Real-World Safety and Effectiveness of an 8-Week Regimen of Glecaprevir/Pibrentasvir in Patients with Hepatitis C and Cirrhosis

Author:

Lu Mei,Rupp Loralee B.,Melkonian Christina,Trudeau Sheri,Daida Yihe G.,Schmidt Mark A.,Gordon Stuart C.

Funder

AbbVie

Publisher

Springer Science and Business Media LLC

Subject

Pharmacology (medical),General Medicine

Reference14 articles.

1. Lampertico P, Carrion JA, Curry M, et al. Real-world effectiveness and safety of glecaprevir/pibrentasvir for the treatment of patients with chronic HCV infection: a meta-analysis. J Hepatol. 2020;72(6):1112–21.

2. US Food and Drug Administration. Mavret Summary Review. https://www.accessdata.fda.gov/drugsatfda_docs/nda/2017/209394Orig1s000SumR.pdf. Accessed 1 May 2023.

3. US Food and Drug Administration. Mavret: Label for New Patient Population. https://www.accessdata.fda.gov/drugsatfda_docs/label/2019/209394s006lbl.pdf. Accessed May 1, 2023.

4. Brown RS Jr, Buti M, Rodrigues L, et al. Glecaprevir/pibrentasvir for 8 weeks in treatment-naive patients with chronic HCV genotypes 1–6 and compensated cirrhosis: the EXPEDITION-8 trial. J Hepatol. 2020;72(3):441–9.

5. US Food and Drug Administration. Mavyret Labeling Information. https://www.accessdata.fda.gov/drugsatfda_docs/label/2020/209394s010lbl.pdf. Published 2020. Accessed 2023.

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