Leerink Global Healthcare Conference 2026
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ARS Pharmaceuticals (SPRY) Leerink Global Healthcare Conference 2026 summary

Event summary combining transcript, slides, and related documents.

Logotype for ARS Pharmaceuticals Inc

Leerink Global Healthcare Conference 2026 summary

11 Mar, 2026

Strategic goals and market access

  • Aims for 90% commercial coverage for neffy by summer, focusing on securing large payers and expanding Medicaid access, with Florida expected to join soon.

  • Medicaid states are willing to pay over twice the price of EpiPen, representing 24-25% of the market.

  • Two main 2024 goals: expand neffy access for greater uptake and advance urticaria clinical development.

  • Commercial coverage is at 57% unrestricted, with 93% overall coverage; efforts ongoing to reduce prior authorization barriers.

  • Medicaid expansion expected to accelerate through 2024 as more states' P&T committees approve coverage.

Product uptake, patient dynamics, and prescriber experience

  • About 75% of neffy users are switching from auto-injectors, with 25% from new or previously unfilled prescriptions.

  • Pediatric use remains strong, with 55% of patients being children; pending removal of age restriction expected to boost younger patient uptake.

  • The neffy Experience program has driven high prescriber confidence and market share, with real-world data showing efficacy comparable to injection.

  • Virtual prescription and Getneffy.com initiatives reduce physician and patient burden, streamlining access and supporting refill dynamics.

  • DTC campaigns have raised consumer awareness from 20% to over 60%, with messaging now focused on practical benefits and ease of use.

Clinical development and pipeline progress

  • Phase 2b urticaria study is ongoing, with interim analysis expected in Q3 2024; Phase 3 targeted for mid-2027.

  • Early studies show rapid and significant itch relief in urticaria flares, supporting the rationale for intranasal epinephrine as an add-on therapy.

  • The urticaria indication is seen as a major value driver, with potential to reduce ER visits and biologic use, offering pharmacoeconomic benefits.

  • The urticaria program is considered low risk due to strong clinical evidence and expert support.

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