Combination product
Pronunciation: le-DIP-as-veer and soe-FOS-byoo-veer (har-VOE-nee)
Combination of Ledipasvir and Sofosbuvir.
Each component keeps its own pharmacology page; the combination itself adds no new mechanism.
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| FDA dosing | Population | Start | Target | Max |
|---|---|---|---|---|
| Chronic HCV genotype 1, 4, 5, or 6, without cirrhosis or with compensated cirrhosis | Adults | 1 tablet (90 mg ledipasvir/400 mg sofosbuvir) QD | 12 weeks (8 weeks may be considered in treatment-naive GT1 without cirrhosis, HCV RNA <6 million IU/mL) | Up to 24 weeks (treatment-experienced GT1 with compensated cirrhosis) |
| Chronic HCV GT1 with decompensated cirrhosis, or GT1/4 liver transplant recipients | Adults | 1 tablet QD + ribavirin | 12 weeks | |
| Chronic HCV genotype 1, 4, 5, or 6, without cirrhosis or with compensated cirrhosis | Pediatric 12 yr and older or weighing >=35 kg | 1 tablet QD | 12 weeks | Up to 24 weeks (treatment-experienced with compensated cirrhosis) |
Renal No adjustment for any degree of renal impairment, including ESRD on dialysis
Hepatic No adjustment for mild, moderate, or severe hepatic impairment (Child-Pugh A, B, or C)
Available strengths
Pregnancy No adequate human data. If given with ribavirin, the combination is contraindicated in pregnancy and in male partners of pregnant women.
Lactation Unknown whether components are present in human milk. If given with ribavirin, ribavirin lactation information applies.
| Strength | #/mo | generic $/mo | CostPlus | |
|---|---|---|---|---|
| 45/200 mg | tab | 30 qd | not offered | |
| 90/400 mg | tab | 30 qd | not offered |
Other forms: Ledipasvir (in HARVONI)
Part D rank #922.