Combination product
Pronunciation: glek-A-pre-veer and pi-BRENT-as-veer (MAV-i-ret)
Combination of Glecaprevir and Pibrentasvir.
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 or acute HCV genotype 1–6 (without cirrhosis or with compensated cirrhosis, Child-Pugh A) | Adults and pediatric patients ≥12 years or weighing ≥45 kg | 3 tablets (glecaprevir 300 mg/pibrentasvir 120 mg) QD with food | Treatment duration 8–16 weeks based on genotype, cirrhosis, and prior treatment | 300 mg/120 mg per day |
| Chronic or acute HCV genotype 1–6 (without cirrhosis or with compensated cirrhosis, Child-Pugh A) | Pediatric patients 3 to <12 years (<45 kg) | Weight-based oral pellets QD with food: <20 kg = 150/60 mg; 20–<30 kg = 200/80 mg; 30–<45 kg = 250/100 mg | Treatment duration 8–16 weeks based on genotype, cirrhosis, and prior treatment | 250 mg/100 mg per day (30–<45 kg) |
Renal No adjustment needed
Hepatic No adjustment for mild (Child-Pugh A); contraindicated in moderate or severe (Child-Pugh B or C) or any history of prior hepatic decompensation
Take with food; treatment duration is 8–16 weeks based on genotype, cirrhosis status, and prior treatment experience.
Available strengths
Pregnancy No adequate human data; animal reproduction studies showed no adverse developmental effects (glecaprevir rabbit exposures limited).
Lactation Unknown whether excreted in human milk; components present in rodent milk without observed effects on nursing pups.
| Strength | #/mo | generic $ | brand $ | CostPlus | |
|---|---|---|---|---|---|
| 100/40 mg | tab | 30 qd | — | $4,589.50/mo | not offered |
| 50/20 mg | pellet | per unit | — | not offered |
Other forms: Glecaprevir (MAVYRET)
Part D rank #714.