NCT Number: NCT00038636
A Study of Two Different Doses of ABT-378/Ritonavir in HIV-Infected Patients Who Have Taken Protease Inhibitors and Non-Nucleoside Reverse Transcriptase Inhibitors
The purpose of this study is to determine the safety and effectiveness of a high dose of ABT-378/ritonavir
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 3
Primary location
Hopital Pitie-Salpetriere, Paris, France
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion:
- HIV positive
- Are at least 18 years old
- Subject has not been treated for an active AIDS-defining opportunistic infection within 15 days of screening
- HIV RNA level > 1000 copies/mL
- Previous therapy with at least one protease inhibitor, at least one non-nucleoside reverse transcriptase inhibitor and at least one nucleoside reverse transcriptase inhibitor
Exclusion:
- Subject is pregnant or breast-feeding
- Subject has received an investigational drug within 30 days prior to screening
- Have a history of pancreatitis
- History of intolerance to ritonavir
- Abnormal laboratory tests at screening
Treatment and study plan
Ritonavir
DrugPrimary outcomes
-
Virologic and immunologic activity evaluations include plasma HIV RNA, CD4 and CD8 cell counts
Sponsors and collaborators
Lead sponsor
Abbott
Industry
Registry information
Important dates
- Study start
- 2000
- First posted
- Jun 4, 2002
- Registry last updated
- Aug 15, 2006
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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