7. PROJECT SUMMARY Our SBIR Phase I proposal focuses on preclinical proof of concept studies on our IND AFA-281 for treatment cocaine use disorder (CUD). AFA-281 is a new chemical entity discovered by AfaSci that inhibits both the T-type Cav3 channels and soluble epoxide hydrolase (sEH). T-type channels consist of Cav3.1, 3.2, and 3.3 subunits. Cocaine activates ion channels, including T-channels in the brain to increase neuronal excitability and alter synaptic neurotransmission. Mibefradil, an old T-channel inhibitor blocks cocaine-induced GABAergic abnormalities and hyperlocomotion in mice. Studies in Cav3.1 knockout mice revealed T-type channels play a major role in sustaining ventral tegmental area neuronal excitability, and Cav3.2-deficient mice display reduced psychostimulant sensitivity. Hence, two Cav3 subunits are biologically validated as CUD drug targets. Recent studies suggest an involvement of neuroinflammation in addiction. Single sEH inhibitors or sEH genetic deletion show a reduction in neuroinflammation. Although sEH involvement in CUD is unknown, we hypothesize our dual inhibitor of Cav3/sEH could suppress cocaine-induced hyperexcitability and neuroinflammation, and thereby be an effective treatment for CUD. The goal of this project is to test this feasibility. This project’s innovation lies in AfaSci’s discovery of a series of patented dual modulators of Cav3 channels and sEH with a favorable druggable profile. AfaSci completed lead identification through rational drug design, iterative screenings using patch-clamp recordings and enzymatic assays. Lead optimization was conducted through 81 off-drug target selectivity screening and demonstrated no cardiac safety concerns using human cardiomyocytes in vitro. Based on pharmacokinetic and pharmacodynamic (PK/PD) studies, AFA-281 has shown an excellent oral bioavailability (70% in rats and 92% in dogs), acceptable t1/2 (2.5-4.3 h), CNS penetration, broad analgesic effects and good safety margins. Upon completion of the IND-enabling studies, AFA-281’s IND application was recently accepted by the FDA for a primary indication in neuropathic pain. In Preliminary Studies, we have shown cocaine-enhanced neural excitability was blocked by AFA-281 in rat thalamocortical slices. Rat cocaine-seeking behavior indicated by self-administration (SA) of intravenous (IV) infusion of cocaine solution was suppressed by AFA-281, and cocaine-elicited hyperlocomotion in rats and mice were restored to control levels by AFA-281. Our Specific Aim 1 in this project is to rigorously investigate AFA-281’s effects on rat intentional drug seeking via SA of IV infusion of cocaine in acquisition training and compulsive reward seeking under progress ratio schedule and on reinstatement in relapse. Our Specific Aim 2 is to investigate PK/PD of AFA-281 for suppressing cocaine seeking behavior and cocaine-induced hyperlocomotion in rats. Success in SBIR Phase I project will demonstrate proof of concept, leading to clinical development of AFA-281 for a secondary indication in CUD with an SBIR Phase II project and/or with third party support. Ultimately, AFA-281 as a safe, effective, and accessible medication will mitigate CUD.

8. PROJECT NARRATIVE AfaSci is developing a drug candidate that has been granted investigational new drug (IND) status by the FDA. This drug can normalize neural activity and enhance anti-inflammatory ability. We now propose to test its efficacy in animal models of cocaine use disorder to provide an evidence base for future clinical development of this IND into a safe and effective medication for cocaine use disorder.