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Safety and tolerability of srx246, a vasopressin 1a antagonist, in irritable huntingtonâs disease patientsâa randomized phase 2 clinical trial
SRX246 is a vasopressin (AVP) 1a receptor antagonist that crosses the bloodâbrain barrier. It reduced impulsive aggression, fear, depression and anxiety in animal models, blocked the actions of intranasal AVP on aggression/fear circuits in an experimental medicine fMRI study and demonstrated excellent safety in Phase 1 multipleâascending dose clinical trials. The present study was a 3âarm, multicenter, randomized, placeboâcontrolled, doubleâblind, 12âweek, dose escalation study of SRX246 in early symptomatic Huntingtonâs disease (HD) patients with irritability. Our goal was to determine whether SRX246 was safe and well tolerated in these HD patients given its potential use for the treatment of problematic neuropsychiatric symptoms. Participants were randomized to receive placebo or to escalate to 120 mg twice daily or 160 mg twice daily doses of SRX246. Assessments included standard safety tests, the Unified Huntingtonâs Disease Rating Scale (UHDRS), and exploratory measures of problem behaviors. The groups had comparable demographics, features of HD and baseline irritability. Eightyâtwo out of 106 subjects randomized completed the trial on their assigned dose of drug. Oneâsided exactâmethod confidence interval tests were used to reject the null hypothesis of inferior tolerability or safety for each dose group vs. placebo. Apathy and suicidality were not affected by SRX246. Most adverse events in the active arms were considered unlikely to be related to SRX246. The compound was safe and well tolerated in HD patients and can be moved forward as a candidate to treat irritability and aggression. © 2020 by the authors. Licensee MDPI, Basel, Switzerland.Open access journalThis item from the UA Faculty Publications collection is made available by the University of Arizona with support from the University of Arizona Libraries. If you have questions, please contact us at [email protected]