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

Table 17.

Efficacy of 60 mg daclatasvir + 400 mg sofosbuvir QD with or without ribavirin for 12 weeks.

Cirrhosis Prior treatment SVR12 rate
Study and trial phase Ref.
GT-1 GT-2 GT-3
60 mg daclatasvir + 400 mg sofosbuvir QD for 12w
No cirrhosis Naïve 100% (35/35) A1444040, phase 3 Sulkowski et al., 2014a
Naïve 97.3% (73/75) ALLY-3, phase 3 Nelson et al., 2015
Experienced 94.1% (32/34)
Experienced or naive ? ? ANRS CO23 CUPILT Coilly et al., 2016
Naïve 100% (25/25) ANRS/AFEF Hepather Pol et al., 2017
Experienced 97.6% (40/41)
Cirrhosis
Naïve 100% (6/6) AI444040, phase 3 Sulkowski et al., 2014a
Naïve 1a: 83.3% (5/6), 1b: 100% (1/1) ALLY-1, phase 3 Poordad et al., 2016a
Experienced 1a: 100% (7/7), 1b: 100% (2/2)
Naïve 57.9% (11/19) ALLY-3, phase 3 Nelson et al., 2015
Experienced 69.2% (9/13)
Experienced or naive ? ? ANRS CO23 CUPILT Coilly et al., 2016
Naïve 79.5% (31/39) ANRS/AFEF Hepather Pol et al., 2017
Experienced 92.8% (51/55)
Experienced 66.7% (2/3) a 40% (2/5) a Real-world study Cheung et al., 2016

60 mg daclatasvir + 400 mg sofosbuvir QD + ribavirin for 12w
No cirrhosis Naïve 1a:100% (8/8), 1b:100% (1/1) 100% (5/5) ALLY-1, phase 3 Poordad et al., 2016a
Experienced 1a:100% (10/10), 1b:100% (5/5) 83.3% (5/6)
Experienced 100% (2/2) ALLY-3+, phase 3 Leroy et al., 2016
Naïve 100% (4/4)
Naïve ?/36 A1444040, phase 3 Sulkowski et al., 2014a
Naïve 100% (1/1) ANRS/AFEF Hepather Pol et al., 2017
Experienced 100% (8/8)
Naïve 100% (5/5) Real-world study Mangia et al., 2016
Experienced 100% (3/3)
Cirrhosis Naïve 50% (1/2) ALLY-3+, phase 3 Leroy et al., 2016
Experienced 87.5% (14/16)
Naïve 100% (2/2) ANRS/AFEF Hepather Pol et al., 2017
Experienced 91.3% (21/23)
Naïve ?/5 A1444040, phase 3 Sulkowski et al., 2014a
Experienced 88.2% (30/34) a 69.2% (72/104)a Real-world study Cheung et al., 2016

?: Question marks indicate that the data was unavailable.

a

SVR24 rates were used in the study.

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