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Paroxetine Hydrochloride 40 mg Tablets Under Fed Conditions

This study has been completed.
Sponsor:
Information provided by:
Teva Pharmaceuticals USA
ClinicalTrials.gov Identifier:
NCT00841659
First received: February 9, 2009
Last updated: September 9, 2009
Last verified: September 2009
Results First Received: July 2, 2009  
Study Type: Interventional
Study Design: Allocation: Randomized;   Intervention Model: Crossover Assignment;   Masking: Open Label
Condition: Healthy
Interventions: Drug: Paroxetine HCl
Drug: Paxil®

  Participant Flow
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Recruitment Details
Key information relevant to the recruitment process for the overall study, such as dates of the recruitment period and locations
No text entered.

Pre-Assignment Details
Significant events and approaches for the overall study following participant enrollment, but prior to group assignment
No text entered.

Reporting Groups
  Description
Paroxetine (Test) First Paroxetine HCl 40 mg Tablet (test) dosed in first period followed by Paxil® 40 mg Tablet (reference) dosed in second period
Paxil® (Reference) First Paxil® 40 mg Tablet (reference) dosed in first period followed by Paroxetine HCl 40 mg Tablet (test) dosed in second period

Participant Flow for 3 periods

Period 1:   First Intervention
    Paroxetine (Test) First   Paxil® (Reference) First
STARTED   12   12 
COMPLETED   12   12 
NOT COMPLETED   0   0 

Period 2:   Washout: 2 Weeks
    Paroxetine (Test) First   Paxil® (Reference) First
STARTED   12   12 
COMPLETED   11   12 
NOT COMPLETED   1   0 
Protocol Violation                1                0 

Period 3:   Second Intervention
    Paroxetine (Test) First   Paxil® (Reference) First
STARTED   11   12 
COMPLETED   11   12 
NOT COMPLETED   0   0 



  Baseline Characteristics
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Population Description
Explanation of how the number of participants for analysis was determined. Includes whether analysis was per protocol, intention to treat, or another method. Also provides relevant details such as imputation technique, as appropriate.
No text entered.

Reporting Groups
  Description
Paroxetine (Test) First Paroxetine HCl 40 mg Tablet (test) dosed in first period followed by Paxil® 40 mg Tablet (reference) dosed in second period
Paxil® (Reference) First Paxil® 40 mg Tablet (reference) dosed in first period followed by Paroxetine HCl 40 mg Tablet (test) dosed in second period
Total Total of all reporting groups

Baseline Measures
   Paroxetine (Test) First   Paxil® (Reference) First   Total 
Overall Participants Analyzed 
[Units: Participants]
 12   12   24 
Age 
[Units: Participants]
     
<=18 years   0   0   0 
Between 18 and 65 years   12   12   24 
>=65 years   0   0   0 
Gender 
[Units: Participants]
     
Female   1   2   3 
Male   11   10   21 
Race/Ethnicity, Customized 
[Units: Participants]
     
Caucasian   11   12   23 
Asian   1   0   1 
Region of Enrollment 
[Units: Participants]
     
Canada   12   12   24 


  Outcome Measures
  Show All Outcome Measures

1.  Primary:   Cmax - Maximum Observed Concentration (of Paroxetine in Plasma)   [ Time Frame: Blood samples collected over 120 hour period ]

2.  Primary:   AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated)   [ Time Frame: Blood samples collected over 120 hour period ]

3.  Primary:   AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant)   [ Time Frame: Blood samples collected over 120 hour period ]


  Serious Adverse Events


  Other Adverse Events


  Limitations and Caveats
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Limitations of the study, such as early termination leading to small numbers of participants analyzed and technical problems with measurement leading to unreliable or uninterpretable data
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  More Information
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Certain Agreements:  
Principal Investigators are NOT employed by the organization sponsoring the study.
There IS an agreement between Principal Investigators and the Sponsor (or its agents) that restricts the PI's rights to discuss or publish trial results after the trial is completed.
The agreement is:
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is less than or equal to 60 days. The sponsor cannot require changes to the communication and cannot extend the embargo.
unchecked The only disclosure restriction on the PI is that the sponsor can review results communications prior to public release and can embargo communications regarding trial results for a period that is more than 60 days but less than or equal to 180 days. The sponsor cannot require changes to the communication and cannot extend the embargo.


Results Point of Contact:  
Name/Title: Manager, Biopharmaceutics
Organization: Teva Pharmaceuticals USA
phone: 1-866-384-5525
e-mail: clinicaltrialqueries@tevausa.com



ClinicalTrials.gov Identifier: NCT00841659     History of Changes
Other Study ID Numbers: 02183-A
Study First Received: February 9, 2009
Results First Received: July 2, 2009
Last Updated: September 9, 2009