Status:

COMPLETED

Drug Use Investigation Of Varenicline (Regulatory Post Marketing Commitment Plan)

Lead Sponsor:

Pfizer

Conditions:

Smoking Cessation

Eligibility:

All Genders

Brief Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the LPD (unknown adverse drug reaction), 2) the incidence of adverse drug reactions in thi...

Detailed Description

All the patients whom an investigator prescribes the first Varenicline(Champix) should be registered consecutively until the number of subjects reaches target number in order to extract patients enrol...

Eligibility Criteria

Inclusion

  • Patients need to be administered Varenicline(Champix) in order to be enrolled in the surveillance.

Exclusion

  • Patients not administered Varenicline(Champix).

Key Trial Info

Start Date :

February 1 2009

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

December 1 2012

Estimated Enrollment :

3939 Patients enrolled

Trial Details

Trial ID

NCT00772941

Start Date

February 1 2009

End Date

December 1 2012

Last Update

February 28 2014

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