REDEFINING THE FUTURE OF CAR T

Allogene is working to overcome the limitations of autologous CAR T therapies by creating investigational allogeneic CAR T cell products, or AlloCAR T™ products. Unlike autologous cell therapy, AlloCAR T™ products use T cells from healthy donors.

These cells are isolated in a manufacturing facility, engineered to express CARs to recognize and destroy disease, and modified via gene editing to limit autoimmune response when given to a patient. These products are then stored for "off-the-shelf" use on demand. We believe that, at scale, a single manufacturing run has the potential to yield treatment for 100+ patients.

Doing What No Autologous Treatment Has Done Before

Assess

ACCESS

  • Potential to treat all eligible patients
  • No need for complex logistics
Cost

COST

  • Scalable and efficient manufacturing
  • Potential to treat 100+ patients from a single manufacturing run
  • Lower ancillary costs
Reliability

SPEED/RELIABILITY

  • "Off-the-shelf" for on-demand treatment
  • Less product variability, made from healthy T cells
Innovation

INNOVATION

  • Multiplex
    gene-engineering and gene-editing capabilities
  • Opportunity for product optimization

The next revolution in cell therapy is the development of AlloCAR T™ products engineered from the T cells of healthy donors. These "off-the-shelf" CAR T products, enhanced by gene editing, could be the next most important breakthrough in the field.

THE DIFFERENCE STARTS WITH HEALTHY DONORS

CarT Donor Cells
Healthy Donor
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CAR T Cells
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100 Patients

AlloCAR T™ PRODUCTS HAVE THE POTENTIAL TO TREAT PATIENTS IN DAYS

Treatment Journey

Source: Allogene data on file.

ALLOGENE IS CREATING THE AlloCAR T™ PRODUCT PLATFORM FOR TOMORROW

The Platform Opportunities. ALLO-329 - Autoimmune Diseases. Next generation dual CD19/CD70 CAR T to transform the treatment of. cema-cel - Heme Malignancies. Maximizing curative potential of CD19 CAR T by targeting MRD+ LBCL in 1L consolidation. ALLO-316 - Solid Tumors. Leverage propriety Dagger® technology to treat. All of these together make up AlloCAR T. The AlloCAR T Difference. Highly Scalable, Off-the-Shelf Product. One-Time Treatment. Simplified Logistics, Ideal for Community Clinicians. Ability to Leapfrog Competition. Vast Array of Potential Indications.

ELIMINATION OF TCR IN DONOR T CELLS MAY CONTROL GvHD

TCR in Donor T Cells
Elimination of TCR in Donor T Cells

ALLO-647: SELECTIVE LYMPHODEPLETION MAY DELAY GRAFT REJECTION

Host T Cell Recovery Delayed by Addition of Anti-CD52

Selective Lymphodepletion
MODULAR, FLEXIBLE DESIGN

MODULAR, FLEXIBLE DESIGN

Our modular, 136,000 square-foot facility was designed for growth. It currently has three production suites, with the ability to accommodate five as we look ahead to bringing new therapies onto the market.

IN-HOUSE QUALITY CONTROL AND TESTING

IN-HOUSE QUALITY CONTROL AND TESTING

We believe in the critical importance of understanding the quality of our investigational AlloCAR T™ products, which is why we operate the entire scope of product testing and maintain an open data strategy in-house.

COMMITMENT TO SUSTAINABILITY

COMMITMENT TO SUSTAINABILITY

Cell Forge 1 is a carbon-free facility that is fully powered by electricity, much of which will be delivered by the 2,400 solar panels on the rooftop. CF1 received LEEDv4 Interior Design and Construction Gold certification.

COLLABORATIVE DESIGN

COLLABORATIVE DESIGN

We included large windows throughout the facility to promote a culture of transparency and connection. Open workspaces, as well as the facility’s proximity to Allogene’s Headquarters, allow for regular cross-functional collaboration.

STATE-OF-THE-ART, IN-HOUSE MANUFACTURING FOR ON-DEMAND AlloCAR T™ PRODUCT AVAILABILITY

Allogene Building

Maintaining state-of-the-art, world-class manufacturing capabilities is at the core of our strategy to deliver readily available cell products faster, more reliably, and at greater scale. Our manufacturing facility, Cell Forge 1, located in Newark, California, in the eastern region of the San Francisco Bay Area, is designed for clinical and commercial manufacturing, analytical testing and distribution of cell products. This facility provides in-house quality assurance and quality control, per current good manufacturing practices (cGMPs), to ensure a reliable supply of AlloCAR T™ products for our clinical programs and commercial products, pending regulatory approval.

SCIENTIFIC PUBLICATIONS

CD19

December 2024

Alpha3: A Pivotal Phase 2 Study of First-Line Consolidation With Cemacabtagene Ansegedleucel (Cema‑Cel) in Patients With Large B‑Cell Lymphoma and Minimal Residual Disease After Response to Standard Therapy

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December 2023

Cellular Mechanisms Affecting Allogeneic CAR T Cell Expansion and Rejection in Large B-cell Lymphoma*

*In collaboration with The University of Texas MD Anderson Cancer Center.

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June 2023

Presentation, Durable Responses Achieved with Anti-CD19 Allogeneic CAR T ALLO-501/501A in Phase 1 Trials of Autologous CAR T-Naïve Patients with Relapsed/Refractory Large B-Cell Lymphoma (r/r LBCL)

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June 2023

Poster, Durable Responses Achieved with Anti-CD19 Allogeneic CAR T ALLO-501/501A in Phase 1 Trials of Autologous CAR T-Naïve Patients with Relapsed/Refractory Large B-Cell Lymphoma (r/r LBCL)

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June 2023

Poster, Phase 1 Results with Anti-CD19 Allogeneic CAR T ALLO-501/501A in Relapsed/Refractory Large B-Cell Lymphoma (r/r LBCL)

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June 2023

Presentation, Phase 1 Results with Anti-CD19 Allogeneic CAR T ALLO-501/501A in Relapsed/Refractory Large B-Cell Lymphoma (r/r LBCL)

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ALPHA Study

December 2021

ALPHA Study: ALLO-501 Produced Deep and Durable Responses in Patients with Relapsed/Refractory Non-Hodgkin’s Lymphoma, Comparable to Autologous CAR

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ALPHA2 Study

December 2021

ALPHA2 Study: ALLO-501A Allogeneic CAR T in LBCL, Updated Results Continue to Show Encouraging Safety and Efficacy with Consolidation Dosing

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First In Human Data of Allo 501A

June 2021

First-In-Human Data of ALLO-501A, An Allogeneic Chimeric Antigen Receptor (CAR) T Cell Therapy, and ALLO-647 in Relapsed/Refractory Large B Cell Lymphoma (R/R LBCL): ALPHA2 Study

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First In Human Data of Allo 501

May 2020

American Society of Clinical Oncology (ASCO) May 2020 – First-in-Human Data of ALLO-501 and ALLO-647 in Relapsed/Refractory Large B-cell or Follicular Lymphoma (R/R LBCL/FL): ALPHA Study

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CD19/CD70 Dual

November 2024

Preclinical Evaluation of ALLO-329: Allogeneic CD19 CAR T Cells Expressing an Anti-Rejection CD70 CAR for the Treatment of Autoimmune Diseases

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November 2023

Preclinical Evaluation of Allogeneic CD19 CAR T Cells Expressing an Anti-Rejection CD70 CAR

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CD70

November 2024

ALLO-316 in Patients With Advanced or Metastatic Clear Cell Renal Cell Carcinoma (ccRCC): Updated Safety and Efficacy From the Phase 1 TRAVERSE Multicenter Study

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April 2023

TRAVERSE: A Phase 1 Multicenter Study Evaluating the Safety and Efficacy of ALLO-316 in Patients with Advanced or Metastatic Clear Cell Renal Cell Carcinoma (ccRCC)

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April 2022

Preclinical Development and Evaluation of Allogeneic CAR T Cells Targeting CD70 for the Treatment of Renal Cell Carcinoma

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April 2022

Preclinical Development and Evaluation of Allogeneic CAR T Cells Targeting CD70 for the Treatment of Renal Cell Carcinoma

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Investigation of ALLO-316

December 2020

Investigation of ALLO-316: A Fratricide-Resistant Allogeneic CAR T Targeting CD70 As a Potential Therapy for the Treatment of AML

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American Association for Cancer Research

April 2019

American Association for Cancer Research (AACR) April 2019 – AlloCAR T™ Targeting CD70 For RCC

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Other Targets

November 2023

Preclinical Development and Characterization of Allogeneic CAR T Cells Targeting Claudin18.2 Positive Tumors

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August 2023

Constitutive Turbodomains Enhance Expansion and Antitumor Activity of Allogeneic BCMA CAR T Cells in Preclinical Models

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January 2023

Allogeneic CAR T Cells Targeting DLL3 Are Efficacious and Safe in Preclinical Models of Small Cell Lung Cancer

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January 2023

Allogeneic BCMA-Targeting CAR T Cells in Relapsed/Refractory Multiple Myeloma: Phase 1 UNIVERSAL Trial Interim Results

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December 2022

Poster, UNIVERSAL Updated Phase 1 Data Highlight Role of Allogeneic Anti-BCMA ALLO-715 Therapy for Relapsed/Refractory Multiple Myeloma

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December 2022

Presentation, UNIVERSAL Updated Phase 1 Data Highlight Role of Allogeneic Anti-BCMA ALLO-715 Therapy for Relapsed/Refractory Multiple Myeloma

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March 2022

Allogeneic Anti-BCMA CAR T Cells Are Superior to Multiple Myeloma-derived CAR T Cells in Preclinical Studies and May Be Combined with Gamma Secretase Inhibitors

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UNIVERSAL Updated Phase 1 Data Validates the Feasibility of Allogeneic

December 2021

UNIVERSAL Updated Phase 1 Data Validates the Feasibility of Allogeneic Anti-BCMA ALLO-715 Therapy for Relapsed/Refractory Multiple Myeloma

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Preclinical Evaluation of ALLO 605

December 2020

Preclinical Evaluation of ALLO-605, an Allogeneic BCMA TurboCAR T™ Cell Therapy for the Treatment of Multiple Myeloma

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First In Human Data of Allo 715

December 2020

First-in-Human Study of the Allogeneic Anti-BCMA ALLO-715 CAR T cell Therapy and the Anti-CD52 Mab ALLO-647 in Relapsed/Refractory Multiple Myeloma (UNIVERSAL Study)

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PLATFORM

November 2023

Preclinical Evaluation of Allogeneic CD19 CAR T Cells Expressing an Anti-Rejection CD70 CAR

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November 2023

Generation of Immune-Evasive Allogeneic CAR T Cells by Inactivation of the HLA Transcriptional Regulator RFX5 and Disruption of the Immune Synapse

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February 2023

Selective Targeting of Host CD70+ Alloreactive Cells With a CD70 Dagger™ Receptor to Prolong Allogeneic CAR T Cell Persistence

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November 2022

Generation of Hypoimmunogenic Allogeneic CAR T Cells by Inactivation of Transcriptional Regulators of HLA Class I and II Genes

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May 2022

Allogeneic CAR T Cells Derived From Younger Donor T Cells Have More Desirable T Cell Phenotype And Better in vitro Functionality

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PD1 TurboCAR T Cells

April 2021

PD1 TurboCAR™ T Cells: PD1-Resistant CAR T Cells With Programmable Cytokine Signaling Outputs

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June 2020 SMIC CAR T Cells

June 2020

American Association for Cancer Research (AACR) June 2020 – SMIC CAR T Cells: CAR T with Temporally-Controlled, Programmable Cytokine Signaling Outputs

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May 2020 TurboCAR T Cells

May 2020

American Society of Gene and Cell Therapy (ASGCT) May 2020 – TurboCAR™ T Cells: CAR T Cells with Constitutive, Programmable Cytokine Signaling Outputs

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Off the Shelf Allogeneic CAR T Cells

April 2020

Toward “Off-the-Shelf” Allogeneic CAR T Cells

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Safeguards for Chimeric Antigen Receptor T-Cell

June 2018

A Versatile Safeguard for Chimeric Antigen Receptor T-Cell Immunotherapies Valton J, Guyot V, Boldajipour B, et al.

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