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Completed

NCT Number: NCT01561690

A Study of ARRY-502 in Patients With Persistent Asthma

This is a Phase 2 study, involving a 6-week treatment period, designed to evaluate the effectiveness of investigational study drug ARRY-502 in treating mild to moderate persistent asthma, and to further evaluate the safety of the drug. Approximately 180 patients from the US will be enrolled in this study.

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Key information

Age range

18 year–70 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Allergy & Asthma Specialists Medical Group, Huntington Beach, California, United States

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Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Key Inclusion Criteria:

  • Documented history of bronchial asthma diagnosed at least 6 months prior to study start and prior to the age of 40 years.
  • Body mass index (BMI) of 18 to 35 inclusive.
  • An ACQ score of ≥ 1.5 at specified time points prior to first dose of study drug.
  • A best prebronchodilator FEV1 of 60% to 85% of the predicted normal value and a change in best postbronchodilator FEV1 of ≥ 12% and ≥ 200 mL at specified time points prior to first dose of study drug.
  • Additional criteria exist.

Key Exclusion Criteria:

  • Evidence of aspirin-sensitive asthma.
  • Pre-existing lung disease other than asthma.
  • Clinically significant dermatologic, hematological, renal, endocrine, pulmonary (other than asthma), gastrointestinal, cardiovascular, hepatic, neurologic, ophthalmologic, musculoskeletal or immunologic disease (excepting allergic disease and asthma) that is uncontrolled despite treatment or is likely in the opinion of the Investigator to require a change in therapy during the study.
  • Patients with any current or past history of cancer within 5 years prior to study start except for treated basal cell or squamous cell carcinomas of the skin, ductal carcinoma in situ of the breast or cervical carcinomas in situ.
  • Any history of serious illness requiring hospitalization within 6 months prior to study start.
  • Known positive serology for the human immunodeficiency virus (HIV), hepatitis B and/or active hepatitis C.
  • A positive test for drugs or alcohol, unless the positive drug screen is associated with a prescribed medication and is approved by the Medical Monitor.
  • Smoking (tobacco or marijuana) within 6 months prior to study start and/or a smoking history of > 10 packs/year.
  • Blood donation of ≥ 1 pint (473 mL) within 8 weeks prior to the first dose of study drug.
  • Previous treatment with ARRY-502.
  • Additional criteria exist.

Treatment and study plan

ARRY-502, CRTh2 antagonist; oral

Drug

multiple dose, single schedule

Placebo; oral

Drug

matching placebo

Primary outcomes

  1. Assess the efficacy of the study drug (versus placebo) in terms of prebronchodilator forced expiratory volume in 1 second (FEV1).

    Time frame: 6 weeks

Secondary outcomes

  1. Characterize the safety profile of the study drug in terms of adverse events, clinical laboratory tests, vital signs and electrocardiograms.

    Time frame: 6 weeks

  2. Measure the exposure of study drug in terms of plasma concentrations.

    Time frame: 6 weeks

  3. Assess the effect of study drug on asthma control in terms of Asthma Control Questionnaire (ACQ) score, the number of symptom-free days and the number of weekly short-acting beta (ß) 2 agonist (SABA) metered dose inhaler (MDI) actuations.

    Time frame: 6 weeks

  4. Assess the effect of study drug on respiratory function in terms of FEV1, forced vital capacity (FVC), forced expiratory flow (FEF) and peak expiratory flow (PEF).

    Time frame: 6 weeks

Sponsors and collaborators

Lead sponsor

Pfizer

Industry

Registry information

Official study title

A Phase 2 Randomized, Double-blind, Placebo-controlled, Parallel-group, Multicenter Study to Evaluate the Efficacy and Safety of ARRY-502 in Adults With Persistent Asthma

Important dates

Study start
2012
Primary completion
2013
Study completion
2013
First posted
Mar 23, 2012
Registry last updated
Oct 30, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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