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The iPSC platform

From a tube of blood
to an injectable therapy.

The first fully characterized, HLA-matched allogeneic iPSC cell bank in the world. Built from 85,000 consented donors. Manufactured in Boston.

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Why HLA
matching matters
Immune compatibility.
The same immune-compatibility system used in organ transplantation for the past four decades, applied to cell therapy.

Human leukocyte antigen, or HLA, is the molecular signature the immune system uses to tell its own tissue from someone else's. Transplant medicine has spent four decades learning how to match donors and recipients on these signatures so that the transplanted organ is not rejected.

We apply the same principle to cell therapy. The donors we use are HLA-homozygous, which means they carry two identical copies of each marker at the loci that matter. That homozygosity makes a single donor compatible with a far larger fraction of the population than an ordinary donor would be. Sixty-five such donors, chosen carefully, cover more than nine of every ten Americans.

What our cells do

Carry an immune signature the patient's body recognizes as compatible.
A single matched donor line can be transplanted into millions of recipients without rejection.
Eliminate the need for immunosuppressive drugs.
The patient receives the therapy and goes home. No daily immune-suppressing regimen.
Open chronic indications that current cell therapies cannot reach.
Knee osteoarthritis, cardiac disease, and other long-term conditions become viable targets.
Preserve natural HLA presentation, no gene editing required.
The immune system recognizes the cells as self, rather than as a hidden or unverifiable entity.
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From blood
to therapy
The process.
From the moment a donor's blood is drawn to the moment a matched vial is thawed for a patient, every line passes through the same controlled path. A decade of refinement sits behind each stage.
Step 01
Collect
A consented HLA-typed super donor gives a single tube of blood.
Step 02
Reprogram
Peripheral blood cells are reprogrammed into iPSCs using a Sendai virus that does not integrate into the genome.
Step 03
Characterize
Pluripotency, safety, and karyotype are confirmed on every line before it enters the bank.
Step 04
Differentiate
The iPSCs are turned into the target cell type using xeno-free protocols.
Step 05
Bank
Vials are cryopreserved at minus 195 degrees Celsius in liquid nitrogen.
Step 06
Match and inject
The patient is HLA-typed, a matching donor line is selected, a vial is thawed, and the cells are delivered.
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One bank,
many cell types
Differentiation pathways.
Every cell line in the bank can be differentiated into multiple lineages. The same donor source supplies the inputs for several therapeutic programs at once.
Chondrocytes
Cartilage repair, the active cell type behind G3N-004.
Stage: IND-track
Cardiomyocytes
Cardiac therapy and disease modeling, the basis of G3N-008.
Stage: Preclinical
Mesenchymal stem cells
Immune modulation and tissue repair across multiple indications.
Stage: Established
Neurons
Neurodegeneration models and therapy candidates, the foundation of G3N-012.
Stage: In development
Hepatocytes
Liver disease modeling and predictive toxicology.
Stage: Established
T cells
Allogeneic CAR-T for oncology, currently at the patent stage.
Stage: Patent stage
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Every line,
fully characterized
Characterization.
Every iPSC line in the bank carries a full characterization dossier. Identity, stability, pluripotency, and safety are documented on each vial. The bank is a clinical-grade inventory, not a research collection.
Pluripotency
Flow cytometry confirms expression of SOX2, TRA-1-60, and SSEA4. The cells retain the developmental flexibility required to become any therapeutic cell type the platform supports.
Genetic stability
G-banding karyotype and SNP array analysis confirm that the genome remains intact across the reprogramming process. The line is a faithful copy of the donor it came from.
Safety
Sendai virus clearance, mycoplasma testing, and sterility verification are run on every vial. Each result is recorded in the certificate of analysis.
Identity
STR profiling and high-resolution HLA confirmation establish a documented chain of identity from donor through reprogramming through every banked vial.
[ Talk to us about the platform ]

Researchers, drug discovery teams,
partners.

If you are working on AI drug discovery, allogeneic cell therapy, or non-animal models and you want to understand what the bank can do for your program, the door is open.