Affordability
One batch — many patients
Allogeneic donor-derived therapies reduce manufacturing cost by enabling multi-patient batches.
TiCoBi
Thrafford is developing India’s first scalable, off-the-shelf γδ T-cell therapy manufacturing platform, designed to eliminate measurable residual disease (MRD) before it causes AML relapse.
The platform
A proprietary, patent-filed, time-controlled bioprocess that expands a single healthy donor’s blood into up to 15 ready-to-use, off-the-shelf γδ T-cell doses — with no viral vectors, no gene editing and no patient-specific manufacturing.
Blood from a single healthy donor — not the patient.
Gamma-delta T cells are isolated and purified ex vivo.
Temporally and volumetrically controlled expansion yields a non-exhausted memory phenotype.
Off-the-shelf doses, ready when the clinician needs them.
Immune cells that find leukaemia without a map
Immune-mediated elimination of leukaemia is most likely to work when disease burden is minimal — before overt relapse and an increasingly immunosuppressive microenvironment.
γδ T cells recognise stress-induced ligands (MICA/B and ULBP family) on residual leukaemic cells, independently of classical HLA presentation.
Potent anti-leukaemic activity with minimal risk of graft-versus-host disease — the basis for allogeneic, off-the-shelf therapy.
Suited to repeated administration during remission or in the peri-transplant setting, when disease burden is lowest.
Applications
Our reagent-agnostic design reaches across oncology and autoimmune disease. Longer term, our AI and quantum computation initiative designs and optimises targets, algorithms and processes.
Product portfolio
TiCoBi is antigen-agnostic. Beyond AML, the same process extends to glioblastoma and other solid tumours — and TiCoBi-generated γδ T cells can also supply partners’ CAR-T programmes.
In low- and middle-income countries, including India, accessibility remains a major challenge, which is why adopting PoCMAP can be a revolutionary intervention.
Point-of-care with PoCMAP
In conventional manufacturing, a patient’s cells are collected at the hospital, frozen and shipped to a distant facility, then frozen again and shipped back for infusion. Decentralising manufacturing to the hospital removes both journeys, reducing logistics and freeze–thaw cycles.
5Cell to patient without leaving the building: no inter-site shipping and fewer freeze–thaw cycles.
Therapies are produced at the hospital, where the patient is treated.
Multiple batches run side by side to increase output.
Works with CAR-T, NK and dendritic cell systems.
Real-time sterility and quality control integration.
Reduced logistics and fewer freeze–thaw cycles.
Platform principles
Affordable. Scalable. Accessible.
One batch — many patients
Allogeneic donor-derived therapies reduce manufacturing cost by enabling multi-patient batches.
40× production capacity
Our modular platform delivers up to 40× capacity using parallel multi-batch processing systems.
Therapies closer to home
India’s first point-of-care CAR-T manufacturing system — enabling hospital-based therapy production.
Intellectual property
Our moat combines patent-filed manufacturing with trade-secret process logic — an integrated value chain that takes years of validation to rebuild.
Application no.
2026••••2935
Application no.
2025••••8309
Application no.
2025••••2865
Ongoing project
We are mapping how human genes, proteins, metabolites, drugs and cells interact, drawing on the largest possible census of biomedical data resources and structuring it for quantum AI. The first goal is a working simulation of the immune system; every layer we add opens new questions, from cancer to autoimmunity and ageing.
Conventional AI
Quantum AI
Simulating how a patient’s immune system may respond to a cell therapy, including cytokine release syndrome and neurotoxicity, before the first dose.
Ranking the stress ligands, receptors and pathways worth pursuing in future γδ T-cell and CAR-T programmes.
Identifying the patients most likely to respond, from the molecular profile of their disease.
Finding approved drugs that act on the same interaction networks as a disease, as candidates for new uses.
Talk to us about clinical partnerships, our γδ T-cell programmes, or supplying γδ T cells for your CAR-T pipeline.