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Peripheral FAAH as a target for novel analgesics

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 2R42DA033683-02A1
Agency Tracking Number: R42DA033683
Amount: $1,498,471.00
Phase: Phase II
Program: STTR
Solicitation Topic Code: NIDA
Solicitation Number: PA14-072
Timeline
Solicitation Year: 2014
Award Year: 2017
Award Start Date (Proposal Award Date): 2017-03-15
Award End Date (Contract End Date): 2020-11-30
Small Business Information
10575 ROSELLE ST
San Diego, CA 92121-1505
United States
DUNS: 078765734
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 DANIELE PIOMELLI
 (949) 824-6180
 piomelli@uci.edu
Business Contact
 MIGUEL GARCIAGUZMAN
Phone: (858) 205-5904
Email: mgguzman@me.com
Research Institution
 UNIVERSITY OF CALIFORNIA-IRVINE
 
141 INNOVATION DRIVE, SUITE 250
IRVINE, CA 92617-3213
United States

 Nonprofit College or University
Abstract

DESCRIPTIONprovided by applicantPain management is a significant unmet medical needAnandamide is an endocannabinoid mediator that plays important roles in the regulation of painPrevious work has shown that endocannabinoid receptors located outside the central nervous systemCNSexert a powerful regulatory control over pain initiationThe biological actions of anandamide are stopped by the enzymefatty acid amide hydrolaseFAAHTo explore the role of anandamide in the peripheral regulation of painour lab has developed a novel class of FAAH inhibitors that do not enter the CNSThe lead compound in this classcalled URBexerts profound analgesic effects in animal modelssuggesting that peripheral FAAH blockade may offer an innovative approach to pain therapyWork done during the Phaseof the present application has demonstrated that URBasuppresses postoperative pain in mice more effectively than do currently used analgesicsbdoes not cause side effects typical of those drugsi esedationconstipationgastric damagecshows a high degree of target selectivitydhas excellent oral bioavailability in ratsandeexerts no genotoxic effcts in the Amesandapostest and does not inhibit the human potassium hERG channelThese results identify URBas a suitable candidate for preclinical development in postoperative painan extremely common but still underserved pain conditionThe objective of present proposal is to complete all key activities needed to enable the filing of an Investigational New DrugINDfor URBin postoperative painOur specific aims areAimSynthesis and physicochemical characterization of URBWe will produce a large scale lot of URBfor use in nonclinical pharmacokinetics and toxicology studiesAimDrug metabolismDMand pharmacokineticPKproperties of URBWe will collect the DM PK data necessary to support the IND filing of URBAimNonclinical toxicology properties of URBWe will collect the toxicology data necessary to support the IND filing of URBAimNonclinical pharmacodynamics of URBWe will develop a circulating biomarker for peripheral FAAH inhibitionwhich will be of great value during the clinical development of URBThe proposed studies will be coordinated by an experienced team of scientists and pharmaceutical professionalswhich include Anteanaandapos s cofoundersProfessor Daniele Piomelli and DrMiguel Garcia GuzmanProfessor Andrew RiceImperial CollegeLondona world recognized leader in pain therapyalong with and independent consultants DrEdward MonaghanSoar Pharmaceutical Development Servicespreclinical developmentDrFred RenotoxicologyDrWilliam SchmidtNorthStar Consultinghealth economicsDrJason BrittainJNG Pharmaceutical ConsultingChemistryManufacturingand Controlsand DrRichard LowenthalPacific Link Consultingregulatory affairsWe expect that the successful completion of our studies will provide the data needed to file an IND for URBand allow us to raise the private capital necessary to bring this compound to clinical proof of conceptPUBLIC HEALTH RELEVANCECurrent painkillers work well in only about one quarter of the patients who take themand can cause a variety of negative effectsfor examplesedation and addictionby acting on cells of the brainOur lab has recently discovered a new class of medicationscalled `peripheral FAAH inhibitorsandaposwhich cannot enter the brain yet produce powerful pain suppression in experimental modelsHerewe propose a series of studies that will enable the clinical testing of the lead compound in this class for the treatment of acute pain after surgery

* Information listed above is at the time of submission. *

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