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Pharmacokinetic study of rifabutin in HIV-1-positive Japanese individuals

Not Applicable
Conditions
Mycobacteriosis in HIV-positive individuals
Registration Number
JPRN-UMIN000001102
Lead Sponsor
ational Center for Global Health and Medicine
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
Complete: follow-up complete
Sex
All
Target Recruitment
20
Inclusion Criteria

Not provided

Exclusion Criteria

Those who have recieved rifabutine within previous 28 days before study enrollment or who are suspected to have allergy for rifabutin.

Study & Design

Study Type
Observational
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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