(Stockholm, 28 September 2021.) The publication of Asarina Pharma’s phase IIb study, including a post hoc analysis into Sepranolone for PMDD (Premenstrual dysphoric disorder), demonstrates that Sepranolone in a 10 mg dose did have a significant treatment effect compared with placebo, when examined in an extended 9-day analysis of symptom reduction. Senior PMDD Key Opinion Leaders who co-authored the publication include Dr Nick Panay (Imperial College London), Prof. Shaughn O’Brien (Royal Stoke University Hospital, UK), Prof. C. Neill Epperson (Dept. Psychiatry, University of Colorado), Prof Marie Bixo (Umeå University, Sweden) and Dr Angelica Lindén Hirschberg, Karolinska University Hospital, Stockholm, Sweden - together with Asarina Pharma CSO Prof Torbjörn Bäckström (Umeå University, Sweden).
Topline results for Asarina Pharma’s phase IIb study in Sepranolone for PMDD, released in April 2020, found that Sepranolone failed to meet its primary or secondary clinical endpoints in its 5-day targeted treatment period of the five worst premenstrual days, due to an unexpectedly high placebo effect. A post hoc analysis was undertaken to investigate the treatment effect during an extended 9 premenstrual days in the third treatment cycle (it has previously been shown that 9 premenstrual days may be more representative for comparison of PMDD symptom periods than the 5 worst premenstrual days). Data from this analysis were presented on February 12, 2021, and have now been published in the Journal of Psychoneuroendocrinology, titled A randomized, double-blind study on efficacy and safety of sepranolone in premenstrual dysphoric disorder (Bäckström et al.).
Asarina Pharma CEO Peter Nordkild: “As I commented when we first communicated the results in our 2020 Annual Report, these findings would be valuable to any larger pharma partner wishing to pursue future PMDD studies. We have been very clear that we do not intend to continue clinical development of Sepranolone for PMDD by ourselves - as a study needed to further corroborate these findings would realistically involve at least six months of therapy and likely several hundred patients - which is clearly beyond our current capabilities. Nevertheless, these data are exciting, and represent one of the most important and promising bodies of evidence to date when it comes to a pharmaceutical treatment for PMDD. They further clearly point towards allopregnanolone’s role as a key factor in triggering highly disruptive, mood-altering symptoms, including our current focus areas of Tourette and OCD - and confirm our confidence in Sepranolone as an important and effective modulator of allopregnanolone.”