ARS Pharmaceuticals

ARS Pharmaceuticals

SPRY
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SPRY · Stock Price

USD 9.00-4.44 (-33.04%)
Market Cap: $896.2M

Historical price data

Market Cap: $896.2MPipeline: 5 drugsPatents: 4Founded: 2015HQ: San Diego, United States

Overview

ARS Pharmaceuticals is on a mission to transform the treatment of severe allergic reactions by developing needle-free, patient-friendly therapies. Its transformative achievement is the 2024 FDA approval of neffy®, the first needle-free epinephrine nasal spray, which directly tackles the underutilization of epinephrine due to fear, complexity, and portability issues with auto-injectors. The company's strategy is to commercialize neffy® in the substantial anaphylaxis market while advancing its intranasal platform into adjacent Type I hypersensitivity indications like urticaria, aiming to capture significant market share from entrenched auto-injector competitors.

Allergy & ImmunologyDermatology

Technology Platform

Proprietary intranasal delivery platform engineered to deliver therapeutic doses of epinephrine through the nasal mucosa, utilizing absorption enhancers to achieve rapid systemic pharmacokinetics comparable to intramuscular injection.

Pipeline

5
5 drugs in pipeline
DrugIndicationStageWatch
Neffy + AdrenalineAllergic ReactionsApproved
ARS-1 + PlaceboUrticariaPhase 2
ARS-1 + Albuterol MDI + PlaceboAsthmaPhase 2
Placebo + 0.5 mg epinephrine + 1 mg epinephrineUrticaria ChronicPhase 2
ARS-1 with URTI + ARS-1 without URTIUpper Respiratory Tract InfectionPhase 1

Funding History

3
Total raised:$195M
IPO$125M
Series B$45M
Series A$25M

FDA Approved Drugs

1
NEFFYNDAAug 9, 2024

Opportunities

The primary opportunity is capturing significant market share in the multi-billion dollar epinephrine market by addressing the critical 'carry and use' gap through a needle-free, patient-preferred product.
A secondary greenfield opportunity exists in developing the first FDA-approved rescue therapy for acute flares of chronic urticaria, a large and underserved patient population.

Risk Factors

Key risks include commercial execution failure in launching neffy®, intense competitive and pricing pressure from entrenched auto-injector incumbents, slower-than-expected market adoption by providers and payers, and the inherent clinical and regulatory risks associated with the early-stage urticaria pipeline program.

Competitive Landscape

ARS Pharma's direct competition consists of established epinephrine auto-injector brands (EpiPen, Auvi-Q, generics). Its competitive advantage is its first-mover status in the needle-free category, competing on usability and patient preference rather than price alone. In its pipeline urticaria indication, it faces less direct competition, targeting an unmet need for acute rescue therapy alongside chronic control agents.

Company Timeline

2015Founded

Founded in San Diego, United States

2017Series A

Series A: $25.0M

2020Series B

Series B: $45.0M

2022IPO

IPO — $125.0M

2024FDA Approval

FDA Approval: NEFFY