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. 2016 Apr 8;32(2):105–109. doi: 10.1159/000445152

Table 2.

Efficacy of (PEG-)IFN-free antiviral therapy in patients with HCV-associated decompensated cirrhosis in controlled, prospective trials

Author Therapy regime Treatment duration, weeks Genotypea n (all) n (MELD > 16) SVR12 (all), n SVR12 (MELD > 16), n
Charlton M, et al. [39]b LDV/SOF + RBV 12–24 1, 4 108d 27 89/108 (82%) ns
Curry MP, et al. [40] SOF/VELc ± RBV 12–24 1, 2, 3, 4, 6 267 12 234/267 (88%) ns
Manns M, et al. [43]b LDV/SOF/RBV 12 1, 4 140 41 121/140 (86%) ns
Poordad F, et al. [42]b LDV/SOF + RBV 12 (–24) 1, 2, 3, 4, 6 60d 13 50/60 (83%) ns
a

Most studies investigated mainly genotype 1.

b

Preliminary results with regard to publication status or completed SVR12.

c

Until November 2015, VEL has not been not approved by the EMA or FDA yet.

d

The complete study included patients prior to and after liver transplantation.

DCV = Daclatasvir; LDV = ledipasvir; RBV = ribavirin; SMV = simeprevir; SOF = sofosbuvir; VEL = velpatasvir; ns = not specified.