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Trial record 14 of 47 for:    CYCLOBENZAPRINE

To Demonstrate the Relative Bioavailability of Cyclobenzaprine HCl Tablets

The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.
 
ClinicalTrials.gov Identifier: NCT00913419
Recruitment Status : Completed
First Posted : June 4, 2009
Last Update Posted : March 28, 2017
Sponsor:
Information provided by:
Sandoz

Tracking Information
First Submitted Date  ICMJE June 2, 2009
First Posted Date  ICMJE June 4, 2009
Last Update Posted Date March 28, 2017
Study Start Date  ICMJE November 1988
Actual Primary Completion Date December 1988   (Final data collection date for primary outcome measure)
Current Primary Outcome Measures  ICMJE
 (submitted: June 3, 2009)
Bioequivalence based on AUC and Cmax [ Time Frame: 33 days ]
Original Primary Outcome Measures  ICMJE Same as current
Change History Complete list of historical versions of study NCT00913419 on ClinicalTrials.gov Archive Site
Current Secondary Outcome Measures  ICMJE Not Provided
Original Secondary Outcome Measures  ICMJE Not Provided
Current Other Pre-specified Outcome Measures Not Provided
Original Other Pre-specified Outcome Measures Not Provided
 
Descriptive Information
Brief Title  ICMJE To Demonstrate the Relative Bioavailability of Cyclobenzaprine HCl Tablets
Official Title  ICMJE Bioavailability of Cyclobenzaprine HCl Tablets
Brief Summary To demonstrate the relative bioavailability of Cyclobenzaprine HCl tablets.
Detailed Description Not Provided
Study Type  ICMJE Interventional
Study Phase  ICMJE Phase 1
Study Design  ICMJE Allocation: Randomized
Intervention Model: Crossover Assignment
Masking: None (Open Label)
Primary Purpose: Treatment
Condition  ICMJE Depression
Intervention  ICMJE
  • Drug: Cyclobenzaprine HCl Tablets 10 mg, Cord Laboratories
  • Drug: Cyclobenzaprine HCl Tablets 10 mg, Merck Sharp & Dohme
Study Arms  ICMJE
  • Experimental: 1
    Cyclobenzaprine HCl Tablets 10 mg, Cord Laboratories
    Intervention: Drug: Cyclobenzaprine HCl Tablets 10 mg, Cord Laboratories
  • Active Comparator: 2
    Cyclobenzaprine HCl Tablets 10 mg, Merck Sharp & Dohme
    Intervention: Drug: Cyclobenzaprine HCl Tablets 10 mg, Merck Sharp & Dohme
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
Actual Enrollment  ICMJE
 (submitted: June 3, 2009)
30
Original Actual Enrollment  ICMJE Same as current
Actual Study Completion Date  ICMJE December 1988
Actual Primary Completion Date December 1988   (Final data collection date for primary outcome measure)
Eligibility Criteria  ICMJE

Inclusion Criteria:

  • No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening.

Exclusion Criteria:

  • Positive test results for HIV or hepatitis B or C.
  • Treatment for drug or alcohol dependence.
Sex/Gender  ICMJE
Sexes Eligible for Study: Male
Ages  ICMJE 19 Years to 50 Years   (Adult)
Accepts Healthy Volunteers  ICMJE Yes
Contacts  ICMJE Contact information is only displayed when the study is recruiting subjects
Listed Location Countries  ICMJE Not Provided
Removed Location Countries  
 
Administrative Information
NCT Number  ICMJE NCT00913419
Other Study ID Numbers  ICMJE 9038A
Has Data Monitoring Committee Not Provided
U.S. FDA-regulated Product Not Provided
IPD Sharing Statement  ICMJE Not Provided
Responsible Party Eric Mittleberg, Ph.D, VP of Product Development, Sandoz Inc.
Study Sponsor  ICMJE Sandoz
Collaborators  ICMJE Not Provided
Investigators  ICMJE
Principal Investigator: A. Orson Brod, M.D. PharmaKineticsLaboratories, Inc
PRS Account Sandoz
Verification Date June 2009

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