Seronegatives and Metabolic Abnormalities Protocol 2 (SAMA002): Study to Compare the Effect of Kaletra and Combivir® in HIV-Negative Healthy Subjects

• Status: Completed
• Trial end date: 2006-12-01
• Target enrollment: 0
• Participant gender: All

Summary

This is a randomised study of the effect of treatment with Combivir (zidovudine [AZT] and lamivudine [3TC]) and Kaletra (lopinavir [LPVr]), alone and in combination, on the development of abnormalities in lipid and glucose metabolism in HIV negative healthy subjects.

• Phase: Phase 4
• Accepts Healthy Volunteers?: Accepts Healthy Volunteers

Details

• Lead Sponsor: Kirby Institute
• Collaborators: Garvan Institute of Medical Research; National Heart, Lung, and Blood Institute (NHLBI); Prince of Wales Hospital, Sydney; St Vincent's Hospital, Sydney
• Treatments: Lamivudine; Lamivudine, zidovudine drug combination; Lopinavir; Zidovudine

Criteria

Inclusion Criteria:

• Age >18

• Be able to provide written consent to perform in the trial.

• HIV antibody negative and HIV DNA negative at time of entry to the study.

Exclusion Criteria:

• Any history of, or ongoing, mental or physical condition (including suspected or known diagnosis of ischaemic heart disease), which, in the opinion of the investigator, would impede the subject's ability to participate in the trial.

• History of type I or type II diabetes mellitus or previous treatment with antidiabetic medication.

• Prior use of testosterone, oestrogen, growth hormone or other oral glucocorticoid or anabolic steroid products within the previous six months.

• Alcohol or substance abuse which in the opinion of the investigator would affect the subject's ability to participate in the trial.

• Prior use of anti-retroviral agents (including protease inhibitors, nucleoside or non-nucleoside reverse transcriptase inhibitors, investigational antiretroviral agents or fusion inhibitors either in a previous study, as treatment or as part of post-exposure prophylaxis).

• Prior use of any retinoid-containing compound within the previous six months.

• Abnormal coagulation.

• Previous allergic reaction or known allergy to local anaesthetic.

• Previous use of psychotropic medications.

• Concomitant use of medications, including those metabolised by CYP3A4 enzyme system, which, in the opinion of the investigator, would affect the subject's ability to participate in all activities involved in the trial.

• Any grade-three laboratory abnormality recorded from screening bloods.

• Any grade-two laboratory abnormality recorded from screening bloods, which, in the opinion of the investigator, would impede the subject's ability to safely complete all study requirements.

• Gastrointestinal disorders, which may affect drug absorption.

• Any finding on screening clinical examination, which, in the opinion of the investigator, would impede the subject's ability to participate in the rest of the trial.

• Pregnancy

• Evidence of acute or chronic active hepatitis B virus infection by serology performed at baseline.

• Evidence of hepatitis C infection by serology performed at baseline.