Verona Pharma's pMDI Ensifentrine Shows Improved Lung Function In Mid-Stage COPD Study

  • Verona Pharma PLC VRNA has reported positive data from the Phase 2 study evaluating pressurized metered-dose inhaler formulation (pMDI) of ensifentrine in moderate to severe chronic obstructive pulmonary disease. The study met all primary and secondary endpoints. 
  • Dose-ordered improvement in lung function was observed and statistically significant at peak and over the 12-hour dosing interval compared with placebo, thus supporting twice-daily dosing.
  • An increase in lung function measured by peak forced expiratory volume in one second (FEV1) were 205 mL, 277mL, and 326mL for 300 µg, 1000 µg, and 3000 µg dose, respectively.
  • Ensifentrine pMDI formulation was well tolerated at each dose with an adverse event profile similar to placebo.
  • The drug candidate is also under development in hospitalized COVID-19 patients, with results expected in Q2 this year.
  • Price Action: VRNA shares are higher by 13.4% at $8.96 in the pre-market session on the last check Tuesday.

Posted In: chronic obstructive pulmonaryPhase 2 Clinical TrialBiotechNewsSmall CapFDATop StoriesGeneral

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