Pipeline

Pipeline Overview

We have assembled a robust portfolio of allogeneic, iPSC-derived cell therapies in autoimmune disease and cancer. All of our product candidates incorporate our proprietary Allo-Evasion™ technology to avoid host rejection and potentially increase the durability of clinical responses.
Product Targets Indications Clinical Trial Research IND-enabling Clinical Phase 1 Phase 2 Phase 3
Autoimmune Diseases
Priority Program
CNTY-813 Beta Islet cells (Allo-EvasionTM 5.0)
Beta Islet Transplantation
Type 1 Diabetes
Additional Programs
CNTY-308 αβ ιΤ (Allo-EvasionTM 5.0)
CD19
B-cell-mediated autoimmune diseases​
CNTY-101 iNK (Allo-EvasionTM 1.0)
CD19
B-cell-mediated autoimmune diseases
CARAMEL IST1
CARAMEL IST1
Multiple iT (Allo-EvasionTM 5.0)
Multiple
B-cell-mediated autoimmune diseases, solid tumors, others
Solid Tumors
Undisclosed

Hematologic tumors​

Solid Tumors

Autoimmune Diseases

1Agreement in place for an investigator sponsored trial (IST) by Professors Georg Schett and Andreas Mackensen at Friedrich-Alexander University Erlangen-Nürnberg.

CNTY-813

CNTY-813 is comprised of iPSC-derived beta islets engineered with Allo-Evasion™ 5.0 and designed to protect from T cell, NK cell and humoral immune rejection, with the goal of durable glycemic control without the need for systemic immunosuppression. CNTY-813 is being developed as a potential treatment for type 1 diabetes.

CNTY-308

CNTY-308 is a CD19-targeted CD4+/CD8+ ab CAR-iT cell therapy functionally comparable to primary T cells and engineered with Allo-Evasion™ 5.0. CNTY-308 is being developed as a potential treatment for B-cell-mediated diseases.

CNTY-101

CNTY-101 is a CAR-iNK cell therapy with six precision gene edits as a potential treatment for patients with B-cell-mediated autoimmune diseases.