Volume 34, Issue 1 pp. 12-21
Clinical Trials and Therapeutic

Efficacy and safety of elbasvir/grazoprevir in participants with hepatitis C virus genotype 1, 4, or 6 infection from the Asia–Pacific region and Russia: Final results from the randomized C-CORAL study

Lai Wei

Corresponding Author

Lai Wei

Peking University Hepatology Institute, Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease, Peking University People's Hospital, Beijing, China

Correspondence

Professor Lai Wei, Peking University Hepatology Institute, Beijing Key Laboratory for Hepatitis C and Immunotherapy for Liver Disease, Peking University People's Hospital, 11 Xizhimen South Street, Beijing 100044, China.

Email: [email protected]

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Ji Dong Jia

Ji Dong Jia

Liver Research Center, Beijing Friendship Hospital, Capital Medical University, Beijing Key Laboratory of Translational Medicine on Cirrhosis, National Clinical Research Center for Digestive Diseases, Capital Medical University, Beijing, China

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Fu Sheng Wang

Fu Sheng Wang

Treatment and Research Center for Infectious Diseases, Beijing 302 Hospital, Beijing, China

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Jun Qi Niu

Jun Qi Niu

Department of Hepatology, First Hospital, Jilin University, Changchun, Jilin, China

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Xu Min Zhao

Xu Min Zhao

Merck Sharp & Dohme, Capital Medical University, Beijing, China

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Shengmei Mu

Shengmei Mu

Merck Sharp & Dohme, Capital Medical University, Beijing, China

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Li Wen Liang

Li Wen Liang

Merck Sharp & Dohme, Capital Medical University, Beijing, China

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Zaiqi Wang

Zaiqi Wang

Merck Sharp & Dohme, Capital Medical University, Beijing, China

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Peggy Hwang

Peggy Hwang

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Michael N Robertson

Michael N Robertson

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Paul Ingravallo

Paul Ingravallo

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Ernest Asante-Appiah

Ernest Asante-Appiah

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Bo Wei

Bo Wei

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Barbara Evans

Barbara Evans

Merck & Co., Inc., Kenilworth, New Jersey, USA

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George J Hanna

George J Hanna

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Rohit Talwani

Rohit Talwani

Merck & Co., Inc., Kenilworth, New Jersey, USA

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Zhong Ping Duan

Zhong Ping Duan

Artificial Liver Center, Beijing YouAn Hospital, Capital Medical University, Beijing, China

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Konstantin Zhdanov

Konstantin Zhdanov

Military Medical Academy n.a. S.M. Kirov, St. Petersburg, Russia

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Pin-Nan Cheng

Pin-Nan Cheng

National Cheng Kung University, Tainan, Taiwan

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Tawesak Tanwandee

Tawesak Tanwandee

Department of Medicine, Faculty of Medicine Siriraj Hospital, Bangkok, Thailand

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Van Kinh Nguyen

Van Kinh Nguyen

National Hospital of Tropical Diseases, Hanoi, Vietnam

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Jeong Heo

Jeong Heo

College of Medicine, Pusan National University and Medical Research Institute, Pusan National University Hospital, Busan, Republic of Korea

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Vasily Isakov

Vasily Isakov

Department of Gastroenterology and Hepatology, Federal Research Center of Nutrition and Biotechnology, Moscow, Russia

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Jacob George

Jacob George

Storr Liver Centre, Westmead Institute for Medical Research, Westmead Hospital and University of Sydney, Westmead, New South Wales, Australia

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on behalf of the C-CORAL Investigators

on behalf of the C-CORAL Investigators

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First published: 12 October 2018
Citations: 16
Declaration of conflict of interest: Lai Wei reports consulting fees from MSD, AbbVie, Bristol-Myers Squibb, Gilead, Allergan, and Johnson & Johnson and grants from AbbVie, Bristol-Myers Squibb, and Roche. Ji Dong Jia reports consulting and lecture fees from AbbVie, Bristol-Myers Squibb, GlaxoSmithKline, Gilead, and MSD. Xu Min Zhao reports personal fees from MSD. Konstantin Zhdanov reports personal fees from MSD, AbbVie, Gilead, Janssen, R-Pharm, and Biocad. Tawesak Tanwandee reports a grant from MSD. Vasily Isakov reports a grant from MSD and personal fees from AbbVie, Bristol-Myers Squibb, Gilead, MSD, and R-Pharm. Shengmei Mu, Li Wen Liang, Peggy Hwang, Ernest Asante-Appiah, Barbara Evans, and Rohit Talwani are employees of MSD. Zaiqi Wang, Michael N. Robertson, Paul Ingravallo, Bo Wei, and George J. Hanna are employees of and report stock ownership in MSD. Jacob George reports other fees from MSD, AbbVie, Bristol-Myers Squibb, and Gilead for advisory board participation. The other authors declare no competing interests.
Author contribution: All authors made substantial contributions to conception and design, acquisition of data, or analysis and interpretation of data; took part in drafting the article or revising it critically for important intellectual content; gave final approval of the version to be published; and agree to be accountable for all aspects of the work. The corresponding author had full access to the data and final responsibility for the decision to submit for publication.
Financial support: The trial was sponsored and funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA, which was responsible for the study design, study management, data collection, and data analysis and was involved in the writing of the report.

Abstract

Background and Aim

Although treatment with direct-acting antivirals has dramatically improved morbidity and mortality attributable to chronic hepatitis C virus infection, universal access to these medicines has been slow in the Asia–Pacific region and Russia. This study evaluated efficacy and safety of elbasvir/grazoprevir in participants with hepatitis C virus infection from Asia–Pacific countries and Russia (C-CORAL).

Methods

C-CORAL was a phase 3, randomized, placebo-controlled study (NCT02251990). Treatment-naive, HIV-negative, cirrhotic and non-cirrhotic participants with chronic hepatitis C genotype 1, 4, or 6 infection were randomized to elbasvir 50 mg/grazoprevir 100 mg once daily for 12 weeks (immediate-treatment group) or placebo followed by deferred treatment with elbasvir/grazoprevir (deferred-treatment group). The primary efficacy outcome was sustained virologic response at 12 weeks, and the primary safety outcome was a comparison between the immediate-treatment group and placebo phase of the deferred-treatment group.

Results

A total of 489 participants were randomized (immediate-treatment group, n = 366; deferred-treatment group, n = 123). Sustained virologic response at 12 weeks in the combined immediate/deferred-treatment groups was 94.4% (459/486; 95% confidence interval = 92.4–96.5%). Sustained virologic response at 12 weeks was 98.2% in participants with genotype 1b, 91.9% with genotype 1a, and 66.7% with genotype 6 infection. Similar rates of adverse events and drug-related adverse events were seen in the immediate-treatment group versus placebo phase of the deferred-treatment group (51.0% vs 50.4% and 21.4% vs 21.1%).

Conclusions

Elbasvir/grazoprevir for 12 weeks represents an effective and well-tolerated treatment option for treatment-naive people with genotype 1 infection from Asia–Pacific countries and Russia.

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