November 06, 2025

NexCAR19 cancer drug made gene therapies affordable, accessible with patient safety: Govt

NexCAR19, India's first humanised CAR-T therapy, makes gene treatments affordable for cancer patients while maintaining scientific quality and patient safety standards.

India's Cancer Breakthrough: How NexCAR19 Makes Gene Therapy Affordable

World's first humanised CAR-T therapy developed entirely in India

Treats relapsed B-cell lymphomas and acute lymphoblastic leukemia

Developed by ImmunoACT with IIT Bombay and DBT support

New GMP facility to treat 1000+ patients annually

NexCAR19, the world's first humanised CAR-T therapy developed in India, has made gene therapies affordable and accessible while also maintaining scientific quality and patient safety, said the Ministry of Science and Technology on Wednesday.

"NexCAR19, India's first living drug, has made gene therapies both affordable and accessible without compromising scientific rigour or patient safety - Ministry of Science and Technology"

NexCAR19 is a prescription drug for treating specific relapsed or refractory B-cell Non-Hodgkin's Lymphomas and B-cell Acute Lymphoblastic Leukaemia when frontline therapy or other standard treatments have been unsuccessful. It was developed using a lentiviral vector.

"NexCAR19, India's first living drug, has made gene therapies both affordable and accessible without compromising scientific rigour or patient safety," the Ministry said.

NexCAR19, developed by ImmunoACT -- a gene therapy company incubated at IIT Bombay -- and supported by the Department of Biotechnology (DBT) and Biotechnology Industry Research Assistance Council (BIRAC), was among the three path-breaking innovations gifted to the nation by Prime Minister Narendra Modi at the ongoing ESTIC2025 conclave in the national capital.

The other two include QSIP: India's own quantum security chip; and 25-qubit QPU: India's first quantum computing chip, powering the future of computation.

CAR-T, or the Chimeric Antigen Receptor T-cell, has emerged as a breakthrough in cancer treatment. Clinical trials conducted globally have shown promising results in end-stage patients, especially in patients suffering from Acute Lymphocytic Leukaemia.

Recently, DBT via the Biomanufacturing initiative under the BioE3 Policy gave funding to ImmunoAct for setting up a 200L GMP lentiviral vector and plasmid platforms to scale up the production and also to make this new therapeutic modality more affordable.

"This platform will likely incorporate advanced bioreactor technologies to facilitate high-density cell growth and continuous production and enable higher yields and better performance of lentiviral vectors. The GMP-grade gene delivery vector can help at least 1000 patients per year for cell and gene therapy," the Ministry said.

Amid rising cancer cases in the country, the DBT is also promoting early and late translational research to develop novel and indigenous CAR-T-based therapeutics to combat the deadly disease.

DBT is supporting interdisciplinary teams to venture into immunotherapeutic solutions for a broader spectrum of cancers, including both liquid and solid cancers, and also ways to overcome the associated toxicities, the Ministry added.

This includes cancers like Multiple Myeloma (MM), Acute Lymphocytic Leukemia, refractory or relapsed B-cell Acute Lymphoblastic Leukemia, glioblastoma, etc.

India's First CAR-T Therapy NexCAR19 Launched by Modi

India has achieved a major medical breakthrough with the development of NexCAR19, the country's first humanised CAR-T therapy. This innovative treatment makes gene therapies affordable and accessible for cancer patients without compromising on safety standards. Developed by ImmunoACT with support from IIT Bombay and government agencies, it specifically targets relapsed B-cell cancers. The therapy was officially launched by Prime Minister Modi at the ESTIC2025 conclave alongside other technological innovations.

https://www.newkerala.com/news/o/nexcar19-cancer-drug-made-gene-therapies-affordable-accessible-patient-488

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