Clinical Trials Logo

Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT00671073
Other study ID # GRC-MD-50
Secondary ID
Status Completed
Phase Phase 2
First received
Last updated
Start date May 5, 2008
Est. completion date May 15, 2009

Study information

Verified date September 2019
Source Forest Laboratories
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study will assess the safety and efficacy of a range of oglemilast doses. The study will be 14 weeks in duration. All patients meeting the eligibility criteria will be randomized to one of three doses of oglemilast or placebo.


Recruitment information / eligibility

Status Completed
Enrollment 427
Est. completion date May 15, 2009
Est. primary completion date May 15, 2009
Accepts healthy volunteers No
Gender All
Age group 40 Years to 80 Years
Eligibility Inclusion Criteria:

- Presence of COPD as defined by GOLD criteria (2006); post-bronchodilator FEV1/FVC <70%, and post-bronchodilator FEV1 >30% and < 80% predicted

- Current or former cigarette smoker

Exclusion Criteria:

- Long-term oxygen use of > 15 hours a day

- Symptoms consistent with a significant asthmatic component (e.g. atopic disease, allergic symptoms)

- Any COPD exacerbations within 30 days prior to study entry or during run-in

- History of chronic or recurrent gastrointestinal disorder associated with bleeding in previous 12 months

- Presence of clinical significant pulmonary disease other than COPD

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
Oglemilast
Oglemilast low dose, oral administration, once daily for 12 weeks
Placebo
Placebo, oral administration, once daily for 12 weeks
Oglemilast
Oglemilast middle dose, oral administration, once daily for 12 weeks
Oglemilast
Oglemilast high dose, oral administration, once daily for 12 weeks

Locations

Country Name City State
United States Forest Investigative Site Bethlehem Pennsylvania
United States Forest Investigative Site Birmingham Alabama
United States Forest Investigative Site Buena Park California
United States Forest Investigative Site Centennial Colorado
United States Forest Investigative Site Charleston South Carolina
United States Forest Investigative Site Charlotte North Carolina
United States Forest Investigative Site Cherry Hill New Jersey
United States Forest Investigative Site Cincinnati Ohio
United States Forest Investigative Site Cincinnati Ohio
United States Forest Investigative Site Edina Minnesota
United States Forest Investigative Site El Paso Texas
United States Forest Investigative Site Elmira New York
United States Forest Investigative Site Encinitas California
United States Forest Investigative Site Evansville Indiana
United States Forest Investigative Site Fort Lauderdale Florida
United States Forest Investigative Site Fredericksburg Virginia
United States Forest Investigative Site Fullerton California
United States Forest Investigative Site Greenville South Carolina
United States Forest Investigative Site Livonia Michigan
United States Forest Investigative Site Los Angeles California
United States Forest Investigative Site Medford Oregon
United States Forest Investigative Site Miami Florida
United States Forest Investigative Site Miami Florida
United States Forest Investigative Site Mineola New York
United States Forest Investigative Site Minneapolis Minnesota
United States Forest Investigative Site North Dartmouth Massachusetts
United States Forest Investigative Site Orange California
United States Forest Investigative Site Ormond Beach Florida
United States Forest Investigative Site Papillion Nebraska
United States Forest Investigative Site Philadelphia Pennsylvania
United States Forest Investigative Site Phoenix Arizona
United States Forest Investigative Site Portland Oregon
United States Forest Investigative Site Rancho Mirage California
United States Forest Investigative Site Rochester New York
United States Forest Investigative Site San Antonio Texas
United States Forest Investigative Site San Diego California
United States Forest Investigative Site San Diego California
United States Forest Investigative Site Skokie Illinois
United States Forest Investigative Site Spartanburg South Carolina
United States Forest Investigative Site Stockton California
United States Forest Investigative Site Tacoma Washington
United States Forest Investigative Site Tamarac Florida
United States Forest Investigative Site Toledo Ohio
United States Forest Investigative Site Tucson Arizona
United States Forest Investigative Site Waterbury Connecticut
United States Forest Investigative Site WR1 Wheat Ridge Colorado
United States Forest Investigative Site WR2 Wheat Ridge Colorado

Sponsors (1)

Lead Sponsor Collaborator
Forest Laboratories

Country where clinical trial is conducted

United States, 

Outcome

Type Measure Description Time frame Safety issue
Primary Pre-bronchodilator morning (trough) forced expiratory volume in 1 second (FEV1) After 12 weeks of treatment
Secondary Pre-bronchodilator forced vital capacity (FVC) After 12 weeks of treatment
See also
  Status Clinical Trial Phase
Completed NCT05043428 - The Roles of Peers and Functional Tasks in Enhancing Exercise Training for Adults With COPD N/A
Completed NCT00528996 - An Efficacy and Safety Study to Compare Three Doses of BEA 2180 BR to Tiotropium and Placebo in the Respimat Inhaler. Phase 2
Completed NCT03740373 - A Study to Assess the Pulmonary Distribution of Budesonide, Glycopyrronium and Formoterol Fumarate Phase 1
Completed NCT05402020 - Effectiveness of Tiotropium + Olodaterol Versus Inhaled Corticosteroids (ICS) + Long-acting β2-agonists (LABA) Among COPD Patients in Taiwan
Completed NCT05393245 - Safety of Tiotropium + Olodaterol in Chronic Obstructive Pulmonary Disease (COPD) Patients in Taiwan: a Non-interventional Study Based on the Taiwan National Health Insurance (NHI) Data
Completed NCT04011735 - Re-usable Respimat® Soft MistTM Inhaler Study
Enrolling by invitation NCT03075709 - The Development, Implementation and Evaluation of Clinical Pathways for Chronic Obstructive Pulmonary Disease (COPD) in Saskatchewan
Completed NCT03764163 - Image and Model Based Analysis of Lung Disease Early Phase 1
Completed NCT00515268 - Endotoxin Challenge Study For Healthy Men and Women Phase 1
Completed NCT04085302 - TARA Working Prototype Engagement Evaluation: Feasibility Study N/A
Completed NCT03691324 - Training of Inhalation Technique in Hospitalized Chronic Obstructive Pulmonary Disease (COPD) Patients - a Pilot Study N/A
Completed NCT02236611 - A 12-week Study to Evaluate the Efficacy and Safety of Umeclidinium 62.5 Microgram (mcg) Compared With Glycopyrronium 44 mcg in Subjects With Chronic Obstructive Pulmonary Disease (COPD) Phase 4
Completed NCT00153075 - Flow Rate Effect Respimat Inhaler Versus a Metered Dose Inhaler Using Berodual in Patients With Chronic Obstructive Pulmonary Disease (COPD) Phase 4
Completed NCT01017952 - A Study to Evaluate Annual Rate of Exacerbations and Safety of 3 Dosage Strengths of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD) Phase 3
Completed NCT01009463 - A Study to Evaluate the Efficacy and Safety of Fluticasone Furoate (FF)/GW642444 Inhalation Powder in Subjects With Chronic Obstructive Pulmonary Disease (COPD) Phase 3
Completed NCT04882124 - Study of Effect of CSJ117 on Symptoms, Pharmacodynamics and Safety in Patients With COPD Phase 2
Completed NCT02853123 - Effect of Tiotropium + Olodaterol on Breathlessness in COPD Patients Phase 4
Completed NCT02619357 - Method Validation Study to Explore the Sensitivity of SenseWear Armband Gecko for Measuring Physical Activity in Subjects With Chronic Obstructive Pulmonary Disease (COPD) & Asthma Phase 1
Recruiting NCT05858463 - High Intensity Interval Training and Muscle Adaptations During PR N/A
Not yet recruiting NCT05032898 - Acute Exacerbation of Chronic Obstructive Pulmonary Disease Inpatient Registry Study Stage II