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Identification of Mixed NOP/mu partial agonists as lead compounds for treatment ofmethamphetamine use disorder

Award Information
Agency: Department of Health and Human Services
Branch: National Institutes of Health
Contract: 1R41DA057430-01
Agency Tracking Number: R41DA057430
Amount: $319,983.00
Phase: Phase I
Program: STTR
Solicitation Topic Code: NIDA
Solicitation Number: DA22-018
Timeline
Solicitation Year: 2022
Award Year: 2023
Award Start Date (Proposal Award Date): 2023-05-15
Award End Date (Contract End Date): 2024-05-14
Small Business Information
999 West 1500 South #600
Woodscross, UT 84087
United States
DUNS: 193291403
HUBZone Owned: No
Woman Owned: No
Socially and Economically Disadvantaged: No
Principal Investigator
 ANDREA CIPPITELLI
 (561) 297-4288
 acippitelli@health.fau.edu
Business Contact
 WILLIAM CROSSMAN
Phone: (860) 305-6955
Email: bill@phoenixpharmalabs.com
Research Institution
 FLORIDA ATLANTIC UNIVERSITY
 
777 GLADES ROAD
BOCA RATON, FL 33431-6424
United States

 Nonprofit College or University
Abstract

Abstract
Currently, clinically used drug abuse medications exist for treatment of addiction to opiates, alcohol, and nicotine,
but not psychostimulants, such as methamphetamine (METH). Compounds that co-activate both nociceptin
opioid peptide (NOP) and mu receptors have potential for treatment of drug abuse. In particular, buprenorphine,
a partial mu agonist/kappa antagonist, which also acts as a low affinity and partial agonist at NOP, is used as an
opioid use disorder medication and has demonstrated analgesic properties and efficacy in reducing cocaine and
alcohol consumption, reportedly through its efficacy at NOP receptors. As NOP receptor activation reduces
reward induced by mu activation, new molecules with bifunctional mu/NOP activities were designed to develop
compounds with reduced abuse liability and increased efficacy as potential treatment for substance use disorder
as compared to buprenorphine. Among a family of structurally related mixed compounds, Phoenix PharmaLabs
has licensed a series of compounds with bifunctional NOP/mu activity. Two ligands, PPL-138 and PPL-143, were
shown to have the highest NOP receptor affinity and potency, with PPL-143 showing the greatest efficacy for
NOP. Like buprenorphine, the two compounds have high affinity and low efficacy at mu receptors and high affinity
and antagonist activity at kappa receptors. NOP receptor agonists have previously been demonstrated to block
METH conditioned place preference. Recently, we found that PPL-138 successfully decreases METH self-
administration in rats. In this application, we propose animal studies to examine the safety and the efficacy of
PPL-138 and PPL-143 as candidate medications for METH use disorder (MUD) and to choose a lead compound
for further development. Specific Aim 1 will assess the efficacy of both compounds in reducing METH-taking
behavior and motivation for METH in animals exposed to long METH access, a procedure that closely reflects
the compulsive nature of MUD. As relapse is a central feature of MUD, the two compounds will also be evaluated
for their ability to reduce reinstatement of METH-seeking behavior. These experiments will be conducted both in
male and female rats. Specific Aim 2 will determine safety of PPL-138 and PPL-143 by evaluating their
reinforcing properties and possible tolerance development. Concurrently to the first two aims, Specific Aim 3
will conduct preliminary pharmacokinetic and ADME studies on PPL-143, which will integrate the behavioral
results. Collectively, the experiments planned in the present proposal will determine whether increasing the NOP
component in the context of a mu/NOP co-activation has any advantages over buprenorphine in terms of efficacy
and safety. These experiments will also inform on further development of the mixed ligands as potential MUD
pharmacotherapies, choose a lead compound for further development, and provide an important contribution to
the literature of the NOP system and the METH addiction fields.

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

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