CompletedPhase 2NCT01138202

Pharmacokinetics (PK) and Safety of 2 Different Doses of Lopinavir/Ritonavir in in HIV/Tuberculosis (TB) Co-infected Patients Receiving Rifampicin Containing Anti-tuberculosis Therapy

Studying Primary genito-urinary tuberculosis

Last synced from ClinicalTrials.gov

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Key facts

Sponsor
The HIV Netherlands Australia Thailand Research Collaboration
Principal Investigator
Anchalee Avihingsanon, MD, M.D
The HIV Netherlands Australia Thailand Research Collaboration
Intervention
LPV/r(drug)
Enrollment
40 enrolled
Eligibility
18-60 years · All sexes
Timeline
20102015

Study locations (1)

Collaborators

Ministry of Health, Thailand

Primary source

Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.

Open NCT01138202 on ClinicalTrials.gov

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