COMPLETED

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

Study Overview

This clinical trial focuses on testing the efficacy of different digital interventions to promote re-engagement in cancer-related long-term follow-up care for adolescent and young adult (AYA) survivors of childhood cancer.

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.

Official Title

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

Quick Facts

Study Start:2022-01-27
Study Completion:2026-01-07
Study Type:Not specified
Phase:Not Applicable
Enrollment:Not specified
Status:COMPLETED

Study ID

NCT05251259

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.

Ages Eligible for Study:18 Years to 80 Years
Sexes Eligible for Study:ALL
Accepts Healthy Volunteers:No
Standard Ages:ADULT, OLDER_ADULT
Inclusion CriteriaExclusion Criteria
  1. Age 18 years or older
  2. Willing and able to provide informed consent
  3. Able to understand and follow study procedures
  4. Stable medical condition
  1. Pregnancy or breastfeeding
  2. Severe psychiatric disorders
  3. Active substance abuse
  4. Unstable medical conditions
  5. Inability to comply with study requirements

Contacts and Locations

Study Locations (Sites)

Research Site
Birmingham, Alabama, 35211
United States
Research Site
Sheffield, Alabama, 35660
United States
Research Site
Phoenix, Arizona, 85020
United States
Research Site
Tucson, Arizona, 85741
United States
Research Site
Little Rock, Arkansas, 72212
United States
Research Site
Bakersfield, California, 93301
United States
Research Site
Fountain Valley, California, 92708
United States
Research Site
Huntington Beach, California, 92647
United States
Research Site
Los Angeles, California, 90025
United States
Research Site
Newport Beach, California, 92663
United States
Research Site
San Jose, California, 95117
United States
Research Site
Valencia, California, 91355
United States
Research Site
Colorado Springs, Colorado, 80907
United States
Research Site
Cutler Bay, Florida, 33157
United States
Research Site
Cutler Bay, Florida, 33189
United States
Research Site
Hialeah, Florida, 33012
United States
Research Site
Hialeah, Florida, 33015
United States
Research Site
Hialeah, Florida, 33016
United States
Research Site
Miami, Florida, 33125
United States
Research Site
Miami, Florida, 33155
United States
Research Site
Miami, Florida, 33173
United States
Research Site
Miami, Florida, 33174
United States
Research Site
Orlando, Florida, 32807
United States
Research Site
Tampa, Florida, 33613
United States
Research Site
Tampa, Florida, 33615
United States
Research Site
Fayetteville, Georgia, 30214
United States
Research Site
Lithonia, Georgia, 30038
United States
Research Site
Savannah, Georgia, 31406
United States
Research Site
Boise, Idaho, 83706
United States
Research Site
Lexington, Kentucky, 40509
United States
Research Site
Owensboro, Kentucky, 42301
United States
Research Site
Oxon Hill, Maryland, 20745
United States
Research Site
New Bedford, Massachusetts, 02740
United States
Research Site
Ann Arbor, Michigan, 48105
United States
Research Site
Farmington Hills, Michigan, 48336
United States
Research Site
Saint Charles, Missouri, 63301
United States
Research Site
St Louis, Missouri, 63141
United States
Research Site
East Orange, New Jersey, 07018
United States
Research Site
Toms River, New Jersey, 08755
United States
Research Site
The Bronx, New York, 10459
United States
Research Site
Valhalla, New York, 10595
United States
Research Site
Charlotte, North Carolina, 28210
United States
Research Site
Charlotte, North Carolina, 28287
United States
Research Site
Gastonia, North Carolina, 28054
United States
Research Site
Wilmington, North Carolina, 28401
United States
Research Site
Blue Ash, Ohio, 45242
United States
Research Site
Dayton, Ohio, 45439
United States
Research Site
Edmond, Oklahoma, 73034
United States
Research Site
Pittsburgh, Pennsylvania, 15241
United States
Research Site
Columbia, South Carolina, 29204
United States
Research Site
Greenville, South Carolina, 29615
United States
Research Site
Spartanburg, South Carolina, 29303
United States
Research Site
Austin, Texas, 78705
United States
Research Site
Beaumont, Texas, 77701
United States
Research Site
Bellaire, Texas, 77401
United States
Research Site
Dallas, Texas, 75225
United States
Research Site
El Paso, Texas, 79902
United States
Research Site
El Paso, Texas, 79903
United States
Research Site
Houston, Texas, 77022
United States
Research Site
McKinney, Texas, 75069
United States
Research Site
San Antonio, Texas, 78258
United States
Research Site
Sugar Land, Texas, 77479
United States
Research Site
Tomball, Texas, 77375
United States
Research Site
Milwaukee, Wisconsin, 53228
United States

Collaborators and Investigators

Sponsor: AstraZeneca

Study Record Dates

These dates track the progress of study record and summary results submissions to ClinicalTrials.gov. Study records and reported results are reviewed by the National Library of Medicine (NLM) to make sure they meet specific quality control standards before being posted on the public website.

Study Registration Dates

Study Start Date2022-01-27
Study Completion Date2026-01-07

Study Record Updates

Study Start Date2022-01-27
Study Completion Date2026-01-07

Terms related to this study

Keywords Provided by Researchers

  • Efficacy
  • Safety
  • Multiple Dose Levels
  • Adults

Additional Relevant MeSH Terms

  • Asthma