Last updated: 11/07/2018 18:08:49
A descriptive study to investigate the pharmacokinetic interaction between amprenavir and ritonavir following their co-administration in subjects with HIV-1 infection.
Clinicaltrials.gov ID
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EudraCT ID
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EU CT Number
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Trial status
Study complete
Study complete
Trial overview
Official title: A descriptive study to investigate the pharmacokinetic interaction between amprenavir and ritonavir following their co-administration in subjects with HIV-1 infection.
Trial description: A descriptive study to investigate the pharmacokinetic interaction between amprenavir and ritonavir following their co-administration in subjects with HIV-1 infection.
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
Cecile Goujard, Isabelle Vincent, Jean-Luc Meynard, Nathalie Choudet, Diane Bollens, Cyril Rousseau et al: Steady-State Pharmacokinetics of Amprenavir Coadministered with Ritonavir in Human Immunodeficiency Virus Type 1-Infected Patients. Antimicrobial Agents and Chemotherapy, January 2003, p. 118-123, Vol. 47, No. 1
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2000-24-05
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
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