Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects

Back to Search
Print
Bookmark Trial

NCT00366652

Last updated date
Back to Search
Print
Bookmark Trial
FOR MORE INFORMATION
Study Location
Neptune, New Jersey, 07753, United States
See other locations
Contact
1-800-718-1021
[email protected]
Related Links

FOR MORE INFORMATION

Contact a representative by phone, email, or visiting the study website. Please see the references below:

By phone

Pfizer Clinical Trials Contact Center

1-800-718-1021

By email

Contact

[email protected]

Call Now

Eligibility Criteria
condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Depression, Depressive Disorder, Major Depressive Disorder
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18-55 years

NEED INFO?

Questions about a trial? Call or email to reach a Pfizer Clinical Trial Contact Center Representative

Pfizer Clinical Trials Contact Center

1-800-718-1021

[email protected]

Call Now

TRY A NEW SEARCH

Search for Clinical Trials by condition, keyword or trial number. Share your location or enter your city or zip code to find studies near you.

Advanced Search

Based on your search, you may also be interested in

Depression, Depressive Disorder, Major Depressive DisorderStudy Evaluating Desvenlafaxine Succinate Sustained Release (DVS SR) Versus Placebo in Peri- and Postmenopausal Women NCT00369343
  1. Birmingham, Alabama
  2. Little Rock, Arkansas
  3. Springdale, Arkansas
  4. Palo Alto, California
  5. San Diego, California
  6. New London, Connecticut
  7. Bradenton, Florida
  8. Miami, Florida
  9. Tampa, Florida
  10. Winter Park, Florida
  11. Atlanta, Georgia
  12. Sandy Springs, Georgia
  13. Savannah, Georgia
  14. Smyrna, Georgia
  15. Idaho Falls, Idaho
  16. Chicago, Illinois
  17. Indianapolis, Indiana
  18. Terre Haute, Indiana
  19. Shreveport, Louisiana
  20. Rockville, Maryland
  21. Omaha, Nebraska
  22. Cherry Hill, New Jersey
  23. Brooklyn, New York
  24. Minot, North Dakota
  25. Beachwood, Ohio
  26. Dayton, Ohio
  27. Toledo, Ohio
  28. Oklahoma City, Oklahoma
  29. Tulsa, Oklahoma
  30. Philadelphia, Pennsylvania
  31. Hilton Head Island, South Carolina
  32. Austin, Texas
  33. Houston, Texas
  34. Richmond, Virginia
  35. Richmond, Virginia
  36. Seattle, Washington
  37. Brown Deer, Wisconsin
Female
40 Years+
years
MULTIPLE SITES
Depression, Depressive Disorder, Major Depressive DisorderStudy Evaluating DVS-233 SR in Adult Outpatients With Major Depressive Disorder NCT00092911
ALL GENDERS
18 Years+
years
MULTIPLE SITES
Depression, Depressive Disorder, Major Depressive DisorderStudy Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects NCT00366652
  1. Neptune, New Jersey
ALL GENDERS
18 Years+
years
MULTIPLE SITES
Advanced Information
Descriptive Information
Brief Title  ICMJE Study Evaluating the Effects of DVS SR and Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
Official Title  ICMJE A Randomized, Open-Label, Crossover, Drug Interaction Study to Evaluate the Effects of DVS SR And Duloxetine on the Pharmacokinetics of Desipramine in Healthy Subjects
Brief Summary The purpose of this study is to evaluate the effects of multiple doses of DVS SR and duloxetine on the pharmacokinetics of a single dose of desipramine in healthy subjects.
Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 3
Study Design  ICMJE Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE
  • Depression
  • Depressive Disorder
  • Depressive Disorder, Major
Intervention  ICMJE
  • Drug: desvenlafaxine SR
  • Drug: desipramine
  • Drug: duloxetine
Study Arms  ICMJE Not Provided
Publications * Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Recruitment Information
Recruitment Status  ICMJE Completed
Estimated Enrollment  ICMJE
 (submitted: August 17, 2006)		20
Original Enrollment  ICMJE Same as current
Study Completion Date  ICMJE September 2006
Primary Completion Date Not Provided
Eligibility Criteria  ICMJE
  1. Healthy men and women between 18 to 55 years of age.
  2. Healthy as determined by the investigator on the basis of medical history and physical examination, laboratory test results, vital signs and a 12-lead electrocardiogram.
  3. History of being a nonsmoker for a least 1 year.
Sex/Gender  ICMJE
Sexes Eligible for Study:All
Ages  ICMJE 18 Years to 55 Years   (Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE United States
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT00366652
Other Study ID Numbers  ICMJE 3151A1-401
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Not Provided
Study Sponsor  ICMJE Wyeth is now a wholly owned subsidiary of Pfizer
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Study Director:Medical MonitorWyeth is now a wholly owned subsidiary of Pfizer
PRS Account Wyeth is now a wholly owned subsidiary of Pfizer
Verification Date May 2007

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP