UH3DA048379
Cooperative Agreement
Overview
Grant Description
Arylepoxamides: A New Class of Potent, Safer Analgesics
The expansion of opioid prescribing in recent years to better treat pain has markedly increased their usage and availability, fueling an epidemic of abuse. Estimates suggest that up to 80% of addicts reported initiating their habit through prescription drugs. Decreasing opioid prescriptions would lower opioid exposure, with fewer people receiving the drugs and less drug available for diversion.
We have identified a novel target in the brain, distinct from any of the traditional opioid receptors, capable of mediating potent analgesia without the reward behavior and side-effects seen with traditional opioids. We have targeted this site with a series of arylepoxamides and have identified a clinical candidate (MP1000) and backup compound.
MP1000 is a potent analgesic in a range of thermal, inflammatory, and neuropathic analgesic assays. It fails to show reward behavior and does not produce respiratory depression at doses 5-fold greater than its analgesic ED50. Chronic administration does not produce physical dependence or withdrawal when challenged with an antagonist. It shows no cross-tolerance to morphine and can be co-administered to subjects already on opioids for pain to lower their opioid usage (i.e., 'opioid sparing'), facilitating the eventual discontinuation of the opioid.
Preliminary safety and toxicology studies are encouraging, and based upon these results, we are proposing to carry out IND-enabling studies and a Phase 1 clinical trial.
The expansion of opioid prescribing in recent years to better treat pain has markedly increased their usage and availability, fueling an epidemic of abuse. Estimates suggest that up to 80% of addicts reported initiating their habit through prescription drugs. Decreasing opioid prescriptions would lower opioid exposure, with fewer people receiving the drugs and less drug available for diversion.
We have identified a novel target in the brain, distinct from any of the traditional opioid receptors, capable of mediating potent analgesia without the reward behavior and side-effects seen with traditional opioids. We have targeted this site with a series of arylepoxamides and have identified a clinical candidate (MP1000) and backup compound.
MP1000 is a potent analgesic in a range of thermal, inflammatory, and neuropathic analgesic assays. It fails to show reward behavior and does not produce respiratory depression at doses 5-fold greater than its analgesic ED50. Chronic administration does not produce physical dependence or withdrawal when challenged with an antagonist. It shows no cross-tolerance to morphine and can be co-administered to subjects already on opioids for pain to lower their opioid usage (i.e., 'opioid sparing'), facilitating the eventual discontinuation of the opioid.
Preliminary safety and toxicology studies are encouraging, and based upon these results, we are proposing to carry out IND-enabling studies and a Phase 1 clinical trial.
Awardee
Funding Goals
TO SUPPORT BASIC AND CLINICAL NEUROSCIENCE, BIOMEDICAL, BEHAVIORAL AND SOCIAL SCIENCE, EPIDEMIOLOGIC, HEALTH SERVICES AND HEALTH DISPARITY RESEARCH. TO DEVELOP NEW KNOWLEDGE AND APPROACHES RELATED TO THE PREVENTION, DIAGNOSIS, TREATMENT, ETIOLOGY, AND CONSEQUENCES OF DRUG ABUSE AND ADDICTION, INCLUDING HIV/AIDS. TO SUPPORT RESEARCH TRAINING AND RESEARCH SCIENTIST DEVELOPMENT. TO SUPPORT DISSEMINATION OF RESEARCH FINDINGS. SMALL BUSINESS INNOVATION RESEARCH (SBIR) LEGISLATION IS INTENDED TO EXPAND AND IMPROVE THE SBIR PROGRAMS TO EMPHASIZE AND INCREASE PRIVATE SECTOR COMMERCIALIZATION OF TECHNOLOGY DEVELOPED THROUGH FEDERAL SBIR RESEARCH AND DEVELOPMENT, INCREASE SMALL BUSINESS PARTICIPATION IN FEDERAL RESEARCH AND DEVELOPMENT, AND FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN THE SBIR PROGRAM. THE LEGISLATION INTENDS THAT THE SMALL BUSINESS TECHNOLOGY TRANSFER (STTR) PROGRAM STIMULATE AND FOSTER SCIENTIFIC AND TECHNOLOGICAL INNOVATION THROUGH COOPERATIVE RESEARCH AND DEVELOPMENT CARRIED OUT BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, FOSTER TECHNOLOGY TRANSFER BETWEEN SMALL BUSINESS CONCERNS AND RESEARCH INSTITUTIONS, TO INCREASE PRIVATE SECTOR COMMERCIALIZATION OF INNOVATIONS DERIVED FROM FEDERAL RESEARCH AND DEVELOPMENT, AND FOSTER AND ENCOURAGE PARTICIPATION OF SOCIALLY AND ECONOMICALLY DISADVANTAGED SMALL BUSINESS CONCERNS AND WOMEN-OWNED SMALL BUSINESS CONCERNS IN TECHNOLOGICAL INNOVATION.
Grant Program (CFDA)
Awarding / Funding Agency
Place of Performance
New York
United States
Geographic Scope
State-Wide
Related Opportunity
Analysis Notes
Amendment Since initial award the End Date has been extended from 08/31/24 to 08/31/26 and the total obligations have increased 199% from $4,595,217 to $13,729,308.
Sparian Biosciences was awarded
Arylepoxamides: A new class of potent, safer analgesics
Cooperative Agreement UH3DA048379
worth $13,729,308
from National Institute on Drug Abuse in December 2018 with work to be completed primarily in New York United States.
The grant
has a duration of 7 years 8 months and
was awarded through assistance program 93.279 Drug Abuse and Addiction Research Programs.
The Cooperative Agreement was awarded through grant opportunity Development of Medications to Prevent and Treat Opioid Use Disorders and Overdose (UG3/UH3) (Clinical Trials Optional).
Status
(Ongoing)
Last Modified 9/24/25
Period of Performance
12/15/18
Start Date
8/31/26
End Date
Funding Split
$13.7M
Federal Obligation
$0.0
Non-Federal Obligation
$13.7M
Total Obligated
Activity Timeline
Transaction History
Modifications to UH3DA048379
Additional Detail
Award ID FAIN
UH3DA048379
SAI Number
UH3DA048379-2187664754
Award ID URI
SAI UNAVAILABLE
Awardee Classifications
Small Business
Awarding Office
75N600 NIH National Insitute on Drug Abuse
Funding Office
75N600 NIH National Insitute on Drug Abuse
Awardee UEI
E6GKXJ7MWV68
Awardee CAGE
8EU60
Performance District
NY-90
Senators
Kirsten Gillibrand
Charles Schumer
Charles Schumer
Budget Funding
Federal Account | Budget Subfunction | Object Class | Total | Percentage |
---|---|---|---|---|
National Institute on Drug Abuse, National Institutes of Health, Health and Human Services (075-0893) | Health research and training | Grants, subsidies, and contributions (41.0) | $9,134,091 | 100% |
Modified: 9/24/25