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Find Clinical Drug Pipeline Developments & Deals by Allogene Therapeutics
The net proceeds will be used to support the clinical development of ALLO-316, an AlloCAR T™ investigational product targeting CD70 in development for the treatment of advanced or metastatic renal cell carcinoma.
Under the agreement, Allogene will use Arbor’s proprietary CRISPR gene-editing technology in its next generation AlloCAR T platform, ALLO-329, for the treatment of autoimmune disease (AID).
ALLO-501A (cemacabtagene ansegedleucel) isbeing evaluated in clinical studies for the treatment of patients with Relapsed/Refractory Large B-Cell Lymphoma (LBCL).
ALLO-316, an AlloCAR T investigational product targets CD70, which is highly expressed in RCC. CD70 is also selectively expressed in several cancers, creating the potential for ALLO-316 to be developed across a variety of both hematologic malignancies and solid tumors.
The selection of ALLO-213 was based on potency and specificity against SCLC cell lines in vitro and in vivo, including cell lines with very low antigen density to establish sensitivity.
ALLO-715 is an anti-BCMA (B-cell maturation antigen) AlloCAR T therapy product candidate which is being developed as a potential novel treatment for multiple myeloma and other BCMA-positive malignancies.
UNIVERSAL is the first trial to demonstrate significant responses can be achieved with an allogeneic CAR T product candidate. ALLO-715, an anti-BCMA AlloCAR T product candidate for relapsed/refractory multiple myeloma.
CAR T Together™ is a first-of-its-kind effort representing the many investigators who are committed to supporting the development of “off-the-shelf” (allogeneic) CAR T products that are scalable and faster to deliver – making treatments accessible to more cancer patients.
ALPHA2 Trial, Evaluating ALLO-501A in Relapsed/Refractory Large B Cell Lymphoma Patients, is Designed to Leverage the Ease and Convenience of a Single Dose of ALLO-501A.
ALLO-605 is the Company’s first TurboCAR™ product candidate. TurboCAR™ is a proprietary, next generation platform technology based on a programmable cytokine signaling, designed to control T cell exhaustion and to improve T cell function and potency.
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