Last updated: 11/07/2018 18:08:39
A Study to Further Investigate the Degree of Pharmacokinetic Interaction Between Amprenavir and Ritonavir Following Their Co-Administration to Healthy Subjects.
Clinicaltrials.gov ID
Not applicable
EudraCT ID
Not applicable
EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: A Study to Further Investigate the Degree of Pharmacokinetic Interaction Between Amprenavir and Ritonavir Following Their Co-Administration to Healthy Subjects.
Trial description: A Study to Further Investigate the Degree of Pharmacokinetic Interaction Between Amprenavir and Ritonavir Following Their Co-Administration to Healthy Subjects.
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:
Sadler B.M., Piliero P.J., Preston S.L., Lloyd P.P., Lou Y., Stein D. Pharmacokinetics and safety of amprenavir and ritonavir following multiple-dose, co-administration to healthy volunteers. AIDS. 2001; 15: 1009-1018..
Sale M, Sadler B.M., Stein D.S. Pharmacokinetic modeling and simulations of interaction of amprenavir and ritonavir. Antimicrob Agents Chemother. 2002; 46: 746-754.
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
1999-06-12
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
Not applicable
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