GNH USA

Europe — EMA

Mektovi

GNH USA supplies Mektovi (Binimetinib), a MEK inhibitor for melanoma and non‑small cell lung cancer. Request a quote for global supply and pricing.

Binimetinib

Request sourcing

1
Pack/s

What is Binimetinib?

Binimetinib, the active ingredient in Mektovi, is a MEK inhibitor presented as an oral tablet for oral use. It is used to treat certain advanced melanomas and non‑small cell lung cancers in adult patients. GNH USA supplies Mektovi as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, oncology centres, pharmacies and clinics worldwide.

What is Binimetinib used for?

Mektovi targets the MAPK/ERK signaling pathway, which is frequently dysregulated in solid tumours. - Melanoma: helps control disease progression in patients with BRAF‑mutated advanced melanoma. - Non‑small cell lung cancer: used in combination therapy to improve outcomes in patients with KRAS‑mutated NSCLC.

What are the side effects of Binimetinib?

Adverse reactions may occur with any antineoplastic therapy.

Common Side Effects: - Diarrhea: frequent loose stools that may require supportive care. - Rash: skin eruptions ranging from mild to moderate severity. - Nausea: feeling of sickness often managed with anti‑emetics. - Fatigue: persistent tiredness affecting daily activities.

Serious or Rare Side Effects: - Interstitial lung disease: inflammation of lung tissue that can be life‑threatening. - Cardiac dysfunction: reduced left‑ventricular ejection fraction or heart failure. - Retinal disorders: visual disturbances including serous retinal detachment. - Severe hypertension: markedly elevated blood pressure requiring immediate treatment. - Hepatic toxicity: significant elevation of liver enzymes or liver failure. - Febrile neutropenia: fever with low neutrophil count, increasing infection risk.

What precautions apply to Binimetinib?

Patients should be monitored closely for safety concerns before and during treatment. - Cardiac monitoring: assess baseline and periodic ejection fraction. - Liver function: check transaminases and bilirubin regularly. - Ocular assessment: perform baseline eye exam and monitor for visual changes. - Renal impairment: evaluate kidney function and adjust use if severe. - Contraception: advise effective birth control during therapy and for a defined period after discontinuation. - Store at room temperature: keep in the original packaging, protect from moisture and direct sunlight.

What does Binimetinib interact with?

Binimetinib may interact with other medicines, altering efficacy or safety.

Major Interactions (Avoid): - Strong CYP3A4 inducers (e.g., rifampin, carbamazepine): may reduce exposure. - Strong CYP3A4 inhibitors (e.g., ketoconazole, clarithromycin): may increase exposure. - QT‑prolonging agents: combined use can heighten risk of cardiac arrhythmia.

Moderate Interactions (Monitor Closely): - Antacids containing aluminum or magnesium: may affect absorption; separate dosing. - Warfarin: monitor INR as binimetinib can influence anticoagulant effect.

Frequently asked questions

What conditions is Mektovi used to treat?+
Mektovi, containing the active ingredient binimetinib, is prescribed for adult patients with advanced melanoma that carries a BRAF mutation and for certain non‑small cell lung cancers, particularly those with KRAS mutations, as part of a targeted therapy regimen.
How does binimetinib work in the body?+
Binimetinib blocks the activity of MEK1 and MEK2 enzymes within the MAPK/ERK signaling pathway. By inhibiting these kinases, it prevents downstream phosphorylation events that drive cancer cell growth and survival, thereby slowing tumor progression.
What is the usual dose of Mektovi?+
The specific dose and schedule of Mektovi are determined by the prescribing oncologist based on the patient’s clinical condition, disease characteristics, and any concomitant therapies. Dosing information is provided in the product’s prescribing information.
Is Mektovi safe to use during pregnancy or breastfeeding?+
The safety of binimetinib in pregnancy or while nursing has not been established. Women of childbearing potential should use effective contraception during treatment and for a defined period after the last dose. Breastfeeding is generally not recommended.
How do I order Mektovi from GNH USA?+
To request Mektovi, submit an enquiry on the product page at gnh-usa.com specifying the required quantity. GNH USA works with hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any necessary import documentation.
How does Mektovi compare with other MEK inhibitors?+
Mektovi (binimetinib) is one of several MEK inhibitors approved for oncology use. Compared with alternatives such as trametinib, binimetinib has a distinct pharmacokinetic profile and may be selected based on specific mutation status, combination regimen, and tolerability considerations evaluated by the treating physician.
What are the storage requirements for Mektovi?+
Mektovi tablets should be stored at room temperature, below 25 °C, in the original container to protect them from moisture and light. Do not store in a bathroom or other humid environment.
How is Mektovi administered?+
Mektovi is taken orally, usually once daily, with or without food as directed by the prescriber. The tablets should be swallowed whole with a glass of water and not crushed or chewed.
What are the most serious risks associated with Mektovi?+
Serious adverse events linked to Mektovi include interstitial lung disease, cardiac dysfunction (such as reduced ejection fraction), retinal disorders, severe hypertension, hepatic toxicity, and febrile neutropenia. Patients should be monitored regularly for these conditions and report any new symptoms promptly.
Who should not use Mektovi?+
Mektovi is contraindicated in patients with known hypersensitivity to binimetinib or any of its excipients. It should be used with caution, or avoided, in individuals with significant cardiac, hepatic, or renal impairment, uncontrolled hypertension, or pre‑existing retinal disease.
Information provided on this page is for educational use by procurement and clinical professionals. Always consult a licensed healthcare provider for medical advice and prescribing decisions. GNH USA supplies this product subject to applicable regulatory and licensing requirements.

Product details

Drug
Binimetinib
Route
Oral Use
Manufacturer
Pierre Fabre Medicament
Origin
EU

Related products