Last updated: 11/07/2018 18:09:44
The Pharmacokinetics and Pharmacodynamics of a Phase I/II Trial to Evaluate the Safety, Pharmacokinetics, and Antiviral Activity of Amprenavir After Multiple Dosing in Subjects With HIV InfectionExtensive searching has revealed that no clinical study report is available for this study…
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: The Pharmacokinetics and Pharmacodynamics of a Phase I/II Trial to Evaluate the Safety, Pharmacokinetics, and Antiviral Activity of Amprenavir After Multiple Dosing in Subjects With HIV InfectionExtensive searching has revealed that no clinical study report is available for this study…
Trial description: The Pharmacokinetics and Pharmacodynamics of a Phase I/II Trial to Evaluate the Safety, Pharmacokinetics, and Antiviral Activity of Amprenavir After Multiple Dosing in Subjects With HIV InfectionExtensive searching has revealed that no clinical study report is available for this study…
Primary purpose:
Not applicable
Trial design:
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Masking:
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Allocation:
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Primary outcomes:
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Secondary outcomes:
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Interventions:
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Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
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Time perspective:
Not applicable
Clinical publications:
Sadler BM, et al. Pharmacokinetic and pharmacodynamic study of the human immunodeficiency virus protease inhibitor amprenavir after multiple oral dosing. Antimicrob Agents Chemother. 2001; 45: 30-37.
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
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Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
Not applicable
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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