SBIR/STTR Research Award
Preformulation and formulation development of Fenrock an Abuse resistant Fentanyl Transdermal Patch
Award amount
$349,947Program and phase
SBIR · Phase IAward year
2017Award details
- Awarding agency
- Department of Health and Human Services
- Branch
- National Institutes of Health
- Recipient company
- PAIN THERAPEUTICS, INC.
- Proposal award date
- 2017-09-01
- Contract end date
- 2019-05-31
- UEI
- Not reported
- Solicitation number
- PA16-302
- Topic code
- NIDA
Research abstract
Project Summary Abstract
Under this Fast Track proposal we will develop FenrockTM an abuse deterrent transdermal
fentanyl patch based on our proprietary co crystal of naltrexone NTX and its carefully selected
conformer methyl furfural MFF This NTX MFF co crystal NTX Co has the desired
properties to stay in a crystalline solid form in the patch when applied to skin as intended but to
dissociate to deliver NTX when abused by chewing swallowing solvent extraction smoking or
heating and inhaling We will first develop analytical methods needed to measure the three patch
components fentanyl NTX and MFF We will perform preformulation studies to assess solid
state interaction of NTX Co with fentanyl and various excipients as well as compatibility with
various pressure sensitive adhesives The stability of NTX Co in the presence of fentanyl and the
list of acceptable excipients and adhesives will determine potential compartmental designs We
will then begin formulation development by testing several potential fentanyl and NTX Co patch
components compartments and characterizing them individually in in vitro in dissolution and flux
across an artificial membrane under use and abuse simulations These results and adhesion
testing will determine the Phase I milestone selection of up to three patch prototype concepts
with integrated fentanyl and NTX Co compartments Phase II of this proposal will begin with
production of these three patch prototype designs and their in vitro testing under use and abuse
paradigms These include D tissue models of transdermal and buccal absorption and in vitro
tests to mimic chewing swallowing solvent extraction and volatilization by heating or smoking A
final ex vitro test will assess transdermal absorption in excised human skin Up to two patch
prototypes will be selected for a PK study in rats to compare fentanyl absorption rate to that of
the Duragesic fentanyl patch Based on these data one or two prototypes will be selected for a
dermal irritation study in rats and a PK study in minipig that will guide the IND enabling studies in
minipig the required species for transdermal products We will use the rat conditioned place
preference paradigm to determine the optimal relative doses of NTX Co and fentanyl such that
enough NTX is released under scenarios of abuse to reduce the rewarding effects of fentanyl and
provide a measure of safety With the PK dermal irritation and relative dose determination
completed one formulation will be selected and a GLP tox lot manufactured We will then conduct
a dose range finding study and the pivotal day GLP tox in minipig At the completion of the
proposed work Fenrock will be ready for GMP scale up and clinical trials Project Narrative
Abuse and accidental misuse of transdermal fentanyl patches is a serious health issue when
exposed to liquids or put in the mouth a day supply of this fast acting and highly potent opiate
is delivered quickly We proposed to develop FenrockTM an abuse deterrent transdermal fentanyl
patch based on our proprietary co crystal of naltrexone The co crystal will remain in the patch
undelivered when applied as intended but will release naltrexone to counteract the fentanyl if the
patch is abused by chewing swallowing solvent extraction smoking or heating and inhaling
Technology keywords
Not reported
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