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| Sponsor: | Takeda Global Research & Development Center, Inc. |
|---|---|
| Information provided by: | Takeda Global Research & Development Center, Inc. |
| ClinicalTrials.gov Identifier: | NCT00672802 |
Purpose
This purpose of this study is to assess the safety of TAK-375 in subjects with chronic obstructive pulmonary disease.
| Condition | Intervention | Phase |
|---|---|---|
|
Chronic Obstructive Pulmonary Disease COPD |
Drug: TAK-375 and Placebo |
Phase II |
| Study Type: | Interventional |
| Study Design: | Treatment, Randomized, Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Placebo Control, Crossover Assignment, Safety/Efficacy Study |
| Official Title: | A Phase II Safety Study of TAK-375 in Subjects With Mild to Moderate Chronic Obstructive Pulmonary Disease |
| Enrollment: | 26 |
| Study Start Date: | August 2003 |
| Study Completion Date: | March 2004 |
| Primary Completion Date: | March 2004 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
| 1.: Experimental |
Drug: TAK-375 and Placebo
TAK-375 16 mg, tablet, orally, once daily for Periods 1 or 2 and TAK-375 placebo-matching tablets, orally, once daily for Periods 1 or 2.
|
Insomnia is characterized by difficulties initiating and maintaining sleep, or complaints of non-restorative and non-refreshing sleep. Transient insomnia affects approximately one-third to one-half of the US population, based on the results of 2 surveys of representative samples of the adult US population conducted by the Gallup Organization in which respondents were asked if they had "ever had difficulty sleeping." Based on reports of "regular" or "frequent" sleep difficulty, results from the same studies suggest that approximately one-tenth of the US population experiences chronic insomnia. The ideal treatment for insomnia would reduce the latency to onset of sleep and increase total sleep time, without a negative impact on sleep architecture and without safety concerns or next-day effects.
TAK-375 is under global development by Takeda Chemical Industries, Ltd., for the treatment of transient and chronic insomnia and for the treatment of Circadian Rhythm Sleep Disorders.
This study is being conducted to assess the safety of TAK-375 in subjects with chronic obstructive pulmonary disease. Participation in the study is anticipated to be about 1.5 months.
Eligibility| Ages Eligible for Study: | 21 Years and older |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | No |
Inclusion Criteria
Exclusion Criteria:
Any additional condition(s) that in the Investigator's opinion would:
Is required to take or continues taking any disallowed medication, prescription medication, herbal treatment or over-the counter medication, including:
Contacts and Locations| United States, Alabama | |
| Birmingham, Alabama, United States | |
| United States, California | |
| Santa Monica, California, United States | |
| United States, Florida | |
| Winter Park, Florida, United States | |
| Miami Beach, Florida, United States | |
| United States, Kentucky | |
| Louisville, Kentucky, United States | |
| United States, Ohio | |
| Cincinnati, Ohio, United States | |
| Study Director: | VP Clinical Science | Takeda Global Research & Development Center, Inc. |
More Information
| Responsible Party: | Takeda Global Research & Development Center, Inc. ( Sr. VP, Clinical Science ) |
| Study ID Numbers: | 01-03-TL-375-038 |
| Study First Received: | May 2, 2008 |
| Last Updated: | January 26, 2009 |
| ClinicalTrials.gov Identifier: | NCT00672802 History of Changes |
| Health Authority: | United States: Food and Drug Administration |
|
Chronic Obstructive Pulmonary Disease COPD Insomnia Drug Therapy |
|
Lung Diseases, Obstructive Respiratory Tract Diseases Lung Diseases Respiration Disorders Pulmonary Disease, Chronic Obstructive |