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Safety And Efficacy Of Rifabutin In HIV Patients

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Pfizer

Status

Completed

Conditions

Tuberculosis
Inhibition of Disseminated Mycobacterium Avium Complex Disease Associated With HIV Infections
Non-tuberculous Mycobacterial Diseases

Treatments

Drug: rifabutin

Study type

Observational

Funder types

Industry

Identifiers

NCT00810446
A0061007

Details and patient eligibility

About

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 this surveillance, and 3)factors considered to affect the safety and/or efficacy of this drug.

Full description

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

Enrollment

72 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

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

Exclusion criteria

  • Patients not administered Mycobutin®.

Trial design

72 participants in 1 patient group

rifabutin
Description:
Patients administered Rifabutin.
Treatment:
Drug: rifabutin

Trial documents
2

Trial contacts and locations

0

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Data sourced from clinicaltrials.gov

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