Effect of Tenofovir Disoproxil Fumarate on the Pharmacokinetics and Pharmacodynamics of Total, R‐, and S‐Methadone
- 1 August 2004
- journal article
- clinical trial
- Published by Wiley in Pharmacotherapy: The Journal of Human Pharmacology and Drug Therapy
- Vol. 24 (8) , 970-977
- https://doi.org/10.1592/phco.24.11.970.36141
Abstract
Study Objective. To evaluate the potential effect of tenofovir disoproxil fumarate (DF) on the pharmacokinetics of methadone.Design. Phase I, open‐label, fixed‐sequence, pharmacokinetic drug‐drug interaction study.Setting. Clinical research center.Subjects. Fourteen volunteers receiving stable methadone maintenance therapy who were not infected with the human immunodeficiency virus.Intervention. Tenofovir DF was added to the subjects' methadone regimens.Measurements and Main Results. The pharmacokinetics of total, R‐, and S‐methadone were evaluated at baseline and after 2 weeks of daily tenofovir DF coadministration with a light meal. Steady‐state tenofovir DF pharmacokinetics were evaluated at day 15. Bioequivalence testing was conducted of total, R‐, and S‐methadone area under the serum or plasma concentration‐time curve during the 24‐hour dosing interval at steady state (AUCss) and maximum concentration in serum or plasma (Cmax). Subjects were evaluated for changes in methadone pharmacodynamics by the Short Opiate Withdrawal Scale (SOWS) and pupillary diameter measurements at frequent intervals. Coadministration with tenofovir DF did not affect the pharmacokinetics of methadone. Geometric mean R‐methadone systemic exposures, AUCss and Cmax, differed by 5% or less when methadone was dosed with tenofovir D F. Similar results were observed for S‐methadone and for total methadone. Both AUCss and Cmax met the strict criteria for bioequivalence between the two study periods for total, R‐, and S‐methadone, indicating a lack of drug interaction when tenofovir DF was coadministered with methadone. No significant changes in SOWS scores or pupillary diameter measurements occurred, and no notable clinical adverse events were reported.Conclusion. Tenofovir DF pharmacokinetics were comparable to previously reported values of tenofovir DF in HIV‐infected patients. Coadministration of methadone with tenofovir DF did not alter the pharmacokinetics or pharmacodynamics of total, R‐, or S‐methadone. Tenofovir DF may be given as part of a once‐daily antiretroviral regimen in patients receiving methadone maintenance therapy.Keywords
This publication has 28 references indexed in Scilit:
- Absence of Opioid Withdrawal Symptoms in Patients Receiving Methadone and the Protease Inhibitor Lopinavir‐RitonavirClinical Infectious Diseases, 2002
- Pharmacokinetics of methadone in HIV-positive patients receiving the non-nucleoside reverse transcriptase efavirenzPublished by Wiley ,2002
- Pharmacokinetic Interactions of Nevirapine and Methadone and Guidelines for Use of Nevirapine to Treat Injection Drug UsersClinical Infectious Diseases, 2001
- Phase I/II Trial of the Pharmacokinetics, Safety, and Antiretroviral Activity of Tenofovir Disoproxil Fumarate in Human Immunodeficiency Virus-Infected AdultsAntimicrobial Agents and Chemotherapy, 2001
- The pharmacokinetics of methadone in HIV‐positive patients receiving the non‐nucleoside reverse transcriptase inhibitor efavirenzBritish Journal of Clinical Pharmacology, 2001
- Interaction of Methadone with Didanosine and StavudineJAIDS Journal of Acquired Immune Deficiency Syndromes, 2000
- Interaction of methadone with substrates of human hepatic cytochrome P450 3A4Toxicology, 1997
- Fluoxetine Addition to Methadone in Addicts: Pharmacokinetic AspectsTherapeutic Drug Monitoring, 1996
- Involvement of Cytochrome P450 3A4 Enzyme in the N-Demethylation of Methadone in Human Liver MicrosomesChemical Research in Toxicology, 1996
- Inhibition of human cytochrome P450 2D6 (CYP2D6) by methadone.British Journal of Clinical Pharmacology, 1993