Last updated: 11/07/2018 18:11:21
A study to compare the pharmacokinetics of a single, oral, 600mg dose of amprenavir in healthy volunteers and patients with cirrhosis.
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 compare the pharmacokinetics of a single, oral, 600mg dose of amprenavir in healthy volunteers and patients with cirrhosis.
Trial description: A study to compare the pharmacokinetics of a single, oral, 600mg dose of amprenavir in healthy volunteers and patients with cirrhosis.
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:
Veronese L, Rautaureau J, Sadler BM, Gillotin C, Petite JP, Pillegand B, Delvaux M, Masliah C, Fosse S, Lou Y, and Stein DS,Single-Dose Pharmacokinetics of Amprenavir, a Human Immunodeficiency Virus Type 1 Protease Inhibitor, in Subjects with Normal or Impaired Hepatic Function. Antimicrob. Agents Chemother. 2000; 44: 821-826.
Veronese L, Rautaureau J, Sadler BM, et al. 1999. A Study To Compare The Pharmacokinetics Of A Single, Oral, 600 Mg Dose Of Amprenavir In Healthy Volunteers And Patients With Cirrhosis PROB1008. Abstracts of the 39th Interscience Conference on Antimicrobial Agents and Chemotherapy: (Abstract #326)
Medical condition
Infection, Human Immunodeficiency Virus
Product
amprenavir
Collaborators
Not applicable
Study date(s)
April 1997 to Invalid Date
Type
Not applicable
Phase
1
Participation criteria
Sex
Not applicable
Age
Not applicable
Accepts healthy volunteers
Not applicable
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
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
Not applicable
Participate in clinical trial
Access to clinical trial data by researchers
Visit website