Assess the efficacy, safety and tolerability of dexpramipexole in severe eosinophilic asthma EXHALE2

  • Research type

    Research Study

  • Full title

    A randomized, double-blind, placebo-controlled, parallel group study to assess the efficacy, safety, and tolerability of dexpramipexole administered orally for 52 weeks in participants with severe eosinophilic asthma (EXHALE-2)

  • IRAS ID

    1006607

  • Contact name

    Andrew Friedman

  • Contact email

    andrew.friedman@populationhp.com

  • Sponsor organisation

    Areteia Therapeutics, Inc.

  • Eudract number

    2022-003004-33

  • Clinicaltrials.gov Identifier

    NCT05763121

  • Research summary

    About half of people with asthma have “eosinophilic asthma”, which is a type of asthma with high levels of eosinophils, a type of white blood cell. These eosinophils can be measured in the blood and identify patients in which these cells play a role in their asthma and whose asthma
    improves with the eosinophil-lowering treatments below. In patients with eosinophilic asthma, eosinophils in the lung can release chemicals that lead to asthma symptoms and severe asthma attacks.
    Over the past several years, a few new drugs that lower eosinophils were approved by the U.S., UK and European medicines regulators (FDA, MHRA, EMA) for the treatment of asthma (for example, mepolizumab/Nucala; reslizumab/Cinqair; benralizumab/Fasenra). All of these
    approved drugs are injected using a needle.
    Dexpramipexole is an experimental drug that is an oral tablet that is taken by mouth twice a day but is not approved in any country. Dexpramipexole also works by lowering the number of eosinophils in the blood. In a Phase 2 study, Dexpramipexole lowered blood eosinophils and patients also experienced some improvement in their lung function. The Phase III programme for Dexpramipexole includes three studies - EXHALE-2, EXHALE-3 and EXHALE-4.
    EXHALE-2 is a 52-week study testing whether adding a new drug called Dexpramipexole, on top of standard inhaled medications, reduces the number of asthma attacks in people with severe eosinophilic asthma. Dexpramipexole will be compared to an inactive pill called a placebo. The purpose of this study is to understand more about the safety of Dexpramipexole and how well it works for the treatment of severe eosinophilic asthma.

  • REC name

    London - London Bridge Research Ethics Committee

  • REC reference

    22/LO/0780

  • Date of REC Opinion

    6 Feb 2023

  • REC opinion

    Further Information Favourable Opinion