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 iPSC
PLATFORM
Allo-Evasion™ Targets Indications Clinical Trial Research Ind-enabling Clinical P1 P2 P3
Autoimmune Diseases
CNTY-101
iNK
1.0
CD19
B-cell-mediated autoimmune diseases
CARAMEL IST1
CARAMEL IST1
CNTY-308
αβ ιΤ
5.0
CD19
B-cell-mediated autoimmune diseases​
CNTY-813
Beta Islet cells
5.0
Beta Islet Transplantation
Type 1 Diabetes
CNTY-341
αβ ιΤ
5.0
CD19 + CD22
B-cell malignancies
Solid Tumors
Solid tumors
iT
5.0
Nectin-4/other
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-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.

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-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.