Evaluation of Dupilumab in Patients With Persistent Asthma (Liberty Asthma Quest)

Completed · Phase 3 · Has a placebo group

Conditions studied: Asthma

In brief

Primary Objective: To evaluate the efficacy of dupilumab (SAR231893 / REGN668) in participants with persistent asthma. Secondary Objectives: * To evaluate the safety and tolerability of dupilumab. * To evaluate the effect of dupilumab on improving participant-reported outcomes including health-related quality of life. * To evaluate dupilumab systemic exposure and incidence of anti-drug antibodies.

Key facts

Study ID

NCT02414854

Run by

Sanofi

People needed

1902

Starts

2015-04-27

Expected to finish

2017-11-23

Last updated by the study team

2018-10-23

Who can join

Age: 12 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• Adults and adolescent participants with a physician diagnosis of asthma for ≥12 months, based on the Global Initiative for Asthma (GINA) 2014 Guidelines and the following criteria:
• a) Existing treatment with medium to high dose ICS (≥250 mcg of fluticasone propionate twice daily or equipotent ICS daily dosage to a maximum of 2000 mcg/day of fluticasone propionate or equivalent) in combination with a second controller (eg, long-acting beta agonist, leukotriene receptor antagonist) for at least 3 months with a stable dose ≥1 month prior to Visit 1.
• i) Note for Japan: for participants aged 18 years and older, ICS must be on ≥200 mcg of fluticasone propionate twice daily or equivalent; for participants aged 12 to 17 years, ICS must be ≥100 mcg of fluticasone propionate twice daily or equivalent).
• ii) Participants requiring a third controller for their asthma will be considered eligible for this study, and it should also be used for at least 3 months with a stable dose ≥1 month prior to Visit 1.

You may not qualify if…

• Participants <12 years of age or the minimum legal age for adolescents in the country of the investigative site, whichever is higher (For those countries where local regulations permit enrollment of adults only, participant recruitment will be restricted to those who are ≥18 years of age).
• Weight is less than 30 kilograms.
• Chronic obstructive pulmonary disease or other lung diseases (eg, idiopathic pulmonary fibrosis, Churg-Strauss Syndrome, etc) which may impair lung function.
• A participant who experiences a severe asthma exacerbation (defined as a deterioration of asthma that results in emergency treatment, hospitalization due to asthma, or treatment with systemic steroids at any time from 1 month prior to the Screening Visit up to and including the Baseline Visit).
• Evidence of lung disease(s) other than asthma, either clinical evidence or imaging (Chest X-ray, CT, MRI) within 12 months of Visit 1 or at the screening visit, as per local standard of care.
• Note for Japan: According to the request from the health authority, chest X-ray should be performed at screening visit if there is no chest imaging (Chest X-ray, computed tomography [CT], magnetic resonance imaging [MRI]) available within 3 months prior to screening to exclude participants with suspected active or untreated latent tuberculosis.
• Current smoker or cessation of smoking within 6 months prior to Visit 1.
• Previous smoker with a smoking history >10 pack-years.
• Comorbid disease that might interfere with the evaluation of Investigational Medicinal Product.
• The above information is not intended to contain all considerations relevant to a participant's potential participation in a clinical trial.

Where it is running

• Investigational Site Number 840056 — Flagstaff, Arizona, United States
• Investigational Site Number 840099 — Gilbert, Arizona, United States
• Investigational Site Number 840087 — Scottsdale, Arizona, United States
• Investigational Site Number 840132 — Little Rock, Arkansas, United States
• Investigational Site Number 840109 — Bakersfield, California, United States
• Investigational Site Number 840052 — Costa Mesa, California, United States
• Investigational Site Number 840116 — Fresno, California, United States
• Investigational Site Number 840045 — Long Beach, California, United States
• Investigational Site Number 840011 — Los Angeles, California, United States
• Investigational Site Number 840061 — Los Angeles, California, United States
• Investigational Site Number 840097 — Los Angeles, California, United States
• Investigational Site Number 840019 — Mission Viejo, California, United States
• Investigational Site Number 840125 — Newport Beach, California, United States
• Investigational Site Number 840041 — North Hollywood, California, United States
• Investigational Site Number 840036 — Redwood City, California, United States
• Investigational Site Number 840020 — Rolling Hills Estates, California, United States
• Investigational Site Number 840074 — Roseville, California, United States
• Investigational Site Number 840021 — San Jose, California, United States
• Investigational Site Number 840004 — Centennial, Colorado, United States
• Investigational Site Number 840025 — Colorado Springs, Colorado, United States
• Investigational Site Number 840034 — Denver, Colorado, United States
• Investigational Site Number 840130 — Denver, Colorado, United States
• Investigational Site Number 840102 — New Haven, Connecticut, United States
• Investigational Site Number 840037 — Aventura, Florida, United States
• Investigational Site Number 840047 — Birmingham, Alabama, United States

Full record on ClinicalTrials.gov

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