Project Grant R43DA056084
- Federal Project Grant Award Summary Verisim Life, Inc. received a $1.48M Phase II Project Grant award from the National Institute on Drug Abuse (NIDA) under the Drug Use and Addiction Research Programs (CFDA 93.279) effective July 15, 2025, with a completion date of July 31, 2028. The company will develop novel therapeutic candidates for stimulant use disorder (STUD) leveraging its proprietary BioSim artificial intelligence (AI)-driven drug discovery platform. Specifically, Verisim Life will...
- Federal Grant Award Summary Callentis Consulting Group LLC received a $795,658 Project Grant from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279) effective May 1, 2025 through April 30, 2027. The award supports development of an artificial intelligence (AI) platform designed to discover new therapeutics for substance use disorders (SUDs). The primary deliverables include: (1) curated training datasets and machine learning (ML) models to...
- The University of Texas Health Science Center at Houston received a $1.4 million Project Grant (R01 Stage IIA) from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279) awarded June 15, 2025, with a completion date of February 28, 2029. This pilot mechanistic study will investigate the repurposing of semaglutide, a glucagon-like peptide-1 receptor agonist (GLP-1RA), as a pharmacological treatment for cocaine use disorder (CUD). The research will...
- This cooperative agreement, awarded by the National Institute on Drug Abuse (NIDA) under the Drug Use and Addiction Research Programs (CFDA 93.279), provides $1.8M in funding to Lovelace Biomedical Research Institute to investigate neuromodulation as an adjunct to enhance the efficacy of motivational interviewing (MI) for substance use disorder (SUD) treatment. The project, which commenced September 30, 2025 and concludes August 31, 2027, will deliver research services examining transcranial...
- This Project Grant award from the National Institute on Drug Abuse (NIDA), under the Drug Use and Addiction Research Programs (CFDA 93.279), is supporting the development of a software-based medical device (SAMD) for detecting opioid use through voice analysis. The $800,000 award to Tenvos Inc., a minority-owned and woman-owned technology company, aims to advance the company's AI-driven solution that can enable patients to remotely test for opioid use and securely share results with...
- This $319,547 project grant awarded on September 15, 2023 by the National Institute on Drug Abuse (NIDA) under the Drug Abuse and Addiction Research Programs (CFDA 93.279) supports Afasci, Inc.'s research and development of a novel treatment for cocaine use disorder (CUD). The project will investigate the effects of Afasci's investigational new drug AFA-281, which inhibits both the T-type Cav3 ion channels and soluble epoxide hydrolase, on reducing cocaine-seeking behavior and hyperlocomotion in...
- Iontx Inc. received a $400,000 Project Grant award from the National Institute on Drug Abuse (NIDA) under the Drug Use and Addiction Research Programs (CFDA 93.279) to develop novel pharmacological treatments for cocaine use disorder (CUD). The award, issued on May 15, 2025, with a completion date of April 30, 2026, supports the optimization and preclinical evaluation of a first-in-class small-molecule modulator targeting the FGF13 (fibroblast growth factor 13) and NAV1.6 (voltage-gated sodium...
- This $512,256 Project Grant from the National Institutes of Health's National Institute on Drug Abuse will support Health Outcomes Inc. doing business as Telesage to develop a Primary Care-SUD Intake System (P-SUD-IS). The P-SUD-IS aims to address underdiagnosis of substance use disorders (SUDs) by streamlining the SUD assessment process for primary care clinicians. Telesage will create a HIPAA-compliant, automated, cloud-based system to facilitate completion of biopsychosocial assessments for...
- Federal Cooperative Agreement Summary Yale University received a $1.64M Cooperative Agreement from the National Institute on Drug Abuse under the Drug Use and Addiction Research Programs (CFDA 93.279) awarded July 15, 2025, for the development and validation of the Stimulant Use Disorder Severity Scale (STUDSS). This project addresses a critical gap in medication development for stimulant use disorder (STUD) by creating a novel clinical outcome assessment tool qualified by the U.S. Food and Drug...
- Federal Cooperative Agreement Summary The National Institute on Drug Abuse (NIDA) awarded a $6.24 million Cooperative Agreement to the University of Texas Health Science Center at Houston on September 15, 2025, under the Drug Use and Addiction Research Programs (CFDA 93.279) to conduct a clinical research study evaluating a novel treatment combination for cocaine use disorder (CUD). The research will combine contingency management (CM), a behavioral therapy approach, with deep transcranial...
DEVELOPMENT OF THE AI-DRIVEN MODEL FOR ANTI-SUD DRUG DEVELOPMENT BASED ON NEURONAL PLASTICITY - PROJECT SUMMARY RATES OF STIMULANT USE, BOTH ILLICIT (E.G. METHAMPHETAMINE AND COCAINE) AND PRESCRIPTION (E.G. ADDERALL) ARE SURGING ON THE HEELS OF THE OPIOID EPIDEMIC, WORSENED BY THE ISOLATION ASSOCIATED WITH THE COVID-19 PANDEMIC. UNLIKE OPIOID USE DISORDER, THERE ARE CURRENTLY NO FDA-APPROVED MEDICATIONS FOR THE TREATMENT OF STIMULANT USE DISORDER (STUD), LEAVING ONLY ABSTINENCE SUPPORT AND BEHAVIORAL MODIFICATION THERAPIES. THESE ARE COSTLY TREATMENTS WITH POOR EFFICACY, AS EVIDENCED BY THE HIGH RATE OF RELAPSE (60-90%). STIMULANT USE DISORDER IS CLEARLY AN UNMET NEED. VERISIM LIFE IS AN INNOVATIVE COMPANY DEVELOPING AND UTILIZING ARTIFICIAL INTELLIGENCE (AI) AND MACHINE LEARNING (ML) TECHNOLOGIES FOR FASTER DRUG DISCOVERY AND DEVELOPMENT. OUR PATENTED BIOISIM PLATFORM ENABLES PREDICTION OF SMALL MOLECULE PHARMACOKINETICS AND PHARMACODYNAMICS VIA AN AI/ML-PARAMETERIZED WHOLE-BODY PHYSIOLOGICALLY BASED MODELLING. IT IS DESIGNED TO ACCURATELY PREDICT THE CLINICAL VALUE OF INVESTIGATIONAL DRUGS BEFORE HUMAN TRIALS. THE FULL-STACK AI- ENABLED BIO-SIMULATION MODELS SIGNIFICANTLY REDUCE THE NUMBER OF ANIMAL TESTS REQUIRED FOR ADVANCING THERAPEUTICS THROUGH THE PIPELINE, ACCELERATING DRUG DEVELOPMENT AND MARKEDLY INCREASING RETURN ON INVESTMENT. THE PRIMARY GOAL OF THIS SBIR APPLICATION IS TO DEVELOP, VALIDATE AND UTILIZE A RELIABLE AND ACCURATE AI-DRIVEN TOOL INCORPORATED WITH THE CORE BIOISIM PLATFORM TO ACCELERATE DISCOVERY AND DEVELOPMENT OF PHARMACEUTICALS INTENDED FOR THE MITIGATION OF STUD. THE CURRENT PHASE I PROPOSAL WILL BEGIN TO ADDRESS THIS GOAL THROUGH TWO COMPLEMENTARY APPROACHES. DEVELOPMENT OF THE AI-DRIVEN PHARMACOKINETIC MODELING SPECIFIC TO CNS DRUG DISTRIBUTION WITH THE FOLLOWING SCREENING OF VIRTUAL COMPOUND LIBRARIES WILL BE PERFORMED IN AIM 1. THIS WILL BE SUPPORTED BY PROOF-OF-CONCEPT VALIDATION OF A SUBSET OF COMPOUNDS WITH IN VIVO PHARMACOKINETICS. AIM 2 WILL FOCUS ON DEVELOPMENT OF PHARMACODYNAMICS PREDICTION MODELING FOR STIMULANT USE DISORDER DRUG DISCOVERY AND DEVELOPMENT. THE FOCUS WILL BE ON POTENTIAL THERAPEUTIC TARGETS THAT MODULATE NEURONAL PLASTICITY, IDENTIFIED THROUGH AN IN-DEPTH ANALYSIS OF THE PRECLINICAL AND CLINICAL LITERATURE. THIS WILL BE SUPPORTED BY PROOF-OF-CONCEPT VALIDATION OF A SUBSET OF COMPOUNDS WITH PRECLINICAL INTRAVENOUS SELF-ADMINISTRATION STUDIES USING COCAINE AND METHAMPHETAMINE. THE PROPOSED AI/ML-DRIVEN APPROACH IS EXPECTED TO MARKEDLY ACCELERATE THE DEVELOPMENT PROCESS FOR NEW STIMULANT USE DISORDER MEDICATIONS BY DIRECTING EFFORTS TO COMPOUNDS WITH OPTIMAL ADME AND PHARMACODYNAMIC PROPERTIES. SUCH AN APPROACH WILL CREATE AN AVENUE FOR FAST-TRACK DEVELOPMENT OF AFFORDABLE AND EFFICACIOUS THERAPEUTICS FOR STUD AMONG OTHER INDICATIONS.
Mod # | Description | ReasonForModification | Federal Obligation | Date |
|---|---|---|---|---|
| Not listed | $0 | 3/4/24 | ||
| Not listed | $0 | 3/29/23 | ||
| Not listed | $0 | 3/29/23 | ||
| Not listed | $312.3k | 3/17/22 | ||
| Not listed | $312.3k | 3/17/22 |