SBIR-STTR Award

Transdermal Delivery of Tetrahydro-Cannabinol
Award last edited on: 1/30/14

Sponsored Program
SBIR
Awarding Agency
NIH : NIDA
Total Award Amount
$462,693
Award Phase
2
Solicitation Topic Code
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Principal Investigator
Ram Murty

Company Information

Murty Pharmaceuticals Inc

518 Codell Drive
Lexington, KY 40509
   (859) 266-2446
   info@mpirx.com
   www.mpirx.com
Location: Single
Congr. District: 06
County: Fayette

Phase I

Contract Number: N43DA007705-000
Start Date: 00/00/00    Completed: 00/00/00
Phase I year
2000
Phase I Amount
$99,683
Dronabinol is effective as an anti-emetic in anorexia, and for treating nausea and frequent vomiting in cancer chemotherapy. This is currently administered orally, and is not always effective. A meta-analysis study revealed a poor or partial response to dronabinol in approximately 65% of 750 courses of oral therapy. Thus high single doses of this drug are administered causing side effects such as sedation, confusion, and anxiety. These problems could be minimized by the administration of sustained low doses of dronabinol via a trans-dermal patch. This route of administration will reduce the variation in absorption and metabolism, associated with oral administration and on the other hand increase the bio-availability and the efficacy by avoiding liver first-pass inactivation. Therapeutics plasma levels of dronabinol will be estimated from in vitro diffusion experiments and drug distribution between immiscible solvents. During this phase I SBIR project, the contractor proposes to develop the dronabinol dermal adhesive patch for safer delivery of drug to the system.

Phase II

Contract Number: N44DA017705-001
Start Date: 00/00/00    Completed: 00/00/00
Phase II year
2002
Phase II Amount
$363,010
___(NOTE: Note: no official Abstract exists of this Phase II projects. Abstract is modified by idi from relevant Phase I data. The specific Phase II work statement and objectives may differ)___ Dronabinol is effective as an anti-emetic in anorexia, and for treating nausea and frequent vomiting in cancer chemotherapy. This is currently administered orally, and is not always effective. A meta-analysis study revealed a poor or partial response to dronabinol in approximately 65% of 750 courses of oral therapy. Thus high single doses of this drug are administered causing side effects such as sedation, confusion, and anxiety. These problems could be minimized by the administration of sustained low doses of dronabinol via a trans-dermal patch. This route of administration will reduce the variation in absorption and metabolism, associated with oral administration and on the other hand increase the bio-availability and the efficacy by avoiding liver first-pass inactivation. Therapeutics plasma levels of dronabinol will be estimated from in vitro diffusion experiments and drug distribution between immiscible solvents. During this phase I SBIR project, the contractor proposes to develop the dronabinol dermal adhesive patch for safer delivery of drug to the system.