Mavyret access & copay support
MAVYRET has preferred formulary status on the majority of2:
- State Medicaid Plans
Patients on Medicaid can have out-of-pocket costs of $20 or less depending on state plan.3
- Medicare Part D plans2
- National Commercial Health Plans
Most patients with commercial insurance will pay as little as $5 per month with their MAVYRET copay card.*
Coverage requirements and benefit designs vary by payer and may change over time. Please consult with payers directly for the most current reimbursement policies.
Preferred means the product is placed on the plan’s preferred formulary. Non-preferred products require a higher out-of-pocket cost or step edit, or are placed on a higher tier.
*Terms and Conditions apply.
Find MAVYRET access by state with our formulary lookup tool2
See which plans in your area include MAVYRET on their preferred drug formulary†
Coverage requirements and benefit designs vary by payer and may change over time. Please consult with payers directly for the most current reimbursement policies. The health plans and/or pharmacy benefit managers listed here have not endorsed and are not affiliated with this material.
†Formulary status only includes plans where MAVYRET is available, preferred, or exclusive. Available is defined as on the plan formulary with at least parity positioning to other direct-acting antiviral regimens. Preferred means the product is placed on the plan’s preferred formulary. Non-preferred products require a higher out-of-pocket cost or step edit, or are placed on a higher tier. Exclusive is defined as MAVYRET is the only product in the direct-acting antiviral agents on formulary designated by the insurer.
Save on MAVYRET
Cost should not be a barrier to treatment.
MOST MAVYRET PATIENTS PAY AS LITTLE AS $5 A MONTH5
Terms and Conditions apply. This benefit covers MAVYRET® (glecaprevir and pibrentasvir). Eligibility: Available to patients with commercial prescription insurance coverage for MAVYRET who meet eligibility criteria. Copay assistance program is not available to patients receiving prescription reimbursement under any federal, state, or government-funded insurance programs (for example, Medicare [including Part D], Medicare Advantage, Medigap, Medicaid, TRICARE, Department of Defense, or Veterans Affairs programs) or where prohibited by law or by the patient's health insurance provider. If at any time a patient begins receiving prescription drug coverage under any such federal, state, or government-funded healthcare program, patient will no longer be able to use the MAVYRET copay card and patient must call MAVYRET Patient Support at 1-877-628-9738 and stop use of the copay card. Patients residing in or receiving treatment in certain states may not be eligible. Patients may not seek reimbursement for value received from MAVYRET Patient Support including the copay card from any third-party payers. Offer subject to change or discontinuance without notice. Restrictions, including monthly maximums, may apply. This is not health insurance.
MAVYRET is indicated for the treatment of adult and pediatric patients 3 years and older with chronic hepatitis C virus (HCV) genotype 1, 2, 3, 4, 5, or 6 infection without cirrhosis or with compensated cirrhosis (Child-Pugh A). MAVYRET is indicated for the treatment of adult and pediatric patients 3 years and older with HCV genotype 1 infection, who previously have been treated with a regimen containing an HCV NS5A inhibitor or an NS3/4A protease inhibitor (PI), but not both.
IMPORTANT SAFETY INFORMATION1
WARNING: RISK OF HEPATITIS B VIRUS REACTIVATION IN PATIENTS COINFECTED WITH HCV AND HBV: Test all patients for evidence of current or prior hepatitis B virus (HBV) infection before initiating treatment with MAVYRET. HBV reactivation has been reported in HCV/HBV coinfected patients who were undergoing or had completed treatment with HCV direct-acting antivirals and were not receiving HBV antiviral therapy. Some cases have resulted in fulminant hepatitis, hepatic failure, and death. Monitor HCV/HBV coinfected patients for hepatitis flare or HBV reactivation during HCV treatment and post-treatment follow-up. Initiate appropriate patient management for HBV infection as clinically indicated.
- MAVYRET is contraindicated in patients with moderate or severe hepatic impairment (Child-Pugh B or C) or those with any history of prior hepatic decompensation.
- MAVYRET is contraindicated with atazanavir or rifampin.
WARNINGS AND PRECAUTIONS
Risk of Hepatic Decompensation/Failure in Patients with Evidence of Advanced Liver Disease
- Postmarketing cases of hepatic decompensation/failure, some fatal, have been reported in patients treated with HCV NS3/4A protease inhibitor-containing regimens, including MAVYRET. The median time to onset for MAVYRET was 27 days. The majority had moderate or severe hepatic impairment prior to initiating therapy, including some with compensated cirrhosis at baseline but with a prior decompensation event. Rare cases were reported in patients without cirrhosis or with compensated cirrhosis; many of these patients had evidence of portal hypertension. In patients with compensated cirrhosis or evidence of advanced liver disease, perform hepatic laboratory testing as clinically indicated; and monitor for signs and symptoms of hepatic decompensation such as the presence of jaundice, ascites, hepatic encephalopathy, and variceal hemorrhage. Discontinue MAVYRET in patients who develop evidence of hepatic decompensation/failure.
Risk of Reduced Therapeutic Effect Due to Concomitant Use of MAVYRET with Certain Drugs
- Carbamazepine, efavirenz, and St. John’s Wort may significantly decrease plasma concentrations of glecaprevir and pibrentasvir, leading to reduced therapeutic effect of MAVYRET. The use of these agents with MAVYRET is not recommended.
Most common adverse reactions observed with MAVYRET:
- >10% of subjects: headache and fatigue
- MAVYRET [package insert]. North Chicago, IL: AbbVie Inc.; 2020.
- Data on File. AbbVie Inc. Source: Managed Markets Insight & Technology, LLC MMIT AnalyticsTM as of September 2019, and is subject to change.
- Premium and cost-sharing requirements for selected services for Medicaid adults. Kaiser Family Foundation website. https://www.kff.org/health-reform/state-indicator/premium-and-cost-sharing-requirements-for-selected-services-for-medicaid-expansion-adults. As of January 1, 2020. Accessed June 15, 2020.
- Data on File. AbbVie Inc. IQVIA. National Prescription Audit (NPA), National Prescription Audit Market Dynamics (NPA MD) and Weekly Sales Perspective (WSP) week ending 1/5/2018 to week ending 4/3/2020, Longitudinal Prescription Claims (LRx) week ending 1/5/2018 to week ending 3/27/2020. May 2020. (IQVIA, all rights reserved).
- Data on File. AbbVie Inc. Patient distribution across out-of-pocket filled prescriptions. Based on approved claims data between July 2019-December 2019.
GLOSSARY OF TERMS
AASLD = American Association for the Study of Liver Diseases
APRI = (AST) to platelet ratio index
AUC = area under the curve
BMI = body mass index
CC = compensated cirrhotic
Cure = sustained virologic response (SVR12); HCV RNA <LLOQ at 12 weeks after the end of treatment
DAA = direct-acting antiviral
DCV = daclatasvir
DOD = Department of Defense
F-score = Fibrosis score, F-score restrictions refer to minimum METAVIR fibrosis scores from biopsy (or equivalent quantitative results from approved non-invasive diagnostics such as FibroScan® or FibroTest™) that are required for Medicaid eligibility for HCV treatment. FO = no fibrosis, F1 = portal fibrosis without septa (mild), F2 = portal fibrosis with few septa (moderate), F3 = numerous septa without cirrhosis, F4 = cirrhosis.
FIB-4 = Fibrosis-4
GT = genotype
HBV = hepatitis B virus
HCV = hepatitis C virus
HIV = human immunodeficiency virus
IDSA = Infectious Diseases Society of America
INR = international normalized ratio
ITT = intent-to-treat
KG = kilogram
LLOQ = lower limit of quantification
MAT = medication-assisted treatment
mITT = modified intent-to-treat
NC = non-cirrhotic
NS3/4A = nonstructural proteins 3 and 4A
NS5A = nonstructural protein 5A
PI = protease inhibitor
PP = per-protocol
PPI = proton pump inhibitor
PRS-experienced = prior treatment experience with regimens containing interferon, pegylated interferon, ribavirin, and/or sofosbuvir, but no prior treatment experience with an NS5A inhibitor or HCV NS3/4A protease inhibitor
PS = primary subset
PWID = people who inject drugs
RBV = ribavirin
Relapse = HCV RNA ≥LLOQ after end-of-treatment response among those who completed treatment
RNA = ribonucleic acid
SOF = sofosbuvir
SVR = sustained virologic response
SVR12 = sustained virologic response 12 weeks after the end of treatment
TN = treatment-naïve
VA = Veterans Affairs
FibroTest™ is a trademark of BioPredictive.
S.A.S. FibroScan® is a registered trademark of Echosens™ North America.