Epinephrine is under clinical development by ARS Pharmaceuticals and currently in Pre-Registration for Anaphylaxis. According to GlobalData, Pre-Registration drugs for Anaphylaxis have a 100% phase transition success rate (PTSR) indication benchmark for progressing into Marketed. GlobalData’s report assesses how Epinephrine’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.

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GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.

Epinephrine overview

Epinephrine (ARS-1) is under development for the treatment of anaphylaxis caused by severe allergic reactions to medications, insect bites, asthma, urticaria, seasonal allergic rhinitis, food allergy and infectious rhinitis. It is formulated as spray and administered through intranasal route. The drug candidate acts by targeting ADRA, ADRB adrenergic receptors. It is developed based on Intravail technology.

ARS Pharmaceuticals overview

ARS Pharmaceuticals (ARS Pharma) is a biopharmaceutical company that develops the treatments for severe allergic reactions. The company’s main product in development is a needle-free, low-dose intranasal epinephrine nasal spray intended for use as a rescue medication for people with Type 1 severe allergic reactions, including anaphylaxis. Its products include neffy. ARS Pharma’s products are designed for patients and caregivers that need a safe, effective, and easy-to-administer alternative to injectable devices. It serves customers across the US. ARS Pharma is headquartered in San Diego, California, the US.

For a complete picture of Epinephrine’s drug-specific PTSR and LoA scores, buy the report here.

This content was updated on 20 May 2024

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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.

GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.