Study to Assess the Efficacy and Safety of Atuliflapon in Moderate-to-Severe Uncontrolled Asthma

Description

This is a randomised, placebo-controlled, double-blind study to assess the efficacy and safety of Atuliflapon administered once daily over a 12-week treatment period to adult participants with moderate to severe uncontrolled asthma.

Conditions

Asthma

Study Overview

Study Details

Study overview

This is a randomised, placebo-controlled, double-blind study to assess the efficacy and safety of Atuliflapon administered once daily over a 12-week treatment period to adult participants with moderate to severe uncontrolled asthma.

A Phase 2a, Randomised, Double-Blind, Placebo-Controlled Study to Assess Efficacy and Safety of Atuliflapon Given Orally Once Daily for Twelve Weeks in Adults With Moderate to Severe Uncontrolled Asthma

Study to Assess the Efficacy and Safety of Atuliflapon in Moderate-to-Severe Uncontrolled Asthma

Condition
Asthma
Intervention / Treatment

-

Contacts and Locations

Birmingham

Research Site, Birmingham, Alabama, United States, 35211

Sheffield

Research Site, Sheffield, Alabama, United States, 35660

Phoenix

Research Site, Phoenix, Arizona, United States, 85020

Tucson

Research Site, Tucson, Arizona, United States, 85741

Little Rock

Research Site, Little Rock, Arkansas, United States, 72212

Bakersfield

Research Site, Bakersfield, California, United States, 93301

Fountain Valley

Research Site, Fountain Valley, California, United States, 92708

Fullerton

Research Site, Fullerton, California, United States, 92835

Huntington Beach

Research Site, Huntington Beach, California, United States, 92647

Los Angeles

Research Site, Los Angeles, California, United States, 90025

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

    Ages Eligible for Study

    18 Years to 80 Years

    Sexes Eligible for Study

    ALL

    Accepts Healthy Volunteers

    No

    Collaborators and Investigators

    AstraZeneca,

    Study Record Dates

    2026-01-29