Roluperidone Explained

Roluperidone (former developmental code names MIN-101, CYR-101, MT-210) is a 5-HT2A and σ2 receptor antagonist under development by Minerva Neurosciences for the treatment of schizophrenia.[1] [2] [3] [4] One of its metabolites also has some affinity for the H1 receptor. Pre-clinical findings provide evidence of the effect of roluperidone on Brain-Derived Neurotrophic Factor (“BDNF”), which has been associated with neurogenesis, neuroplasticity, neuroprotection, synapse regulation, learning and memory.[5]

As of May 2018, the drug was in phase III clinical trials.[6] In May 2020, the shares of Minerva Neurosciences plummeted 67% after the trial "failed to meet its primary endpoint of reduction in negative symptoms, and key secondary endpoints of improvement in personal and social performance measurements."[7] However, in August 2022 Minerva submitted a New Drug Application (NDA) to the Food and Drug Administration (FDA) for the approval of roluperidone for the treatment of schizophrenia.[8] The NDA submission in 2022 followed successful completion of a phase III clinical trial which was published in early 2022. Minerva believed that the findings of this second trial supported the claim that the drug was an effective agent for the treatment of negative symptoms in schizophrenia. However, in October 2022, FDA sent Minerva a refusal to file letter pertaining to the New Drug Application for roluperidone for treating negative symptoms in schizophrenia patients. [9]

Chemistry

Synthesis

The Boc protection of 4-aminomethylpiperidine [7144-05-0] (1) gives tert-Butyl 4-aminomethylpiperidine-1-carboxylate hydrochloride [359629-16-6] (2). The free-radical halogenation of ethyl o-toluate [87-24-1] (3) led to ethyl 2-(bromomethyl)benzoate [7115-91-5] (4). The reaction between the two intermediates led to 2-[(1-tert-Butoxycarbonylpiperidin-4-yl)methyl]isoindolin-1-one [359629-19-9] (5). Deprotection yielded 2-(Piperidin-4-ylmethyl)-3H-isoindol-1-one;hydrochloride (6). Alkylation of the secondary nitrogen with 2-chloro-4'-fluoroacetophenone [700-35-6] (7) completed the synthesis of Roluperidone (8).

See also

Notes and References

  1. Mestre TA, Zurowski M, Fox SH . 5-Hydroxytryptamine 2A receptor antagonists as potential treatment for psychiatric disorders . Expert Opinion on Investigational Drugs . 22 . 4 . 411–21 . April 2013 . 23409724 . 10.1517/13543784.2013.769957 . 36268341 .
  2. Ebdrup BH, Rasmussen H, Arnt J, Glenthøj B . Serotonin 2A receptor antagonists for treatment of schizophrenia . Expert Opinion on Investigational Drugs . 20 . 9 . 1211–23 . September 2011 . 21740279 . 10.1517/13543784.2011.601738 . 438422 .
  3. Köster LS, Carbon M, Correll CU . Emerging drugs for schizophrenia: an update . Expert Opinion on Emerging Drugs . 19 . 4 . 511–31 . December 2014 . 25234340 . 10.1517/14728214.2014.958148 . 42729570 .
  4. Drug Development in Schizophrenia: Summary and Table. Pharmaceutical Medicine. 28. 5. 2014. 265–271. 1178-2595. 10.1007/s40290-014-0070-6. 256364393 .
  5. Web site: Roluperidone (MIN-101) • Minerva Neurosciences .
  6. Web site: Roluperidone - Minerva Neurosciences . Adis Insight . Springer Nature Switzerland AG .
  7. Web site: Kilgore. Tomi. Minerva Neurosciences' stock plummets after schizophrenia treatment disappoints in phase 3 study. 2021-03-21. MarketWatch. en-US.
  8. Web site: Minerva Neurosciences Submits New Drug Application to FDA for Roluperidone for the Treatment of Negative Symptoms in Patients with Schizophrenia .
  9. Web site: Minerva Neurosciences Receives Refusal to File Letter from FDA for its New Drug Application for Roluperidone for the Treatment of Negative Symptoms in Schizophrenia .