Product image of Mavenclad (Cladribine) supplied by GNH India

Mavenclad

Active Ingredient:
Cladribine
Origin:
EU

Mavenclad (Cladribine)

Cladribine, the active ingredient in Mavenclad, is a purine nucleoside analog presented as a 10 mg tablet for oral use. It functions as a disease‑modifying therapy that selectively depletes lymphocytes, and is indicated for the treatment of relapsing forms of multiple sclerosis in adult patients.

GNH India supplies Mavenclad as a licensed, GDP‑compliant international pharmaceutical supplier serving hospitals, pharmacies and clinics worldwide, providing reliable access to this multiple‑sclerosis therapy for qualified healthcare providers, ensuring quality and regulatory compliance throughout the supply chain.

Manufacturer / TM Owner

Merck Europe B.V.

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Indications & Clinical Uses

Mavenclad (cladribine) is a disease‑modifying therapy that targets the immune pathway involved in multiple sclerosis.

  • Relapsing‑remitting multiple sclerosis: reduces annualized relapse rate and slows disability progression.
  • Active secondary progressive multiple sclerosis: decreases disease activity and may delay progression.
  • Clinically isolated syndrome with high conversion risk: may lower the likelihood of developing definitive multiple sclerosis.
  • Overall multiple sclerosis disease activity: provides long‑term modulation of immune response to reduce new lesions.

How It Works

  • Cladribine is a purine nucleoside analog that enters lymphocytes and is phosphorylated to its active triphosphate form. The active metabolite incorporates into DNA, causing strand breaks and inhibiting DNA synthesis, which leads to selective depletion of B and T lymphocytes. This reduction of autoreactive lymphocytes diminishes the autoimmune attack on central nervous system myelin, providing a disease‑modifying effect in multiple sclerosis.

Side Effects

Cladribine may be associated with a range of adverse reactions, which are categorized by frequency and severity.

Common Side Effects

  • Lymphopenia: reduced lymphocyte count detected in routine blood work.
  • Headache: mild to moderate head pain reported by some patients.
  • Nausea: occasional feeling of stomach upset or urge to vomit.

Serious or Rare Side Effects

  • Severe or prolonged lymphopenia with opportunistic infections: marked immune suppression leading to infections such as pneumonia or fungal disease.
  • Reactivation of latent viruses (e.g., herpes zoster): shingles‑like eruptions may appear during or after treatment.
  • Progressive multifocal leukoencephalopathy (PML): rare, potentially fatal brain infection linked to JC virus reactivation.

Precautions & Warnings

Before initiating therapy, several safety considerations should be observed.

  • Monitor lymphocyte counts: baseline and periodic testing are required to detect depletion.
  • Assess infection risk: avoid initiating therapy in patients with active infections.
  • Vaccination: administer required live vaccines before treatment; avoid live vaccines during and after therapy.
  • Pregnancy and breastfeeding: contraindicated or not recommended; discuss alternatives with a physician.
  • Renal function: evaluate and adjust use in patients with severe renal impairment.
  • Store at ambient temperature: keep tablets in the original container, protect from moisture and light.

Avoid Interactions

Cladribine can interact with other medicines, necessitating careful review.

Major Interactions (Avoid)

  • Concurrent use of other immunosuppressants: may increase risk of severe infection.
  • Live vaccines: contraindicated during treatment and for several months after the last dose.
  • Antiviral agents that rely on lymphocyte function: potential additive immunosuppression.

Moderate Interactions (Monitor Closely)

  • CYP450 substrates: cladribine is not a strong inhibitor but monitor plasma levels of sensitive drugs.
  • Non‑live vaccines: may have reduced efficacy; assess immune response.
  • Hormonal contraceptives: no known interaction, but standard monitoring is advised.

Frequently Asked Questions

Mavenclad is prescribed as a disease‑modifying therapy for adults with relapsing forms of multiple sclerosis. It helps reduce the frequency of clinical relapses and may slow the accumulation of disability by targeting the immune system that drives disease activity.

Cladribine is a purine nucleoside analog that is taken up by lymphocytes and phosphorylated to an active form that incorporates into DNA. This interferes with DNA synthesis, leading to selective depletion of B and T cells, thereby reducing the autoimmune response responsible for multiple sclerosis lesions.

The exact dose and treatment schedule for Mavenclad are determined by the prescribing physician based on the patient’s clinical profile and regulatory guidelines. Dosing is individualized and should follow the prescriber’s instructions; patients should not adjust the dose on their own.

The safety of Mavenclad in pregnancy and lactation has not been established. It is generally advised to avoid use in pregnant or nursing women unless the potential benefit justifies the potential risk. Women of child‑bearing potential should use effective contraception during treatment and for a defined period afterward.

To request Mavenclad, 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.

Mavenclad is an oral, short‑course disease‑modifying therapy that selectively depletes lymphocytes, whereas many alternatives are injectable or continuous oral agents. Its intermittent dosing schedule can be convenient, but it requires careful monitoring of immune cells. The choice depends on efficacy, safety profile, patient preference and physician assessment.

Mavenclad tablets should be stored at ambient temperature, below 25 °C. Keep them in the original blister pack, protect from moisture and light, and store out of reach of children. Do not refrigerate or freeze the tablets.

Mavenclad is taken orally as a tablet. The prescribed treatment course typically involves taking the tablets on specific days within two treatment weeks, separated by a year‑long interval, but the exact administration schedule must be followed as directed by the treating physician.

The most serious risks include severe or prolonged lymphopenia that can lead to opportunistic infections, reactivation of latent viruses such as herpes zoster, and the rare occurrence of progressive multifocal leukoencephalopathy (PML). Patients should report any signs of infection or unusual neurological symptoms promptly.

Mavenclad should be avoided in individuals with active infections, severe renal impairment, known hypersensitivity to cladribine, or those who are pregnant or breastfeeding without a clear medical justification. It is also contraindicated in patients receiving other potent immunosuppressive therapies unless specifically approved by a specialist.

Published by

GNH India Pharmaceuticals Limited

Licensed pharmaceutical supplier

Last updated:

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