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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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- The HIV Netherlands Australia Thailand Research Collaboration
- Principal Investigator
- Anchalee Avihingsanon, MD, M.DThe HIV Netherlands Australia Thailand Research Collaboration
- Intervention
- LPV/r(drug)
- Enrollment
- 40 enrolled
- Eligibility
- 18-60 years · All sexes
- Timeline
- 2010 – 2015
Study locations (1)
- HIV-NAT Thai Red Cross AIDS Research Center, Bangkok, Thailand
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.
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