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Friday, February 25, 2022

Aquestive Highlights Early Data From Allergy Treatment Candidate

 Aquestive Therapeutics Inc 

 (Get Free Alerts for AQST) announced positive topline results from Part 1 of the EPIPHAST study for its AQST-109 epinephrine oral film. 

  • Part 1 showed that key pharmacokinetic measures were aligned with previous favorable results for AQST-109 and that the product was well tolerated with no serious adverse events. 
  • A lead candidate is currently being evaluated in Part 2 of the EPIPHAST study.
  • The lead formulation of AQST-109 rapidly reached clinically meaningful blood concentrations when delivered in two different physical configurations, with a median Tmax of 13.5 minutes and 22.5 minutes, respectively. 
  • Part 1 data also demonstrated that arithmetic mean maximum concentrations values consistent with those previously reported for approved injectable epinephrine devices such as EpiPen.
  • EPIPHAST is a crossover study in healthy adult subjects comparing the pharmacokinetics and pharmacodynamics of epinephrine delivered via Aquestive's AQST-109 oral film compared to intramuscular injection of epinephrine.
  • Aquestive has commenced Part 2 of the EPIPHAST study and expects to report topline results in the first half of 2022. 
  • Part 2 is a randomized, crossover design comparing AQST-109 12mg to epinephrine IM 0.3mg.

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