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One patient, who was lost to follow-up after undergoing randomization to the sofosbuvir-velpatasvir group but before receiving treatment, was excluded from the safety and efficacy analyses

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Students t -test was used when comparing two samples

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Who PT-141 Is For and Who Should Avoid It FDA-approved population (Vyleesi) Vyleesi is approved only for premenopausal women with acquired, generalized HSDD that is not better explained by a medical or psychiatric condition, relationship distress, or medication side effects