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Ready to proceed? Start a request for Adebrelimab on our secure patient portal to submit your prescription, upload documents and track your approval status.
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:
China
Regulatory Approval:
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Adebrelimab is a cancer immunotherapy made in China by Jiangsu Hengrui Pharmaceuticals, where it is sold as 艾瑞利® (Arelili). It is used for small cell lung cancer that has already spread beyond one area of the chest, known as extensive-stage disease. Rather than killing cancer cells itself, it helps the patient's own immune system find the tumour and fight it.
It is approved by China's National Medical Products Administration (NMPA) for adults with:
It is a prescription cancer medicine and should only be used under an oncologist experienced in cancer treatment. If you want to understand the disease itself first, our guide to small cell lung cancer explains it in plain language.
Many tumours hide behind a protein called PD-L1, which tells the immune system's T cells to stand down. This medicine is a humanised IgG4 antibody that latches on to PD-L1 and blocks that signal, so the T cells can go back to attacking the cancer.
The approval is based on CAPSTONE-1, a study of 462 people with untreated ES-SCLC published in The Lancet Oncology in 2022. With chemotherapy plus adebrelimab, median survival was 15.3 months, against 12.8 months with chemotherapy alone. The gap widened with time: at two years, 31.3% of patients on the combination were alive, compared with 17.2%.
The dose is not raised or lowered for side effects; instead, the doctor pauses or stops treatment. To give a sense of quantity, someone weighing 60 kg needs 1,200 mg per dose, which is two vials.
This information is not a treatment plan. For personalized medical advice, consult your doctor and refer to the full prescribing information.
Immune-related side effects: by switching the immune system back on, this kind of medicine can also turn it against healthy organs. Such reactions may start during treatment or months after the last dose, and a small number in the trials were serious or fatal. Most improve once treatment is paused and steroids are given, which is why early reporting matters.
Common side effects: alongside chemotherapy, the most frequent were hair loss (44.3%), nausea (40.0%), loss of appetite (29.6%), vomiting (26.1%), tiredness (18.3%), constipation (17.4%) and an underactive thyroid (12.2%). Low blood counts were very common, as they are with the chemotherapy itself. Only 1.7% of patients had to stop the antibody for good because of side effects.
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.
The injection can be imported only in the patient's name, by the patient or a government hospital, in line with India's import regulations for unapproved medicines. You will need:
Once we have received and checked a valid prescription and, where needed, an import permit.
Not over the counter. It is approved only in China. It has no CDSCO approval and is not sold in Indian pharmacies, and the US FDA and European Medicines Agency have not approved it either.
Patients can still get it legally through the Named Patient Program (NPP). Under this route, a medicine that is not registered in India is imported for one specific patient, on that patient's prescription.
It 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) sources this medicine through the manufacturer's authorised supply channels in China and arranges supply to patients, doctors, and hospitals under applicable legal provisions. The vials must stay between 2°C and 8°C, away from light, and must never freeze, so they travel under temperature-controlled shipping from pickup to hospital. All prescriptions are dispensed and checked by registered pharmacists and dispatched from New Delhi, India, after legal requirements are fulfilled.
For the current 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 this medicine through regulated import pathways, with delivery arranged to the treating hospital on a valid oncologist's prescription.
One of the country's busiest centres for lung cancer care. Vials are delivered straight to the treating hospital's pharmacy against the named-patient papers.
Cancer hospitals here receive patients from across North India. Being close to our New Delhi dispatch point keeps the cold-chain journey short.
Oncologists at the city's multispecialty and cancer hospitals can request the medicine for a specific patient, with the quote shared before anything is ordered.
A long-standing referral hub for South India, used to handling refrigerated imported biologics.
Delivery is planned around the patient's 3-weekly infusion date, so the vials arrive on time for each cycle.
For Kolkata and the eastern states, shipments are routed so the vials stay within 2°C to 8°C all the way.
Patients here can use the same documented import route, with updates at each stage of the shipment.
The treating oncologist can share the prescription and reports with us to start the import in the patient's name.
Patients across Kerala can have the medicine delivered to their hospital in Kochi or nearby cities.
Serves patients from Punjab, Haryana and Himachal Pradesh, with delivery to the hospital where treatment is given.
Patients in Rajasthan can start treatment without travelling abroad, as long as the import is in their name.
We coordinate delivery to both public and private cancer hospitals in Lucknow and across Uttar Pradesh.
Odisha's growing cancer care centres can receive the medicine for named patients.
As the referral hub for the North-East, Guwahati hospitals can receive cold-chain deliveries for patients from the whole region.
Access can also be coordinated for patients in other Indian cities, subject to a valid prescription and regulatory requirements.
Written By
Nitin GoswamiDeputy Manager – Content & Social Media, Ikris Pharma Network
Sources: NMPA • CDSCO
Last Updated: 16 October 2026
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