department of Health and Human Services · National Institutes of Health

Award amount

$101,352

Program and phase

STTR · Phase I

Award year

2003

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Award details

Awarding agency
Department of Health and Human Services
Branch
National Institutes of Health
Recipient company
RFE PHARMA, 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): The epilepsies are a family of neurological disorders characterized by seizures which are transient, recurrent perturbations of normal brain function. As a chronic condition, epilepsy affects about 1 percent of the population in the United States. While anti-epileptic drug (AED) treatment is the standard therapy for epilepsy, one third of all patients remain unresponsive to currently available medications. A growing body of research indicates that controlling seizure activity is an important physiological function for somatostatin in the CNS. Therefore, centrally active somatostatin analogs have potential to be novel, effective AEDs with a well defined molecular mechanism of action. A new structural class of potent non-peptide somatostatin mimetics with demonstrated CNS activity provides the starting point of the plan. This class of compounds will be optimized for in vitro potency and lipophilicity. Potential CNS drugs selected based on these in vitro parameters will be screened in vivo for efficacy in the acute seizure, rat kindling model of epilepsy. The rat chronic limbic epilepsy model will be used (largely in Phase II) to screen for compounds that are also active against spontaneous seizures and therefore have the greatest potential for demonstrating clinical efficacy in man.

Technology keywords

Not reported

Agency intelligence

Department of Health and Human Services

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