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 Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of AVTX-002 for the Treatment of Poorly Controlled Non-Eosinophilic Asthma

Trial Profile

A Phase 2, Randomized, Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate the Safety and Efficacy of AVTX-002 for the Treatment of Poorly Controlled Non-Eosinophilic Asthma

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 09 Sep 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 Quisovalimab (Primary)
  • Indications Asthma
  • Focus Proof of concept; Therapeutic Use
  • Acronyms PEAK
  • Sponsors Avalo Therapeutics
  • Most Recent Events

    • 20 Jul 2023 Status changed from active, no longer recruiting to completed.
    • 26 Jun 2023 Primary endpoint (To assess the ability of AVTX-002 to improve asthma control in subjects with poorly controlled non- eosinophilic asthma (NEA) based on the proportion of patients who experience asthma related events.) has not been met as per Avalo Therapeutics Media Release
    • 26 Jun 2023 Results published in the Avalo Therapeutics Media Release

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

If your organization or you do not have a subscription, try one of the following:
  • Contacting your organization’s admin about adding this content to your AdisInsight subscription
  • Buying a PDF version of any individual profile
  • Request a free trial
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