Literature DB >> 27310328

Drug-Drug Interaction of Omeprazole With the HCV Direct-Acting Antiviral Agents Paritaprevir/Ritonavir and Ombitasvir With and Without Dasabuvir.

Akshanth R Polepally1, Sandeep Dutta1, Beibei Hu1, Thomas J Podsadecki1, Walid M Awni1, Rajeev M Menon1.   

Abstract

Paritaprevir (administered with low-dose ritonavir), ombitasvir, and dasabuvir are direct-acting antiviral agents administered as combination regimens for the treatment of chronic hepatitis C virus infection. Drug-drug interactions between 2D (ombitasvir/paritaprevir/ritonavir) or 3D (ombitasvir/paritaprevir/ritonavir and dasabuvir) regimens and omeprazole, a CYP2C19 substrate and acid-reducing agent, were evaluated in 24 healthy volunteers. Subjects received omeprazole (40 mg once daily) on day 1 and days 20-24 and the 2D or 3D regimen (ombitasvir/paritaprevir/ritonavir 25/150/100 mg once daily ± dasabuvir 250 mg twice daily) on days 6-24. Compared with omeprazole alone, coadministration with the 2D or 3D regimen decreased omeprazole geometric mean Cmax and AUCt values by 40% to 50%. Ombitasvir, dasabuvir, and ritonavir mean exposures showed <10% change, and paritaprevir mean exposures showed <20% change when the 2D or 3D regimen was administered with omeprazole compared with administration without omeprazole. Although no a priori dose adjustment is needed, a higher omeprazole dose should be considered if clinically indicated when coadministered with the 2D or 3D regimen. No dose adjustment is required for the 2D or 3D regimen when administered with omeprazole, other acid-reducing agents, or CYP2C19 inhibitors.
© 2016, The American College of Clinical Pharmacology.

Entities:  

Keywords:  CYP2C19; acid-reducing agent; drug-drug interaction; hepatitis C virus; omeprazole

Mesh:

Substances:

Year:  2016        PMID: 27310328     DOI: 10.1002/cpdd.246

Source DB:  PubMed          Journal:  Clin Pharmacol Drug Dev        ISSN: 2160-763X


  12 in total

1.  Paritaprevir and Ritonavir Liver Concentrations in Rats as Assessed by Different Liver Sampling Techniques.

Authors:  Charles S Venuto; Marianthi Markatou; Yvonne Woolwine-Cunningham; Rosemary Furlage; Andrew J Ocque; Robin DiFrancesco; Emily O Dumas; Paul K Wallace; Gene D Morse; Andrew H Talal
Journal:  Antimicrob Agents Chemother       Date:  2017-04-24       Impact factor: 5.191

2.  Exposure-Safety Response Relationship for Ombitasvir, Paritaprevir/Ritonavir, Dasabuvir, and Ribavirin in Patients with Chronic Hepatitis C Virus Genotype 1 Infection: Analysis of Data from Five Phase II and Six Phase III Studies.

Authors:  Chih-Wei Lin; Rajeev Menon; Wei Liu; Thomas Podsadecki; Nancy Shulman; Barbara DaSilva-Tillmann; Walid Awni; Sandeep Dutta
Journal:  Clin Drug Investig       Date:  2017-07       Impact factor: 2.859

3.  Application of Exposure-Response Analyses to Establish the Pharmacodynamic Similarity of a Once-Daily Regimen to an Approved Twice-Daily Dosing Regimen for the Treatment of HCV Infection.

Authors:  Akshanth R Polepally; Haoyu Wang; Patrick J Marroum; Mukul Minocha; Balakrishna Hosmane; Amit Khatri; Sven Mensing; Thomas J Podsadecki; Daniel E Cohen; Walid M Awni; Rajeev M Menon
Journal:  AAPS J       Date:  2017-07-06       Impact factor: 4.009

4.  Pharmacokinetic Evaluation of Darunavir Administered Once or Twice Daily in Combination with Ritonavir or the Three-Direct-Acting Antiviral Regimen of Ombitasvir/Paritaprevir/Ritonavir and Dasabuvir in Adults Coinfected with Hepatitis C and Human Immunodeficiency Viruses.

Authors:  Jennifer R King; Amit Khatri; Roger Trinh; Rolando M Viani; Bifeng Ding; Jiuhong Zha; Rajeev Menon
Journal:  Antimicrob Agents Chemother       Date:  2017-01-24       Impact factor: 5.191

Review 5.  Clinical Pharmacokinetics of Paritaprevir.

Authors:  Rajeev M Menon; Akshanth R Polepally; Amit Khatri; Walid M Awni; Sandeep Dutta
Journal:  Clin Pharmacokinet       Date:  2017-10       Impact factor: 6.447

6.  Population pharmacokinetics of paritaprevir, ombitasvir, dasabuvir, ritonavir and ribavirin in hepatitis C virus genotype 1 infection: analysis of six phase III trials.

Authors:  Sven Mensing; Doerthe Eckert; Shringi Sharma; Akshanth R Polepally; Amit Khatri; Thomas J Podsadecki; Walid M Awni; Rajeev M Menon; Sandeep Dutta
Journal:  Br J Clin Pharmacol       Date:  2016-11-03       Impact factor: 4.335

7.  Pharmacokinetics of Ombitasvir, Paritaprevir, Ritonavir, and Dasabuvir in Healthy Chinese Subjects and HCV GT1b-Infected Chinese, South Korean and Taiwanese Patients.

Authors:  Jiuhong Zha; Bifeng Ding; Haoyu Wang; Weihan Zhao; Chen Yu; Katia Alves; Niloufar Mobashery; Yan Luo; Rajeev M Menon
Journal:  Eur J Drug Metab Pharmacokinet       Date:  2019-02       Impact factor: 2.441

8.  Drug-Drug Interaction between the Direct-Acting Antiviral Regimen of Ombitasvir-Paritaprevir-Ritonavir plus Dasabuvir and the HIV Antiretroviral Agent Dolutegravir or Abacavir plus Lamivudine.

Authors:  Amit Khatri; Roger Trinh; Weihan Zhao; Thomas Podsadecki; Rajeev Menon
Journal:  Antimicrob Agents Chemother       Date:  2016-09-23       Impact factor: 5.191

9.  Dose- and Formulation-Dependent Non-Linear Pharmacokinetic Model of Paritaprevir, a Protease Inhibitor for the Treatment of Hepatitis C Virus Infection: Combined Analysis from 12 Phase I Studies.

Authors:  Akshanth R Polepally; Sven Mensing; Amit Khatri; Denise Beck; Wei Liu; Walid M Awni; Rajeev M Menon; Sandeep Dutta
Journal:  Clin Pharmacokinet       Date:  2016-09       Impact factor: 6.447

10.  Population Pharmacokinetics of Paritaprevir, Ombitasvir, and Ritonavir in Japanese Patients with Hepatitis C Virus Genotype 1b Infection.

Authors:  Sathej M Gopalakrishnan; Akshanth R Polepally; Sven Mensing; Amit Khatri; Rajeev M Menon
Journal:  Clin Pharmacokinet       Date:  2017-01       Impact factor: 6.447

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