NCT Number: NCT00002372
A Study of 141W94 in Combination With Other Anti-HIV Drugs
To determine the steady-state pharmacokinetics of 141W94 in combination with saquinavir, indinavir and nelfinavir after multiple oral dosing. To determine the steady-state pharmacokinetics of saquinavir, indinavir, and nelfinavir in combination with 141W94 after multiple oral dosing. To assess the safety and tolerability of multiple doses of 141W94 when combined with saquinavir, indinavir and nelfinavir.
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Notify MeKey information
Conditions
Age range
18 year and older
Sex eligibility
All sexes
Study type
Interventional
Phase
Phase 1
Primary location
Univ of California / San Diego Treatment Ctr, San Diego, California, United States
About this study
Patients will be randomized to receive open label 141W94 in combination with saquinavir, indinavir and nelfinavir. The randomized phase will be preceded by a single dose pharmacokinetic interaction study of 141W94 and indinavir in 12 patients. Data from this single dose investigation will be used to determine the dose of indinavir to be used in the randomized phase.
Who can participate
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Concurrent Medication:
Allowed provided used with caution:
Medications that may interact at CYP3A4 (either a substrate, inhibitor or inducer of the enzyme) should be used with caution.
Patients must have:
- Documented HIV infection.
- CD4+ cell count >= 200 cells/mm3.
- Anticipated need for treatment with cytotoxic chemotherapeutic agents within the study time period.
- Treatment with immunomodulating agents.
- Medications that should not be administered with 141W94:
Terfenadine. Astemizole. Cisapride. Triazolam. Midazolam. Ergotamine/Dihydroergotamine-containing regimens. Antiretroviral drugs. Vitamin E supplements. Other experimental agents.
Anticipated need for radiation therapy within the study time period.
- Prior protease inhibitors.
- Antiretroviral therapy within 2 weeks prior to entry.
- Treatment with cytotoxic chemotherapeutic agents within 4 weeks prior to entry.
Radiation therapy within 4 weeks prior to entry. Current alcohol or illicit drug use that, in the opinion of the investigator, may interfere with the patient's ability to comply with the dosing and protocol evaluations.
Treatment and study plan
Amprenavir
Drugnelfinavir mesylate
DrugSaquinavir
DrugSponsors and collaborators
Lead sponsor
Glaxo Wellcome
Industry
Registry information
Official study title
A Phase I/II Screening Trial to Identify Potential Partner Compounds to Use in Combination With 141W94
Important dates
- First posted
- Aug 31, 2001
- Registry last updated
- Jun 24, 2005
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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