AB-300 is under development by Ariadne Bio, a company of Negev Labs.[1][2][3] Ariadne Bio is named after Ariadne (4C-D; BL-3912; Dimoxamine), a non-hallucinogenic serotonin 5-HT2A receptor agonist which was developed by Alexander Shulgin and Bristol Laboratories, produced indirect dopaminergic and pro-motivational effects in animals analogously to AB-300, and reached phase 3clinical trials for various medical uses in the 1970s, but was ultimately never marketed due to cited strategic economic reasons.[7][8][9][10] A phase 1b trial of AB-300 is initiating in the third quarter of 2026.[2][3] The exact chemical structure of AB-300 does not yet appear to have been disclosed, but it is said to have been patented.[1][2]
^ abcd"Ariadne Bio". Ariadne Bio. Retrieved 9 August 2026. Ariadne Bio is the first company from Negev Labs, [...] AB-300 is designed to activate 5-HT2A without hallucinogenic effect, potentially making it an accessible and self-administered therapy for motivational deficits. [...] Patented. Randomized, placebo-controlled Phase 1b trial in Parkinson's disease patients with clinically significant apathy. [...] Phase 1b clinical trial initiating Q3 2026
^ abcNegev Labs. "CNS & Brain Health Therapeutics Venture Fund". Negev Capital. Retrieved 9 August 2026. Ariadne Bio is developing AB-300, a first-in-class non-hallucinogenic 5-HT2A agonist designed to treat apathy in Parkinson's disease, late-life depression, and neurodegeneration [...] Phase 1b trial initiation targeted for Q3 2026. [...] Stage Preclinical → Phase 1b Q3 2026 · Modality Non-hallucinogenic 5-HT2A agonist · Indication Apathy in Parkinson's / late-life depression
^Mori T, Shibasaki M, Ogawa Y, Hokazono M, Wang TC, Rahmadi M, et al. (October 2013). "Comparison of the behavioral effects of bupropion and psychostimulants". European Journal of Pharmacology. 718 (1–3): 370–375. doi:10.1016/j.ejphar.2013.07.046. PMID23993950.
^Naglich AC, Brown ES, Adinoff B (2019). "Systematic review of preclinical, clinical, and post-marketing evidence of bupropion misuse potential". The American Journal of Drug and Alcohol Abuse. 45 (4): 341–354. doi:10.1080/00952990.2018.1545023. PMID30601027.
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