2017
DOI: 10.1056/nejmoa1704053
|View full text |Cite
|
Sign up to set email alerts
|

Glecaprevir and Pibrentasvir in Patients with HCV and Severe Renal Impairment

Abstract: Treatment with glecaprevir and pibrentasvir for 12 weeks resulted in a high rate of sustained virologic response in patients with stage 4 or 5 chronic kidney disease and HCV infection. (Funded by AbbVie; ClinicalTrials.gov number, NCT02651194 .).

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1
1
1
1

Citation Types

22
334
2
7

Year Published

2018
2018
2023
2023

Publication Types

Select...
5
4

Relationship

0
9

Authors

Journals

citations
Cited by 360 publications
(365 citation statements)
references
References 24 publications
22
334
2
7
Order By: Relevance
“…Therefore, sofosbuvir-free treatment options should be preferred if possible. Since the introduction of the pangenotypic combination of glecaprevir/pibrentasvir, a highly effective treatment of GT 2 and 3 is available, and safety and efficacy for patients with renal impairment and hemodialysis have been shown successfully [28]. Alternatively, grazoprevir/elbasvir can be safely administered in patients with GT 1 or 4 infection and severe renal dysfunction [29].…”
Section: Special Groups Of Patientsmentioning
confidence: 99%
“…Therefore, sofosbuvir-free treatment options should be preferred if possible. Since the introduction of the pangenotypic combination of glecaprevir/pibrentasvir, a highly effective treatment of GT 2 and 3 is available, and safety and efficacy for patients with renal impairment and hemodialysis have been shown successfully [28]. Alternatively, grazoprevir/elbasvir can be safely administered in patients with GT 1 or 4 infection and severe renal dysfunction [29].…”
Section: Special Groups Of Patientsmentioning
confidence: 99%
“…In a multicenter phase 3 study, patients with HCV were treated with glecaprevir and pibrentasvir [7]; 88% of the patients were on hemodialysis and 58% were treatment naive, with no previous hepatitis C therapy. The posttreatment results were again in the 95–100% range, with impressively 37% of the patients already at week 1 having no HCV detectable in the blood.…”
Section: Screening and Treating Hepatitis C In Chronic Kidney Diseasementioning
confidence: 99%
“…In a nonrandomized, observational study, the pan-genotypic combination of glecaprevir and pibrentasvir was evaluated in patients with advanced CKD/ESKD (EXPEDITION 4). An SVR12 of 98% was achieved with minimal adverse events (8). The HCV-TARGET (Hepatitis C therapeutic registry and research network) is a realworld outcome study of sofosbuvir-based regimens (5).…”
Section: Treatment Options For Hcv Infection In Patients With Eskdmentioning
confidence: 99%
“…The direct acting antiviral (DAA) agents deliver sustained virologic response rates (undetectable viral load 12 weeks after completion of treatment; SVR12) that routinely exceed 90% after an 8-or 12-week course of therapy. After publication of the pivotal studies completed in the general population (1,4), trials that focused on patients with CKD and ESKD infected with HCV reproduced these excellent results with low adverse event profiles (5)(6)(7)(8). With the availability of safe and effective treatment options for patients with kidney disease, it is important that nephrologists be familiar with the therapeutic possibilities best suited for those with ESKD infected with HCV.…”
Section: Introductionmentioning
confidence: 99%