Wednesday, October 14, 2026
Source trace. Via News points to the documents behind its reporting and shows what we drew from each — so you can check any claim. How we source
Press releaseGlobeNewswire· June 8, 2026

New CNTY-813 Preclinical Data Demonstrate Durable Glucose Control, Immune Evasion Under Alloimmune Pressure, and Scalable Manufacturing at ADA 2026

View original at globenewswire.com
New CNTY-813 Preclinical Data Demonstrate Durable Glucose Control, Immune Evasion Under Alloimmune Pressure, and Scalable Manufacturing at ADA 2026 Advancing CNTY-813 as a potential functional cure in Type 1 DiabetesCNTY-813 iPSC-derived islet replacement therapy demonstrates durable in-vivo glucose control maintained…
Opening lines of the source · GlobeNewswire · short snapshot — read the full document at the original

What we drew from this source

The claims Via News extracted from this document. We point to the source; we don't replace it.

  • T1D affects approximately nine million people worldwide, and while islet cell transplantation has demonstrated potential to restore insulin independence in approximately 70% of patients receiving cadaveric islet transplantation at one year, the current approach requires chronic systemic immunosuppression.

    60% confidence
  • CNTY-813 has the potential to deliver what no prior therapy has achieved: a functional cure for T1D without the need for chronic immunosuppression.

    60% confidence
  • No tumorigenesis was observed in more than 140 mice with more than three months of follow-up across one billion cells infused.

    60% confidence
  • CNTY-813 cells containing Allo-Evasion 5.0 edits provided significant protection from NK cell clearance, induced rapid IgG cleavage of a surrogate anti-drug antibody, and demonstrated protection from antibody-mediated phagocytosis, confirming functional activity across all three engineered immune protection layers.

    60% confidence
  • CNTY-813 has demonstrated critical prerequisites for a potentially curative islet replacement therapy: glucose-responsive function comparable to primary islets, graft stability with no evidence of tumorigenesis, and immune evasion engineered to eliminate the need for chronic immunosuppression.

    60% confidence
  • CNTY-813 iPSC-derived islet cells rapidly restored normoglycemia in streptozotocin-rendered diabetic mice and maintained glucose control for greater than eight months following transplantation.

    60% confidence
  • Allo-Evasion 5.0-edited cells showed comparable glucose control to non-edited cells, confirming immune evasion engineering modifications do not affect the islets' ability to control glucose.

    60% confidence
  • CNTY-813 beta cells comprise greater than 50% of total cell composition, and greater than 98% of cells are in G1 phase, indicating cell cycle exit on par with primary islets.

    60% confidence
  • Mice transplanted with CNTY-813 maintained normal C-peptide secretion function through 42 days post-transplant under allogeneic immune pressure, while unedited islet grafts showed rapid functional deterioration and allo-rejection.

    60% confidence
  • Century Therapeutics is confident in its readiness for clinical trials and the potential to scale for broad patient access, with IND submission on track for Q4 2026 and initial clinical data anticipated in 2H 2027.

    60% confidence

Cited in these Via News reports

What we know · the intelligence behind this page
Live from the substrate
What we're seeing
Q4 2026 Clinical Catalyst Season: Big-Pharma Data Flow, Regulatory Milestones, and a Thin AI-Drug Fringe
October 2026 conferences (EASD, IGCS, NACFC, HFSA) are producing a dense run of late-stage readouts from Novo Nordisk, Lilly, Roche, Bayer, Vertex and Galderma. Regulatory milestones are scheduled behind them: the ivonescimab BLA PDUFA date on 2026-11-14, FDA acceptance of Roche's vamikibart BLA, and Scholar Rock's EMA resubmission. The AI-and-finance angle is peripheral. It consists of the AI-designed drug Rentosertib and QAIAx, a speculative microcap whose trial claims (the QIII pilot, anticipated 2027-01-01, and a patent update) are forecasts and filings rather than data, so they warrant skepticism.
Our read on the data ›
Signals we're tracking
EPKINLY Regulatory-Clinical Success Cascade
High probability of expanded label indications, additional combination approvals, and competitive positioning strength in follicular lymphoma market. Predicts positive commercial uptake and potential accelerated review for related indications.
Patterns we're watching ›
Where sources disagree
ING Group
Both facts record the same metric (shares_outstanding) for ING Group at the identical observation date (2025-12-31). FACT A states 2,902,437,688 shares; FACT B states 2,902 million shares (2,902,000,000). The difference is 437,688 shares (~0.015%). This is a genuine value conflict, though the discrepancy appears to result from FACT B rounding to the nearest million while FACT A provides the precise count.
We flag conflicts openly ›
Recently verified
✓ Checked against the original source
4,986
facts traced to their source — and we flag the ones that don't hold up.
101 entities tracked4,986 facts checked against source5,375 source documents archived
Query this data → isubstrate.com