AbbVie Announces European Commission Approval of MAVIRET® (Glecaprevir/Pibrentasvir) for People with Acute Hepatitis C Virus Infection
Rhea-AI Summary
AbbVie (NYSE: ABBV) received European Commission approval for MAVIRET (glecaprevir/pibrentasvir) to treat acute hepatitis C virus (HCV) infection with compensated liver disease, with or without cirrhosis, in adults and children aged 3+ years.
MAVIRET is now the only treatment approved in the EU for both acute and chronic HCV infection. Approval is supported by a Phase 3 study of an eight-week regimen, which showed high efficacy and mainly mild to moderate adverse events such as fatigue, diarrhea, headache and asthenia.
Positive
- European Commission approves MAVIRET for acute HCV in adults and children 3+
- Only treatment approved in EU for both acute and chronic HCV
- Phase 3 eight-week regimen showed high efficacy in acute HCV
- Adverse events in trial were mostly mild or moderate in severity
Negative
- Common adverse events included fatigue, diarrhea, headache and asthenia
News Market Reaction – ABBV
In the Jun 23 session, ABBV gained 2.07%, reflecting a moderate positive market reaction.
Data tracked by StockTitan Argus on the day of publication.
Key Figures
Historical Context
| Date | Event | Sentiment | 24h Move | Catalyst |
|---|---|---|---|---|
| Jun 22 | Acquisition announcement | Positive | +6.6% | Large Apogee acquisition adding late-stage immunology assets and long-term EPS accretion. |
| Jun 16 | FDA approval | Positive | +0.4% | U.S. FDA approval expanding SKINVIVE by JUVÉDERM aesthetic indications in adults. |
| Jun 12 | Clinical data update | Positive | +1.0% | Nine-year CLL14 data showing durable benefits from fixed-duration venetoclax-based regimen. |
| Jun 10 | Consumer insights report | Positive | -0.2% | Aesthetics consumer behavior report without immediate financial or clinical catalysts. |
| Jun 08 | Hematology data presentations | Positive | -0.7% | Broad EHA 2026 blood cancer data across multiple assets and indications. |
24h Move is the share-price change in the day after each event; other market factors may also have contributed.
ABBV often trades in line with positive clinical or deal news, though softer reactions or mild selloffs occur on data-heavy or marketing-focused updates.
Key Terms
pangenotypic medical
direct-acting antiviral medical
cirrhosis medical
end-stage liver disease medical
phase 3 medical
AI-generated analysis. How Rhea-AI works. Not financial advice.
- MAVIRET® (glecaprevir/pibrentasvir) is now approved in the European Union for the treatment of acute hepatitis C virus (HCV) infection with compensated liver disease (with or without cirrhosis) in adults and children aged 3 years and older.
- The approval gives clinicians an option to initiate treatment as soon as acute infection is confirmed, aiming to reduce delays in care and lower the risk of liver disease progression, cirrhosis and liver cancer.
- As the only treatment approved in the EU for both acute and chronic HCV infection, MAVIRET may help streamline care pathways and support broader efforts to advance HCV elimination goals.
"More than 12 million people in
HCV is a highly infectious blood-borne disease that often goes undetected because people may not show symptoms.1 While HCV is curable, many people remain undiagnosed.1 If left untreated, HCV can progress to severe liver complications, including cirrhosis and end-stage liver disease.1 Current clinical guidance supports treating nearly all people with acute or chronic HCV infection.2
"People living with HCV infection frequently face delayed treatment, leading to loss to care and onward transmission," said Massimo Puoti, MD, director of the Infectious Diseases Department at Niguarda Hospital in
Globally, HCV poses a substantial health and economic burden3, with over 200,000 deaths each year from liver cancer.1 People living with HCV are up to 17 times more likely to develop liver cancer than those unaffected.4
The approval was supported by data from the Phase 3, multicenter, single-arm prospective study evaluating the safety and efficacy of MAVIRET eight-week treatment regimen in patients with acute HCV infection.5 The study results showed MAVIRET to be a highly efficacious treatment for people with acute HCV.5 The majority of the adverse events reported were mild or moderate in severity.5 The most common adverse events were fatigue, diarrhea, headache, and asthenia.5
AbbVie continues to collaborate with global regulatory authorities to support access to MAVIRET for people living with acute HCV infection. MAVIRET is approved in
About the Phase 3 M20-350 Study5
The multicenter, single-arm prospective Phase 3 M20-350 clinical trial was designed to evaluate the safety and efficacy of MAVIRET (glecaprevir/pibrentasvir) eight-week treatment in adults and adolescent participants aged 12 years and older with acute HCV infection. The study enrolled 286 treatment-naïve adult patients with acute HCV infection across 70 locations globally. Patients received oral tablets of MAVIRET once daily for eight weeks and were followed for 12 weeks after the end of treatment. The primary endpoint was the percentage of patients with sustained virological response 12 weeks post-treatment (SVR12) in the intent-to-treat population (ITT). The study met its primary endpoint, with
The overall safety profile observed in the M20-350 study was similar to that observed in patients with chronic HCV infection. No serious adverse reactions or adverse reactions leading to treatment discontinuation that were judged as treatment-related were observed among patients with acute HCV infection. The most commonly reported adverse reactions were fatigue (
More information on the study can be found at www.clinicaltrials.gov (NCT04903626).
About MAVIRET® (glecaprevir/pibrentasvir)
MAVIRET® (glecaprevir/pibrentasvir) is an oral, pangenotypic, once-daily, ribavirin-free direct-acting antiviral treatment for acute and chronic hepatitis C virus (HCV) infection in adults and children 3 years and older. MAVIRET combines glecaprevir, an NS3/4A protease inhibitor, and pibrentasvir, an NS5A inhibitor, and is administered once daily with food. In the European Union, MAVIRET is approved for the treatment of acute and chronic HCV infection in adults and children aged 3 years and older.
Important EU Safety Information:
CONTRAINDICATIONS:
MAVIRET is contraindicated in patients with severe hepatic impairment (Child-Pugh C). Concomitant use of MAVIRET is contraindicated with atazanavir-containing products, atorvastatin, simvastatin, dabigatran etexilate, ethinyl oestradiol-containing products, strong P-gp and CYP3A inducers (e.g., rifampicin, carbamazepine,
SPECIAL WARNINGS AND PRECAUTIONS FOR USE:
Hepatitis B virus reactivation
Cases of hepatitis B virus (HBV) reactivation, some of them fatal, have been reported during or after treatment with direct-acting antiviral agents. HBV screening should be performed in all patients before initiation of treatment. HBV/HCV co-infected patients are at risk of HBV reactivation, and should, therefore, be monitored and managed according to current clinical guidelines.
Hepatic impairment
MAVIRET is not recommended in patients with moderate hepatic impairment (Child-Pugh B).
Patients who failed a prior regimen containing an NS5A and/or an NS3/4A inhibitor
MAVIRET is not recommended for the re-treatment of patients with prior exposure to NS3/4A and/or NS5A inhibitors.
Use in diabetic patients
Patients with diabetes may experience improved glucose control and potential symptomatic hypoglycaemia after initiating HCV direct-acting antiviral treatment. Glucose levels should be closely monitored, particularly within the first 3 months of treatment.
ADVERSE REACTIONS
In pooled Phase 2 and 3 clinical studies of adult subjects receiving MAVIRET with genotype 1, 2, 3, 4, 5 or 6 chronic HCV infection the most commonly reported adverse reactions were headache and fatigue.
In a Phase 3b clinical study of adult subjects receiving MAVIRET with genotype 1, 2, 3, or 4 acute HCV infection the most commonly reported adverse reactions were fatigue, asthenia, headache and diarrhoea.
This is not a complete summary of all safety information. See MAVIRET full summary of product characteristics (SmPC) at www.ema.europa.eu.
Globally, prescribing information varies; refer to the individual country product label for complete information.
About AbbVie in Hepatitis C
At AbbVie, our mission begins with putting patients at the center of everything we do. We engage with those affected by hepatitis C (HCV) to understand their needs and work alongside partners and healthcare professionals worldwide to advance solutions and accelerate the elimination of HCV. By raising the standard of care and focusing on closing gaps in the care cascade, we aim for a remarkable impact on patients and transformative change in communities. Every step today brings us closer to global HCV elimination. For more information, visit www.abbvie.com.
About AbbVie
AbbVie's mission is to discover and deliver innovative medicines and solutions that solve serious health issues today and address the medical challenges of tomorrow. We strive to have a remarkable impact on people's lives across several key therapeutic areas including immunology, oncology and neuroscience – and products and services in our Allergan Aesthetics portfolio. For more information about AbbVie, please visit us at www.abbvie.com. Follow @abbvie on LinkedIn, Facebook, Instagram, X, and YouTube.
Forward-Looking Statements
Some statements in this news release are, or may be considered, forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995. The words "believe," "expect," "anticipate," "project" and similar expressions and uses of future or conditional verbs, generally identify forward-looking statements. AbbVie cautions that these forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those expressed or implied in the forward-looking statements. Such risks and uncertainties include, but are not limited to, challenges to intellectual property, competition from other products, difficulties inherent in the research and development process, adverse litigation or government action, changes to laws and regulations applicable to our industry, the impact of global macroeconomic factors, such as economic downturns or uncertainty, international conflict, trade disputes and tariffs, and other uncertainties and risks associated with global business operations. Additional information about the economic, competitive, governmental, technological and other factors that may affect AbbVie's operations is set forth in Item 1A, "Risk Factors," of AbbVie's 2025 Annual Report on Form 10-K, which has been filed with the Securities and Exchange Commission, as updated by its Quarterly Reports on Form 10-Q and in other documents that AbbVie subsequently files with the Securities and Exchange Commission that update, supplement or supersede such information. AbbVie undertakes no obligation, and specifically declines, to release publicly any revisions to forward-looking statements as a result of subsequent events or developments, except as required by law.
Contact(s):
Global Media:
Amber Landis
+1 (231) 557-6596
amber.landis@abbvie.com
Investors:
Liz Shea
liz.shea@abbvie.com
References
1 Hepatitis C. World Health Organization. Available at: https://www.who.int/news-room/fact-sheets/detail/hepatitis-c.
2 European Association for the Study of the Liver, et al. EASL recommendations on treatment of hepatitis C: Final update of the series. J Hepatol. 2020 Nov;73(5):1170-1218.
3 Cacoub P. Comment on Nuño Solinís R, et al. "Value of Treating All Stages of Chronic Hepatitis C: A Comprehensive Review of Clinical and Economic Evidence". Infect Dis Ther. 2017 Jun;6(2):297-301.
4 De Oliveria Andrade LJ., et al. Association between hepatitis C and hepatocellular carcinoma. J Glob Infect Dis. 2009 Jan;1(1):33-7.
5 MAVIRET® Summary of Product Characteristics. AbbVie; 2026.
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SOURCE AbbVie