Obe-cel (obecabtagene autoleucel, AUTO1) is a CD19 CAR T cell investigational therapy designed to overcome the limitations in clinical activity and safety compared to current CD19 CAR T cell therapies. Designed to have a fast target binding off-rate to minimize excessive activation of the programmed T cells, obe-cel may reduce toxicity and be less prone to T cell exhaustion, which could enhance persistence and improve the ability of the programmed T cells to engage in serial killing of target cancer cells. In collaboration with our academic partner, UCL, obe-cel is currently being evaluated in a Phase 1 clinical trial in B-NHL. The company has also progressed obe-cel into the FELIX study, a potential pivotal study in adult ALL.
Obe-cel has been granted orphan drug designation by the FDA, PRIME designation in relapsed/ refractory B-ALL by EMA and ILAP designation by the MHRA in adult relapsed/ refractory ALL.
AUTO1/22 is a novel dual targeting CAR T cell based therapy candidate based on obe-cel. It is designed to combine the enhanced safety, robust expansion & persistence seen with the fast off rate CD19 CAR from obe-cel with a high sensitivity CD22 CAR to reduce antigen negative relapses. This product candidate is currently in a Phase 1 clinical trial for patients with r/r paediatric ALL.
AUTO4 and AUTO5 are two programmed T cell therapies for the treatment of peripheral T-cell lymphoma targeting TRBC1 and TRBC2 respectively, and both employing a novel and differentiated treatment approach. Each are designed to selectively kill cancerous T cells in a manner that we believe will preserve a portion of the patient’s normal, healthy T cells to maintain immunity.
Since the uses a novel mechanism to target T cells, Autolus has also programmed the product candidate with the RQR8 “safety switch” in order to allow physicians to manage toxicity by eliminating the programmed T cells if a patient experiences severe adverse side effects from the treatment. AUTO4 is currently being tested in a Phase 1 study in TRBC1-positive peripheral T cell lymphoma.
A programmed T cell therapy targeting GD2 in development for the treatment of neuroblastoma, osteosarcoma and SCLC.
A Phase 1 clinical trial with AUTO6 was sponsored and conducted by Cancer Research UK, or CRUK, and data demonstrated initial anti-tumor activity in this solid tumor indication.
Autolus is developing AUTO6NG, a next generation programmed T cell product candidate which is in pre-clinical development. AUTO6NG builds on preliminary proof of concept data from AUTO6. AUTO6NG incorporates additional cell programing modules to overcome immune suppressive defense mechanisms in the tumor microenvironment, in addition to endowing the CAR T cells with extended persistence capacity.
AUTO8 is our next-generation product candidate for multiple myeloma which comprises two independent CARs for the multiple myeloma targets, BCMA and CD19. We have developed an optimized BCMA CAR which is designed for improved killing of target cell that express BCMA at low levels. This has been combined with fast off rate CD19 CAR from obe-cel.
We believe that the design of AUTO8 has the potential to induce deep and durable responses and extend the durability of effect over other BCMA CARs currently in development.