Pharmacokinetic Study of Oseltamivir and Intravenous Zanamivir in Healthy Adults

It is very likely that during an influenza pandemic, intravenous zanamivir will be used in combination with oseltamivir. Although the potential for a drug interaction between the two drugs is very low, the likelihood of coadministration combined with the common route of renal clearance of both drugs and the current lack of information on the organic anion transporter polypeptides (OATP) inhibition potential of zanamivir in vivo warrants verification of a lack of an interaction. This study will provide clinical guidance for the use of intravenous zanamivir in settings where oral oseltamivir is commonly used, such as areas in which human cases of H5N1 have been reported.

The total duration of study participation is approximately 13 weeks. Each participant will have a screening visit, four treatment steps, and a follow-up visit. The screening visit to determine enrollment eligibility will be conducted within 45 days prior to receiving the first dose. Participants will be randomized to receive either Regimen A or B for Step 1. Participants who received Regimen A will receive Regimen B in Step 2 and vice versa. After completing Step 2, all participants will continue with Regimens C and D, consecutively, in Steps 3 and 4, with at least 3 days between each step. A follow-up visit will occur 7-10 days after completing the last treatment assessments or withdrawing from the study.

Regimen A consists of continuous intravenous zanamivir infusion (800 mg) for 16 hours. Regimen B consists of 150 mg oral oseltamivir tablets taken five times over 3 days. Regimen C consists of 150 mg oral oseltamivir tablets taken five times over 3 days plus continuous intravenous zanamivir infusion (3600 mg) for 36 hours. Regimen D consists of 150 mg oral oseltamivir tablets taken five times over 3 days plus intermittent intravenous zanamivir infusion received in five 30 minute intervals (3000 mg total).

Blood and urine collection, vital signs, pharmacokinetic sampling, adverse event assessment, and pregnancy test for females will occur at each step in the study. The follow-up visit will involve blood and urine collection, vital signs, adverse event assessment, and pregnancy test for females.

Inclusion criteria

• Good general health
• Body mass index between 17 - 32 kg/m^2
• Body weight of at least 37 kg
• Able to read, comprehend, and write at a sufficient level to complete study-related materials
• Normal ECG with QTC less than 450 msec as judged by cardiologist
• Willing and ability to comply with the study protocol for the duration of the trial

Exclusion criteria

• History of cardiac disease or abnormality. More information on this criterion can be found in the protocol.
• Family history of sudden cardiac death
• HIV-infected
• Hepatitis C virus infected
• Positive for hepatitis B surface antigen (HBsAg)
• History of renal disease, hepatic disease, and/or cholecystectomy
• Evidence of active substance abuse
• History of alcohol or substance abuse or dependence within 6 months prior to study entry. More information on this criterion can be found in the protocol.
• Use of prescription or non-prescription drugs, except paracetamol, at doses of up to 2 g/day. More information on this criterion can be found in the protocol.
• Use of FluMist, inactivated influenza vaccine, or any other anti-influenza antiviral medications within 14 days prior to study entry
• Participated in a clinical trial and received a drug or new chemical entity within 30 days or five half-lives prior to study entry.
• Unwilling to abstain from ingesting alcohol within 48 hours prior to study entry until collection of the final pharmacokinetic sample during each period
• Donated blood to the extent that participation in this study would result in excess of 300 mL donated within a 30 day period
• History of allergy to the study drug or drugs of this class. More information on this criterion can be found in the protocol.
• Unstable medical condition that, in the opinion of the investigator, would interfere with the study
• Anyone that, in the opinion of the investigator, has a risk of non-compliance with study procedures
• AST or ALN of at least 1.5 ULN
• Certain abnormal laboratory values
• Agree to use effective methods of birth control. More information on this criterion can be found in the protocol.
• Pregnant or breastfeeding