Either you have JavaScript disabled or your browser does not support Javascript . To work properly, this page requires JavaScript to be enabled.
How to enable JavaScript in your browser?

A Single-Dose, Randomized, Placebo-Controlled, Cross-Over Study of the Safety and Efficacy of Intranasal Epinephrine After Administration of ARS -1 in Subjects With Frequent Urticaria Flares

Trial Profile

A Single-Dose, Randomized, Placebo-Controlled, Cross-Over Study of the Safety and Efficacy of Intranasal Epinephrine After Administration of ARS -1 in Subjects With Frequent Urticaria Flares

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 01 Aug 2024

Price :
$35 *
Note:
  • Adis is an information provider.
  • Final gross price and currency may vary according to local VAT and billing address.
  • Your purchase entitles you to full access to the information contained in our trial profile at the time of purchase.
  • A link to download a PDF version of the trial profile will be included in your email receipt.

At a glance

  • Drugs Epinephrine (Primary)
  • Indications Urticaria
  • Focus Proof of concept; Therapeutic Use
  • Sponsors ARS Pharmaceuticals

Most Recent Events

  • 30 Jul 2024 Status changed from active, no longer recruiting to completed.
  • 26 Feb 2024 Results assessing efficacy of ARS-2 in Urticaria Scores in Patients with Frequent Urticaria Flares presented at the 2024 Annual Meeting of the American Academy of Allergy, Asthma and Immunology
  • 26 Feb 2024 According to an ARS Pharmaceuticals media release, data for neffy are being presented on February 26, at the 2024 American Academy of Allergy, Asthma and Immunology (AAAAI) in Washington.

You need to be a logged in or subscribed to view this content

Request demo (opens in a new window)
If your organization or you do not have a subscription, try one of the following: If your organization has a subscription, there are several access options, even while working remotely:
  • Working within your organization’s network
  • with username/password or try to via your institution
  • Persisted access using your organization’s identifier stored in your user browser for 90 days
Back to top