Biopharma Transcript

ARS Pharmaceuticals, Inc. SPRY

Nasdaq · Phase 2 · immunology/inflammation · device-combination · EDGAR · Updated Oct 24, 2026

ARS Pharmaceuticals, Inc. (Nasdaq: SPRY) is an immunology/inflammation drug developer. Its lead program, neffy (intranasal epinephrine), is in Phase 2 for emergency treatment of Type I allergic reactions including anaphylaxis. Its next catalyst on record is neffy: Canadian commercial launch by partner ALK (2026).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: neffy — Canadian commercial launch by partner ALK (2026). 2 catalysts on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
neffy 2 mg / 1 mg (US)Type I allergic reactions including anaphylaxisdevice-combinationApproved
ARS-2 (intranasal epinephrine) Phase 2bacute flares in chronic spontaneous urticaria (CSU)device-combinationPhase 2

Recent results and decisions

  1. May 15, 2026
    approval FDA approved removing the age criteria from the 1 mg neffy label in late March 2026, so all patients weighing 33 lbs or more can use it.FDA approved removing the age criteria in late March 2026, so all children and adults who weigh 33 lbs or more can utilize neffy for the emergency treatment of Type I allergic reactions, including anaphylaxis. Filing
  2. Apr 15, 2026
    approval Health Canada approved neffy on April 15, 2026 (ex-US regulator); commercial launch by ALK expected later in 2026.On April 15, 2026, Health Canada approved neffy as the first and only needle-free emergency treatment for allergic reactions, including anaphylaxis, in Canada. Filing
  3. Mar 31, 2026
    approval European Commission granted marketing authorization for EURneffy 1 mg on March 31, 2026 (ex-US regulator).On March 31, 2026, the European Commission granted marketing authorization for EURneffy® 1 mg, extending the neffy franchise across the EU Filing

2 more on record.

For subscribers

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