Efficacy And SafetyThe tolerability and safety profile of KPI-012 could be a differentiating factor, as patients reported significant pain relief during trials.
Market OpportunityWith no FDA approved treatment for PCED, KPI-012 could unlock real commercial potential.
Trial DesignThe unique 1-week run-in design of KALA's trial could lower the placebo effect, which is often a challenge in this space.