Mavyret
Named-patient access overview. Mavyret is coordinated by Reserve Meds for international patients via physician-led cross-border sourcing.
Quick orientation
Mavyret (glecaprevir / pibrentasvir) is an oral pangenotypic fixed-dose combination direct-acting antiviral developed by AbbVie that pairs an NS3/4A protease inhibitor with an NS5A inhibitor. The US Food and Drug Administration approved Mavyret in August 2017 for the treatment of chronic hepatitis C virus infection in adults and, after a 2021 pediatric expansion, in patients three years and older across all six major HCV genotypes. The drug is given as three oral tablets once daily with food, for an 8-week course in treatment-naive patients without cirrhosis and 12 to 16 weeks in select treatment-experienced or compensated-cirrhotic populations. Mavyret is prescribed and monitored by hepatology, gastroenterology, or infectious-disease specialists in outpatient liver-clinic settings.
Case active and ready to skip the regulatory walkthrough? Start your case or WhatsApp us.
How Reserve Meds coordinates Mavyret
- Patient or treating physician submits an intake at the patient portal.
- Reserve Meds clinical team verifies appropriateness for the patient and destination country.
- Treating physician issues prescription and clinical justification.
- Country-specific named-patient documentation is prepared.
- Mavyret is sourced from a DSCSA-compliant US specialty wholesaler with full serial traceability.
- Shipment is coordinated to the patient's physician or hospital pharmacy with appropriate handling.
Access by country
Reserve Meds publishes a detailed country access guide for Mavyret in every market we coordinate. Each page below covers the destination-country regulatory pathway, real costs, indicative timelines, physician-credential requirements, and handling notes. Tap any country to read the full deep-dive.
Start a request for Mavyret
Submit a 60-second intake. The clinical team will follow up within 24 hours with case-specific feasibility, timeline, and a formal quote.
Frequently asked questions
How can I get Mavyret if it is not approved or available in my country?
Reserve Meds coordinates US-sourced Mavyret for patients through a physician-led, named-patient cross-border pathway. Your treating physician provides the prescription and clinical justification; Reserve Meds prepares the named-patient documentation for your country and arranges DSCSA-compliant US sourcing and delivery to your physician or hospital pharmacy.
Can I access Mavyret through named-patient or compassionate-use import?
Yes. Named-patient access (also called compassionate use or personal import) is the core route Reserve Meds operates for Mavyret. Eligibility and paperwork depend on the regulator in your country, and Reserve Meds maps the specific pathway for each market it coordinates.
Do I need a prescription to access Mavyret through Reserve Meds?
Yes. Reserve Meds is not a pharmacy and does not prescribe. A valid prescription and clinical justification from your treating physician are required, and all clinical decisions remain with your physician.
How does Reserve Meds deliver Mavyret to a patient?
Reserve Meds sources Mavyret from a DSCSA-compliant US specialty supplier with full traceability and coordinates delivery to your treating physician or hospital pharmacy, with appropriate handling for the product.
How long does it take, and what does Mavyret cost through Reserve Meds?
After a short intake, the clinical team responds within one business day with case-specific feasibility, an indicative timeline, and a formal written quote. Cost depends on the destination, the prescribed regimen, and the duration of therapy, and is confirmed in writing before anything proceeds.
How do I start a request for Mavyret?
Submit a 60-second intake through the Reserve Meds patient portal, or message the concierge team on WhatsApp. A named coordinator follows up within 24 hours.