Status:

COMPLETED

Safety And Efficacy Of Rescriptor In Patients For Human Immunodeficiency Virus (HIV) Patients

Lead Sponsor:

Pfizer

Conditions:

HIV-1 Infection

Eligibility:

All Genders

Brief Summary

The objective of this surveillance is to collect information about 1) adverse drug reaction not expected from the Local Product Document (LPD) (unlisted adverse drug reaction), 2) the incidence of adv...

Detailed Description

All the patients whom an investigator prescribes the first Rescriptor® should be registered consecutively until the number of subjects reaches target number in order to extract patients enrolled into ...

Eligibility Criteria

Inclusion

  • Patients need to be administered Rescriptor® in order to be enrolled in the surveillance.

Exclusion

  • Patients not administered Rescriptor®.

Key Trial Info

Start Date :

December 1 2003

Trial Type :

OBSERVATIONAL

Allocation :

ACTUAL

End Date :

March 1 2009

Estimated Enrollment :

3 Patients enrolled

Trial Details

Trial ID

NCT00823966

Start Date

December 1 2003

End Date

March 1 2009

Last Update

July 5 2010

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Safety And Efficacy Of Rescriptor In Patients For Human Immunodeficiency Virus (HIV) Patients | DecenTrialz