Summary of KalVista Pharmaceuticals Conference Call Company Overview - Company: KalVista Pharmaceuticals - Product: Ekterly, an oral therapy for the on-demand treatment of acute attacks of Hereditary Angioedema (HAE) - FDA Approval: Received in July 2025, with a launch shortly thereafter [4][5] Key Points Product Launch and Market Penetration - Patient Adoption: Over 1,000 patients currently on Ekterly, representing over 10% of the market, with expectations to reach 12-13% [5][6] - Treatment Guidelines: Ekterly encourages early treatment of attacks, aligning with guidelines that suggest treating all attacks, even mild ones [6][7] - Patient Satisfaction: High satisfaction reported among patients, attributed to the convenience of oral administration [7] Prescription and Refill Mechanics - Initial Prescription Process: Patients receive a free drug sample and then transition to commercial coverage, which may take 6-8 weeks initially [10][14] - Refill Rates: Patients with severe disease (15-20% of the population) are the highest users, refilling every 3-4 weeks [17][18] - Stockpiling: Patients are expected to stockpile Ekterly due to its convenience, although dramatic stockpiling is not anticipated [28][29] Market Dynamics and Competition - Market Transition: The market is expected to shift towards oral therapies, reducing the reliance on injectables [24][44] - Pharvaris Competition: Upcoming data from Pharvaris is viewed as a data event for investors but is not expected to impact KalVista's commercial trajectory significantly [38][39] - Market Leadership: Confidence expressed in maintaining market leadership post-Pharvaris entry due to patient satisfaction and the advantages of Ekterly [44] International Expansion - Global Launch Plans: First shipment to Germany in October 2025, with launches in the U.K. and Japan expected in early 2026 [46] - Pricing Strategy: International pricing is anticipated to be significantly lower than U.S. pricing, with estimates around 20% of U.S. prices [48][52] Pediatric Market Insights - Pediatric Need: Approximately 500 pediatric patients in the U.S. with HAE, highlighting an unmet need for non-injectable therapies [57][58] - Efficacy in Pediatrics: Initial data shows that pediatric patients experience similar efficacy and safety profiles as adults, with previously unrecognized higher attack rates [59][60] Additional Insights - Patient Services: Robust patient services are in place, contributing to high patient retention and satisfaction [33] - Safety Profile: No significant adverse events reported post-launch, maintaining a pristine safety profile [35] This summary encapsulates the key aspects of KalVista Pharmaceuticals' conference call, focusing on the company's product, market dynamics, and future outlook.
KalVista Pharmaceuticals (NasdaqGM:KALV) 2025 Conference Transcript