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Therefore, the authors recommended that the readers be aware of the limitations pointed out in this report, including the limitations in the design of a multivariate regression study, the test of normality, and be cautious while generalizing or interpreting the findings of this investigation report

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97% achieved an end-of-treatment response and 90% achieved SVR12.[32] Sofosbuvir-Based Treatment in Phase 3 Trials : In a pooled analysis of data from phase 3 trials using sofosbuvir-based regimens, investigators compared HCV treatment responses in participants receiving opioid substitution therapy during treatment (n = 194) with participants not receiving opioid substitution therapy (n = 4,549).[27] There were no significant differences in SVR12 rates (94% in those receiving opioid substitution therapy versus 97% for those not receiving opioid substitution therapy).[27] Sofosbuvir-Velpatasvir (SIMPLIFY) : In this single-arm, open-label, phase 4 study, 103 participants with chronic HCV genotype 1, 2, 3, 4, 5, or 6 infection and recent (within 6 months) injection drug use were treated with a 12-week course of sofosbuvir-velpatasvir.[22] During the treatment course, 59% (61 of 103) participants were receiving opioid substitution therapy, and 74% (76 of 103) had used injection drugs in the month prior to starting treatment.[22] A total of 97% (100 of 103) participants completed treatment

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