Product image of Maviret (Glecaprevir, Pibrentasvir) supplied by GNH India

Maviret

Active Ingredient:
Glecaprevir, Pibrentasvir
Origin:
EU

Maviret (Glecaprevir, Pibrentasvir)

Glecaprevir and Pibrentasvir, the active ingredients in Maviret, are direct‑acting antivirals presented as a 300 mg glecaprevir / 120 mg pibrentasvir tablet for oral use. They treat chronic hepatitis C virus infection (genotypes 1‑6) in adults.

GNH India supplies Maviret as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide.

Manufacturer / TM Owner

Abbvie Deutschland Gmbh & Co. Kg

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Indications & Clinical Uses

Maviret is a direct‑acting antiviral indicated for chronic hepatitis C infection across multiple genotypes.

  • Chronic hepatitis C (genotype 1): achieves sustained virologic response, effectively clearing the virus.
  • Chronic hepatitis C (genotypes 2‑4): achieves sustained virologic response, reducing disease progression.
  • Chronic hepatitis C (genotypes 5‑6): achieves sustained virologic response, improving liver health.

How It Works

  • Glecaprevir inhibits the HCV NS3/4A protease, preventing viral polyprotein processing, while pibrentasvir blocks the NS5A protein, disrupting replication and assembly of hepatitis C virus particles. The combined action halts viral replication, allowing the immune system to clear infected cells.

Side Effects

Common Side Effects

  • Headache: mild to moderate intensity.
  • Fatigue: transient tiredness reported by some patients.
  • Nausea: occasional upset stomach.
  • Diarrhea: loose stools in a minority of users.
  • Abdominal pain: mild discomfort in the upper abdomen.
  • Pruritus: occasional itching.

Serious or Rare Side Effects

  • Elevated liver enzymes: may indicate liver injury.
  • Severe rash or hypersensitivity: requires immediate medical attention.
  • Hepatic decompensation: rare but serious liver failure.
  • Anemia: significant drop in red blood cell count.
  • Jaundice: yellowing of skin or eyes indicating liver dysfunction.
  • Allergic reactions: including swelling of face or throat.

Precautions & Warnings

Before prescribing Maviret, clinicians should consider several safety measures.

  • Baseline liver function assessment: obtain hepatic enzyme levels prior to initiation.
  • Contraindication in moderate/severe hepatic impairment: avoid use in patients with Child‑Pugh B or C.
  • Monitor for drug‑drug interactions: review concomitant medications that affect CYP3A4.
  • Pregnancy safety unknown: use only if potential benefit justifies risk.
  • Breastfeeding caution: insufficient data on excretion in milk.
  • Store at below 25°C: keep in the original packaging, protect from moisture and direct sunlight.

Avoid Interactions

Maviret has notable interactions that require attention.

Major Interactions (Avoid)

  • Strong CYP3A inducers (e.g., rifampin, carbamazepine): may markedly reduce drug exposure.
  • HIV protease inhibitors boosted with ritonavir: can increase exposure and risk of toxicity.
  • St. John’s wort: potent CYP3A inducer that lowers efficacy.

Moderate Interactions (Monitor Closely)

  • Statins (e.g., simvastatin, lovastatin): may increase statin plasma levels, raising risk of myopathy.
  • Antacids containing aluminum or magnesium: can decrease absorption of the tablets.
  • Certain anticonvulsants (e.g., phenytoin): may alter plasma concentrations of the antivirals.

Frequently Asked Questions

Maviret is prescribed for the treatment of chronic hepatitis C virus infection in adults. It is effective across all major HCV genotypes (1 through 6) and is used to achieve a sustained virologic response, which is considered a cure of the infection.

Glecaprevir blocks the HCV NS3/4A protease, preventing the virus from processing its polyprotein, while pibrentasvir inhibits the NS5A protein, disrupting viral replication and assembly. Together they halt the production of new viral particles, allowing the immune system to clear the infection.

The prescribed dose of Maviret is determined by the treating physician based on the patient’s clinical condition, genotype, and liver status. The medication is supplied as a fixed‑dose tablet containing 300 mg glecaprevir and 120 mg pibrentasvir, and the prescriber decides the treatment duration.

The safety of Maviret in pregnancy and lactation has not been established. It should only be used if the potential benefit justifies any possible risk to the fetus or infant, and the decision should be made in consultation with a healthcare professional.

To place an order, submit an enquiry on the product page at gnhindia.com, specifying the required quantity. GNH India supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.

Maviret offers a pan‑genotypic regimen in a single tablet, allowing a short, often 8‑week treatment course for many patients. Compared with older interferon‑based regimens, it provides higher cure rates, fewer side effects, and does not require injections, making it a convenient option for most genotypes.

Maviret tablets should be stored at temperatures below 25 °C, in their original blister pack, protected from moisture and direct sunlight. Do not refrigerate or freeze the tablets, and keep them out of reach of children.

Maviret is taken orally, once daily, with or without food. The tablet should be swallowed whole with a glass of water. Patients should follow the dosing schedule prescribed by their healthcare provider for the full treatment duration.

Serious risks include elevated liver enzymes indicating possible liver injury, severe rash or hypersensitivity reactions, hepatic decompensation in patients with advanced liver disease, and rare cases of anemia. Patients should be monitored regularly for these adverse events.

Maviret is contraindicated in patients with moderate to severe hepatic impairment (Child‑Pugh B or C) and in those receiving strong CYP3A inducers such as rifampin. Caution is also advised for individuals with known hypersensitivity to either component.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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