GNH USA

Europe — EMA

Mavenclad

GNH USA supplies Mavenclad (Cladribine), a purine nucleoside analog disease‑modifying therapy for relapsing multiple sclerosis.

Cladribine

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What is Cladribine?

Cladribine, the active ingredient in Mavenclad, is a purine nucleoside analog presented as a 10 mg tablet for oral use. It is indicated for the treatment of relapsing forms of multiple sclerosis in adults, helping to reduce disease activity and slow disability progression.

GNH USA supplies Mavenclad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, with distribution networks across Europe, Asia and the Americas, meeting stringent quality standards for the reliable provision of essential global medicines.

What is Cladribine used for?

Mavenclad is used as a disease‑modifying therapy for multiple sclerosis, targeting the relapsing disease process.

Relapsing‑remitting multiple sclerosis (RRMS): reduces annual relapse rate and slows accumulation of disability. Secondary progressive multiple sclerosis with active disease (SPMS): decreases relapse frequency and mitigates disability progression. Relapsing forms of multiple sclerosis (overall): serves as an immunomodulatory therapy to lower disease activity and delay progression.

What are the side effects of Cladribine?

Cladribine may cause a range of adverse reactions, which are classified by frequency and severity.

Common Side Effects: - Lymphopenia: reduced lymphocyte counts often observed during treatment. - Headache: mild to moderate headache reported by patients. - Nausea: occasional nausea, usually transient. - Fatigue: general tiredness or lack of energy.

Serious or Rare Side Effects: - Severe lymphopenia: profound depletion of lymphocytes increasing infection risk. - Opportunistic infections: including herpes zoster or fungal infections. - Hepatic injury: elevated liver enzymes or hepatitis. - Progressive multifocal leukoencephalopathy (PML): rare but potentially fatal brain infection.

What precautions apply to Cladribine?

When prescribing Cladribine, several precautions and warnings should be observed to ensure patient safety.

Pregnancy: contraindicated; risk of fetal harm classified as Category D. Breastfeeding: not recommended; drug may be excreted in breast milk. Infection risk: monitor for signs of infection and postpone treatment if active infection is present. Blood counts: perform regular monitoring of lymphocyte and complete blood counts during and after therapy. Vaccination: avoid live vaccines during treatment and for several weeks after the last dose. Store at ambient temperature: keep below 25 °C, retain in original packaging, and protect from moisture.

What does Cladribine interact with?

Cladribine can interact with other medicines, affecting its efficacy or safety.

Major Interactions (Avoid): - Live vaccines: concurrent use may cause severe infection; avoid during and after therapy. - Immunosuppressive agents: combined use can markedly increase risk of profound lymphopenia and infection.

Moderate Interactions (Monitor Closely): - Antiviral drugs (e.g., acyclovir): may require dose adjustment due to overlapping immunosuppressive effects. - CYP450 inhibitors: potential to increase Cladribine plasma levels, monitor for toxicity. - Vaccines containing attenuated organisms: schedule appropriately to reduce infection risk.

Frequently asked questions

What is Mavenclad used for?+
Mavenclad is indicated for the treatment of relapsing forms of multiple sclerosis in adult patients. It is used as a disease‑modifying therapy to reduce relapse frequency, slow disability progression, and lower overall disease activity.
How does Cladribine work?+
Cladribine is a purine nucleoside analog that enters lymphocytes and is incorporated into their DNA. This causes DNA strand breaks, leading to apoptosis of activated B and T cells, thereby selectively depleting these immune cells and reducing the autoimmune attack on myelin.
What is the usual dose of Mavenclad?+
The specific dose and treatment schedule of Mavenclad are determined by the prescribing clinician based on the patient’s medical condition, weight, and treatment history. The regimen typically involves oral tablets taken in defined treatment cycles, but exact dosing must be individualized.
Is Mavenclad safe in pregnancy or breastfeeding?+
Mavenclad is classified as pregnancy Category D in the United States and is contraindicated during pregnancy because of potential fetal harm. It is also not recommended for breastfeeding mothers, as the drug may be excreted in breast milk and could affect the infant.
How do I order Mavenclad from GNH USA?+
To order Mavenclad, submit an enquiry on the product page at gnh-usa.com, specifying the required quantity. GNH USA supplies hospitals, pharmacies and procurement teams worldwide, verifies trade or institutional credentials, and then provides pricing, availability, shipping details and any required import documentation.
How does Mavenclad compare with other disease‑modifying therapies for MS?+
Mavenclad offers an oral, short‑course treatment that selectively depletes lymphocytes, whereas many alternatives are injectable or infused and require continuous administration. Its dosing schedule may be more convenient, but the safety profile, especially regarding lymphopenia and infection risk, differs and should be weighed against other options.
How should Mavenclad be stored and handled?+
Mavenclad tablets should be stored at ambient temperature, below 25 °C, in the original packaging to protect them from moisture. Keep the product out of direct sunlight and away from excessive heat or humidity to maintain stability.
How is Mavenclad administered?+
Mavenclad is taken orally as a tablet. The prescribed treatment course usually consists of two treatment weeks per year, separated by several months without medication, but the exact administration schedule is set by the treating physician.
What are the most serious risks associated with Mavenclad?+
The most serious risks include severe lymphopenia leading to opportunistic infections, hepatic injury, and rare cases of progressive multifocal leukoencephalopathy (PML). Patients should be monitored regularly for blood‑cell counts and signs of infection throughout and after treatment.
Who should not use Mavenclad?+
Mavenclad should not be used by individuals who are pregnant, planning to become pregnant, or breastfeeding. It is also contraindicated in patients with active infections, severe hepatic impairment, or a history of malignancy, and in those receiving live vaccines during the treatment period.
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
Cladribine
Route
Oral Use
Manufacturer
Merck Europe B.V.
Origin
EU

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