Impact of NexCAR 19

90%

Remission Rate

200+

Patients Treated

2x

Likely To Stay Cancer-free

2yrs

Longest Remission Rate

CAR-T Cell Therapy

Harnessing Your Immune System to Fight Cancer Safely

India faces a growing cancer burden, ranking second globally in cancer mortality. For aggressive B-cell malignancies like Acute Lymphoblastic Leukemia (blood cancer) and Large B-cell Lymphoma (lymph node cancer), over 40% of patients relapse or resist chemotherapy and other standard treatments.

ImmunoACT brings revolutionary CAR-T cell therapy for cancer treatment in India, where a patient’s own immune cells are genetically modified to recognize and destroy cancer cells. This groundbreaking approach has demonstrated remarkable improvements in overall survival and offers new hope for patients seeking advanced CAR-T therapy in India with limited treatment options.

Real Stories of Hope

At ImmunoACT, we believe that every patient story matters. Our CAR-T cell therapies are transforming lives-bringing hope where options were once limited. These powerful testimonials reflect not only the resilience of our patients but also the impact of cutting-edge, gene-modified cell therapy. As we work alongside leading healthcare institutions, academic collaborators, and strategic partners, our mission remains clear: to expand equitable access to advanced immunotherapies and redefine cancer care in India and beyond.

Our Manufacturing Facility

At ImmunoACT, our advanced manufacturing facility is purpose-built to deliver high-quality, safe, and scalable cell and gene therapies. With the capacity to treat up to 750 patients annually, we ensure timely and consistent access to life-saving treatments.

Built for Precision. Designed for Patients.

WHO-Certified GMP Facility
Compliant with global quality and safety standards ensuring purity, consistency, and efficacy in every therapy.
98% Manufacturing Success Rate
Industry-leading cell engineering success across all patient cohorts, minimising failures and therapy delays.
↑ 98% Success Rate
Scalable Treatment Capacity
Expanding from 750 to 1,500 patients per year to meet growing demand and reduce wait times.
↑ 1,500 Patients / Year
End-to-End Manufacturing
Fully integrated — from plasmid design to viral vector production and ex-vivo cell engineering.
Rapid & Reliable Delivery
Streamlined operations for fast turnaround, ensuring therapies reach patients when they need them most.
Global-Standard Quality Control
Dedicated QC/QA units rigorously test and validate each batch before release.
Clinician-Centric Support
Backed by experts in clinical trials, regulatory affairs, and treatment logistics to simplify doctor workflows.
Patient-Focused Outcomes
Designed with one goal: enabling safe, accessible, and effective therapies for every patient.
Traceability & Audit Integrity
Full chain-of-identity tracking from apheresis to infusion-ready product, meeting global compliance standards.

Partnered Hospitals

Our strong association with over 80 leading cancer treatment hospitals in India ensures hassle-free treatment with our CAR-T cell therapies.

Find A Treatment Centre Near You

Strategic Collaborations

To advance the research and development of our innovative gene-modified cell therapies, we are fostering relationships across academia, healthcare institutions, and strategic partnerships with the intent to equitize access.

Stories of Hope

Ramnath Vishnu

Cancer Survivor

After years of setbacks with traditional treatments, CAR-T cell therapy changed everything. The idea of using my own cells to fight the cancer gave me hope. Now, I’m in remission, and I feel like I’ve truly gotten my life back. I can finally look forward to the future without fear.

Ramnath Vishnu

Cancer Survivor

After years of setbacks with traditional treatments, CAR-T cell therapy changed everything. The idea of using my own cells to fight the cancer gave me hope. Now, I’m in remission, and I feel like I’ve truly gotten my life back. I can finally look forward to the future without fear.

Ramnath Vishnu

Cancer Survivor

After years of setbacks with traditional treatments, CAR-T cell therapy changed everything. The idea of using my own cells to fight the cancer gave me hope. Now, I’m in remission, and I feel like I’ve truly gotten my life back. I can finally look forward to the future without fear.

Stories of Hope

Ramnath Vishnu

Ramnath Vishnu

Cancer Survivor

After years of setbacks with traditional treatments, CAR-T cell therapy changed everything. The idea of using my own cells to fight the cancer gave me hope. Now, I'm in remission, and I feel like I've truly gotten my life back. I can finally look forward to the future without fear.
Sarah Mitchell

Sarah Mitchell

Cancer Survivor

The personalized approach of CAR-T therapy made all the difference. When conventional treatments weren't working, this innovative treatment gave me a second chance at life. Today, I'm cancer-free and grateful for every moment.
David Kumar

David Kumar

Cancer Survivor

I had almost given up hope until I learned about CAR-T cell therapy. The journey wasn't easy, but the results were worth it. Now I'm back to living life to the fullest, surrounded by my loved ones.

Real Stories of Hope

Ramnath Vishnu

Cancer Survivor

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Ramnath Vishnu

Cancer Survivor

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Ramnath Vishnu

Cancer Survivor

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Frequently Asked Questions

What is Leukapheresis and how does NexCAR19 involve it?
This is the process by which a patient's immune-effector cells are extracted through a machine. A bag of these extracted cells is transported under refrigerated conditions to ImmunoACT. From these, At our facility, we select and activate T-cells on which we manufacture NexCAR19. To be delivered for infusion to the patient.
Why does it take a few weeks for NexCAR19 to be administered?
NexCAR19 is made from a patient's own T-cells. The cells are sent to our controlled laboratory, cultured, modified, and then multiplied to reach a desirable dose. This takes ~19 days from Leukapheresis.
How many days after the therapy would CRS be expected?
Cytokine Release Syndrome (CRS) is the most frequent after-effect of the therapy, but it is expected within the first 4 weeks of the infusion, not long term.
How common are the serious side effects?
In our clinical trials, severe symptoms were seen in ~5% of patients. These side effects may depend upon several factors, including the pre-existing disease burden and your clinical condition.
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