Cooperative Agreement UG3DA058553
- Federal Cooperative Agreement Summary Yale University, in collaboration with the University of California, Los Angeles (UCLA), received a $1.64 million Cooperative Agreement from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279) awarded on July 15, 2025, with completion by June 30, 2027. The award supports the development and validation of the Stimulant Use Disorder Severity Scale (STUDSS) as a Food and Drug Administration (FDA)-qualified...
- The University of Texas Southwestern Medical Center received a $1.32 million Project Grant from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279), awarded August 15, 2025, with completion targeted for July 31, 2027. The RESTORE (Recovery and Engagement for Stimulant Users on Re-entry) Study will develop and pilot-test an integrated intervention combining contingency management (CM) delivered via the FDA-approved DynamiCare mobile application...
- Federal Grant Award Summary The National Institute on Drug Abuse (NIDA) awarded a $2.09 million Project Grant (R01 Stage IIA mechanism) to the University of Texas Health Science Center at Houston on June 15, 2025, under the Drug Use and Addiction Research Programs (CFDA 93.279) to conduct a pilot mechanistic study investigating semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA), as a pharmacological treatment for cocaine use disorder (CUD). The research addresses a critical public...
- Federal Cooperative Agreement Award Summary The National Institute on Drug Abuse (NIDA) awarded $2,040,300 to the Regents of the University of Minnesota on September 1, 2025, under the Drug Use and Addiction Research Programs (CFDA 93.279) to develop and evaluate a combined transcranial direct current stimulation (tDCS) and cognitive training intervention as an adjunctive treatment for opioid use disorder (OUD). The research addresses a critical clinical gap: despite widespread buprenorphine...
- Federal Cooperative Agreement Award Summary Public Health Foundation Enterprises, Inc. (doing business as Heluna Health) received a $1.94M Cooperative Agreement from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279) to conduct a two-phase clinical research study investigating semaglutide, a glucagon-like peptide-1 (GLP-1) agonist, as a treatment for methamphetamine use disorder (MEUD). The award, effective September 1, 2025, through August...
- Federal Grant Award Summary The National Institute on Drug Abuse (NIDA) awarded Massachusetts General Hospital $395,280 under the Drug Use and Addiction Research Programs (CFDA 93.279) to develop and evaluate AMP-C, a digital therapeutic (DTX) intervention targeting reward dysfunction in individuals with co-occurring Cannabis Use Disorder (CUD) and Major Depressive Disorder (MDD). This five-year project grant, effective July 1, 2025 through June 30, 2030, delivers a user-centered digital...
- Federal Cooperative Agreement Summary The National Institute on Drug Abuse (NIDA) awarded a $1.37 million Cooperative Agreement to New York University School of Medicine, effective July 15, 2025, under the Drug Use and Addiction Research Programs (CFDA 93.279) to develop and test a telehealth-delivered transcranial direct current stimulation (tDCS) intervention for cannabis use disorder (CUD). The C.A.R.E.S. (Cannabis Addiction Recovery Enhancement Stimulation) Initiative combines home-based...
- Syncanica Bio, Inc. received a Project Grant of $334,343 from the National Institute on Drug Abuse (NIDA) under the Drug Use and Addiction Research Programs (CFDA 93.279), awarded June 15, 2025, with completion targeted for May 31, 2027. The company is developing fully synthetic analogs of 8,9-dihydrocannabidiol (H2CBD) as therapeutic agents to treat substance use disorder (SUD), a public health crisis with limited treatment options. This research builds on preliminary evidence indicating that...
- This $2.11 million Project Grant awarded by the National Institute on Drug Abuse (NIDA) under the Drug Use and Addiction Research Programs (CFDA 93.279) supports research conducted by Pennsylvania State University's Milton S. Hershey Medical Center from May 2025 through February 2030. The award funds investigational research on cocaine addiction using an animal model to identify individual vulnerability to addiction early in disease development and to test early intervention strategies. The...
- This federal Project Grant award from the National Institute on Drug Abuse (NIDA), under the Drug Use and Addiction Research Programs (CFDA 93.279), provides $419,876 to conduct preclinical trials targeting the neuropeptide S (NPS) receptor to mitigate opioid taking and seeking behaviors in animal models. The goals of the project are to demonstrate proof-of-concept that NPS receptor-targeted molecules can reduce oxycodone self-administration and motivation in rats, which could inform the...
DEVELOPMENT OF SIGMA RECEPTOR/DAT DUAL-TARGETING COMPOUNDS TO TREAT STIMULANT USE DISORDER - ABSTRACT THE GROWING PREVALENCE OF STIMULANT USE DISORDER (STUD) IN THE US IS A MAJOR PUBLIC HEALTH CONCERN. AS OF 2020, 3.2M PEOPLE HAD STUD IN THE US, WHICH EXCEEDS THE 2.7M PEOPLE WITH OPIOID USE DISORDER (OUD), AND THERE WERE ~57K STIMULANT-RELATED OVERDOSE DEATHS IN 2021. IN FACT, STIMULANTS ARE CONSIDERED THE "4TH WAVE" OF THE OVERDOSE CRISIS. IN 2020, NIDA DIRECTOR NORA VOLKOW, MD STATED THAT "ALTHOUGH DEATHS FROM OPIOIDS CONTINUE TO COMMAND THE PUBLIC'S ATTENTION, AN ALARMING INCREASE IN DEATHS INVOLVING THE STIMULANT DRUGS METHAMPHETAMINE AND COCAINE ARE A STARK ILLUSTRATION THAT WE NO LONGER FACE JUST AN OPIOID CRISIS". DESPITE SUBSTANTIAL R & D EFFORTS, THERE IS NO FDA-APPROVED PHARMACOTHERAPY FOR THE TREATMENT OF STUD - IN CONTRAST TO OUD WHERE MEDICATION-ASSISTED TREATMENT (MAT) IS THE STANDARD OF CARE - AND THERE IS AN URGENT NEED FOR SUCH. THIS UG3/UH3 PROPOSAL AIMS TO DEVELOP SBS-518 AS A FIRST-IN-CLASS TREATMENT FOR STUD. SBS- 518 IS A DUAL SIGMA RECEPTOR ANTAGONIST AND DOPAMINE ACTIVE TRANSPORT (DAT) INHIBITOR. WE HAVE DEMONSTRATED THAT SBS-518 DECREASES STIMULANT SELF-ADMINISTRATION IN RATS, WITHOUT BEING REWARDING ITSELF. THESE DATA SUPPORT THE DEVELOPMENT OF SBS-518 AS A NOVEL, FIRST-IN-CLASS TREATMENT FOR STUD. IN THE UG3, WE WILL CONDUCT A TARGETED LEAD OPTIMIZATION TO SELECT OUR LEAD COMPOUND (SBS- 518X) AND QUICKLY MOVE INTO DEVELOPMENT. WE WILL CONDUCT NONGMP API AND DRUG PRODUCT DEVELOPMENT, NONGLP TOXICOLOGY STUDIES, AND SUBMIT FOR A PRE-IND MEETING WITH FDA TO ALIGN ON THE IND-ENABLING PROGRAM. BY THE END OF THE UG3, WE WILL HAVE OUR IDENTIFIED OUR CLINICAL CANDIDATE AND CONDUCTED PRELIMINARY CMC AND TOX WORK. IN THE UH3, WE WILL CONDUCT THE IND- ENABLING CMC AND TOXICOLOGY WORK, SUBMIT AN IND AND CONDUCT A PHASE 1 CLINICAL TRIAL. IN SUMMARY, WE PROPOSE TO DEVELOP A NOVEL AGENT FOR STUD AND BRING IT THROUGH A FIRST IN HUMAN CLINICAL TRIAL.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $0 | 3/18/26 | ||
| Not listed | $0 | 5/22/25 | ||
| Not listed | $0 | 11/29/24 | ||
| Not listed | $0 | 11/29/24 | ||
| Not listed | $0 | 11/29/24 |
GrantNumber | Description | Subgrantee | Prime Award | Dollars Obligated | Updated At |
|---|---|---|---|---|---|
SBS518UG3UFY2S | University Of Florida | Cooperative Agreement UG3DA058553 | $483.8k | 9/9/24 |