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. 2017 Feb 24;142:83–122. doi: 10.1016/j.antiviral.2017.02.014

Table 5.

Efficacy of 400 mg sofosbuvir QD + PegIFNα/RBV for 12w.

Cirrhosis Prior treatment SVR12 rate
Study and trial phase Ref.
GT-1 GT-2 GT-3 GT-4 GT-5 GT-6
No cirrhosis
Experienced 100% (9/9) 83.3% (10/12) LONESTAR-2, phase 2 Lawitz et al., 2015b
Naïve 100% (4/4) 100% (7/7) Electron, phase 2a Gane et al., 2013a
Naïve 91.5% (43/47) 93.3% (14/15) 90% (9/10) Phase 2a Lawitz et al., 2013b
Experienced 78.8% (63/80) Phase 2 Pol et al., 2015
Naïve 87% (275/316) 81.8% (9/11) 100% (5/5) ATOMIC, phase 2 Kowdley et al., 2013
Naïve 91.3% (219/240) 100% (27/27) 100% (1/1) 100% (5/5) NEUTRINO, phase 3 Lawitz et al., 2013a
Naïve 95.8% (68/71) BOSON, phase 3 Foster et al., 2015a
Experienced 94.2% (49/52)
Naïve 100% (16/16) ? C-EDGE Head-2-Head,
phase 3
Sperl et al., 2016
Experienced 100% (1/1) ?
Naïve 100% (4/4) HCV-TARGET, phase 4 Feld et al., 2016a
Experienced 75% (3/4)
Naïve 98.1% (252/257) KULDS, real-world study
Ogawa et al., 2016
Experienced 95.9% (95/99)

Cirrhosis Experienced 92.9% (13/14) 83.3% (10/12) LONESTAR-2, phase 2 Lawitz et al., 2015b
Naïve 91.3% (21/23) BOSON, phase 3 Foster et al., 2015a
Experienced 93.8% (15/16) 85.7% (30/35)
Naïve 80.8% (42/52) 0% (0/1) 100% (1/1) NEUTRINO, phase 3 Lawitz et al., 2013a
Naïve 66.7% (2/3) HCV-TARGET, phase 4 Feld et al., 2016a
Experienced 87.5% (7/8)
Naïve 95.6% (43/45) KULDS, real-world study Ogawa et al., 2016
Experienced 82.2% (37/45)

?: Question marks indicate that the data was unavailable in literature.