Retrospective Efficacy and Safety Study With Elbasvir (EBR) 50 mg/Grazoprevir (GZR) 100 mg in Hepatitis C Virus (HCV)-infected Patients With Chronic Kidney Disease (CKD) Stage 4-5 During the French Temporary Authorization for Use (ATU) Program: Data From Real-life
Primary objective : Retrospectively collect and describe the real life efficacy (SVR 12)\* and safety data of EBR 50 mg/GZR 100 mg based therapy, 12 or 16 weeks dosed in HCV-infected patients with chronic kidney disease. These data are collected following French ATU allocation.
Study Type
OBSERVATIONAL
Enrollment
100
Elbasvir 50 mg and grazoprevir 100 mg during the French temporary authorization for use (ATU) program
University Hospital
Caen, France
University Hospital Toulouse
Toulouse, France
Efficacy of Elbasvir (EBR)/Grazoprevir (GZR)
Describe the real life efficacy (Sustained Virologic Response SVR 12) of EBR 50 mg/GZR 100 mg based therapy by assessment of the HCV RNA
Time frame: 12 weeks after the end of all study therapy
Safety during treatment
Assessment of all Adverse Events and laboratory tests collected during treatment
Time frame: during treatment
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