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Manufacturer / Innovator:
Germany
Regulatory Approval:
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Mavenclad (cladribine) is a purine antimetabolite that reduces the immune cells involved in multiple sclerosis relapses. It is indicated for the treatment of:
Due to its safety profile, Mavenclad is generally recommended for patients who have had an inadequate response to, or are unable to tolerate, other MS therapies. It is a prescription medicine and must be used under the supervision of a qualified neurologist.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
Boxed Warning — Mavenclad: Mavenclad may increase the risk of malignancy and is contraindicated in patients with a current malignancy. It also carries a risk of teratogenicity and is contraindicated in pregnant women and in patients of reproductive potential who do not plan to use effective contraception.
Step 1 – Search & request your medicine: The patient or treating doctor submits a request with basic details to initiate the access process.
Step 2 – Verification & eligibility review: The team verifies availability and reviews eligibility against regulatory and clinical requirements to ensure a compliant pathway.
Step 3 – Receive quote & delivery timeline: A transparent quotation is shared, covering medicine cost, logistics, and a clear delivery timeline.
Step 4 – Regulatory approval process: Assistance is provided to secure the approvals and documentation required for legal cross-border access.
Step 5 – Temperature-controlled import & handling: The medicine is sourced and transported under strict GDP-compliant conditions to maintain product integrity.
Step 6 – Secure delivery: The medicine is delivered to the patient or treating hospital, with updates provided at each stage.
Note: From request to delivery, every step is designed to ensure your treatment reaches you safely, compliantly, and without unnecessary delays.
Mavenclad (cladribine) tablets may be imported in the patient's name only, by patients or government hospitals, in line with India's import regulations for unapproved medicines. The following documentation is required:
The order is confirmed only after receipt and verification of a valid prescription from the doctor and, if applicable, an import permit.
Mavenclad (cladribine tablets) is a prescription medicine that legally requires a doctor's prescription to be dispensed. As of current publicly available information, Mavenclad is not commercially marketed in India.
However, patients in India can legally access Mavenclad through the Named Patient Program (NPP) — an import provision that allows patients to receive medicines approved in other countries but not yet marketed in India, under a doctor's prescription and proper regulatory documentation.
Mavenclad received US FDA approval in March 2019 for relapsing forms of multiple sclerosis, ensuring full transparency throughout the process.
Mavenclad can be made available to patients, doctors, and hospitals across major cities in India, including Gurgaon, Delhi, Bangalore, Mumbai, Navi Mumbai, Thane, Hyderabad, Mysore, Kerala, Chennai, Coimbatore, Madurai, Kolkata, Ahmedabad, Surat, Vadodara, Pune, Nagpur, Nashik, Jaipur, Udaipur, Lucknow, Kanpur, Gorakhpur, Chandigarh, Mohali, Faridabad, Noida, Ghaziabad, Kochi, Trivandrum, Kozhikode, Thrissur, Kannur, Mangalore, Bhubaneswar, Patna, Ranchi, Raipur, Guwahati, Visakhapatnam, Vijayawada, Goa, Jammu, Srinagar, Dehradun, Bhopal, Indore, Ludhiana, Amritsar, and others.
Mavenclad is sourced directly from authorized channels in the country of origin and shipped to India under GDP-compliant logistics to preserve product integrity from dispatch to delivery.
Named Patient Program supports access to Mavenclad for patients with relapsing forms of multiple sclerosis across major cities in India, coordinating documentation, sourcing, and delivery with treating neurologists.
Patients in Mumbai can access Mavenclad through NPP with support from treating neurologists at the city's leading MS care centers.
In Delhi, NPP coordinates with hospitals and specialty neurology clinics to facilitate timely access to Mavenclad.
Bangalore's neurology centers work with NPP to support patients requiring Mavenclad.
Patients in Chennai can access Mavenclad through NPP, with coordination between treating doctors and the program's regulatory and logistics team.
Hyderabad's neurology centers support diagnosis and access coordination for Mavenclad through NPP.
NPP facilitates access to Mavenclad for patients in Kolkata under the guidance of treating neurologists.
Patients in Pune can access Mavenclad through NPP with prescription-based coordination and delivery support.
NPP supports access to Mavenclad for patients in Ahmedabad, working directly with treating specialists.
Patients in Kochi and across Kerala can access Mavenclad through NPP's regulated import pathway.
NPP coordinates access to Mavenclad for patients in Chandigarh and the surrounding region.
Patients in Jaipur can access Mavenclad through NPP with support from treating neurologists.
NPP facilitates access to Mavenclad for patients in Lucknow and across Uttar Pradesh.
Patients in Bhubaneswar can access Mavenclad through NPP's coordinated import and delivery process.
NPP supports access to Mavenclad for patients in Guwahati and across the Northeast region.
NPP also supports access for patients in other Indian cities not listed above — contact the team to check availability and timelines for your location.
Written By: Nitin Goswami, Senior Medical Content Writer
Last Updated: 09 September 2026
Sources: FDA • CDSCO
Medically Reviewed By: Shilpi Banerjee, Registered Pharmacist (M.Pharm)
Last Updated: 09 September 2026
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