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Supplied with complete CDSCO-approved import and customs documentation, including Form 12A & 12B, CDEC, GST Bill of Entry, Commercial Invoice, and Packing List.
Manufacturer / Innovator:
Germany
Regulatory Approval:
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Temperature-controlled logistics ensuring safe, reliable, and timely medicine delivery.
Cablivi (caplacizumab-yhdp) is a von Willebrand factor-directed antibody fragment. It is indicated, in combination with plasma exchange and immunosuppressive therapy, for the treatment of:
It is a prescription biologic used in a hospital setting alongside plasma exchange therapy, and must be administered under the supervision of a qualified hematologist.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
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, cold-chain 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.
Cablivi (caplacizumab-yhdp) injection 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. Given the urgent nature of aTTP treatment, expedited coordination is prioritized.
Cablivi (caplacizumab-yhdp injection) is a prescription medicine that legally requires a doctor's prescription to be dispensed. As of current publicly available information, Cablivi is not commercially marketed in India.
However, patients in India can legally access Cablivi through the Named Patient Program (NPP) — an import provision that allows a medicine not yet registered in India to be imported in the name of a specific patient for their personal treatment, under a valid prescription.
Cablivi has been FDA approved since 2019, ensuring full transparency throughout the process.
Cablivi 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 — and can facilitate delivery to the patient's treating hospital. Orders are confirmed only after receipt of a valid doctor's prescription and an import permit, where applicable.
NamedPatientProgram.com (NPP) can source Cablivi from reliable global channels and facilitate supply to patients, doctors, and hospitals under applicable legal provisions. As a temperature-sensitive biologic, Cablivi requires cold-chain handling throughout transit and must be kept refrigerated between 2°C to 8°C, protected from light. All prescriptions are dispensed and checked by registered pharmacists and dispatched from New Delhi, India, after legal requirements are fulfilled.
For Cablivi cost in India and availability, contact NPP via WhatsApp at +91 98104 69557 | Toll-Free: 1800-1200-365 or email info@namedpatientprogram.com.
Patients across India can access Cablivi through regulated import pathways, with delivery arranged to the treating hospital based on a valid hematologist's prescription, alongside plasma exchange therapy.
A major hematology hub with institutions like Tata Memorial, Mumbai coordinates access to aTTP therapies like Cablivi for eligible patients.
As part of the Delhi NCR region, the city has a strong concentration of hematology specialists, making it a key location for accessing aTTP treatments.
With a growing network of multispecialty hospitals, Bangalore supports access to Cablivi through structured import pathways guided by treating specialists.
Home to several reputed hematology centers, Chennai facilitates access to Cablivi for patients with acquired thrombotic thrombocytopenic purpura.
A growing hub for specialty care, Hyderabad supports coordinated access to Cablivi for eligible patients under specialist supervision.
Eastern India's leading medical centers in Kolkata coordinate Cablivi access for patients with aTTP.
With an expanding base of hematology clinics, Pune facilitates timely access to Cablivi under prescription.
Gujarat's leading hospitals support regulated access to Cablivi for eligible patients.
Kerala's healthcare network, including major hospitals in Kochi, coordinates access to advanced biologics like Cablivi.
Serving North India, Chandigarh's specialist centers facilitate access to Cablivi for patients from Punjab, Haryana, and Himachal Pradesh.
Rajasthan's leading hospitals support patient access to Cablivi through the Named Patient Program.
A key referral center for North India, Lucknow facilitates coordinated access to Cablivi under specialist care.
Odisha's growing specialty healthcare sector supports patient access to Cablivi.
As a referral hub for the North-East, Guwahati facilitates access to Cablivi for patients across the region.
Access can also be coordinated for patients in other major Indian cities, subject to a valid prescription and regulatory requirements.
Written By: Nitin Goswami, Senior Medical Content Writer
Last Updated: 08 September 2026
Sources: FDA • CDSCO
Medically Reviewed By: Shilpi Banerjee, Registered Pharmacist (M.Pharm)
Last Updated: 08 September 2026
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