Expanding the Use of CAR T Therapy With shRNA

Video

The chief executive and chief medical officers of Celyad Oncology discussed the company’s future research and plans.

Celyad Oncology is targeting cancers with a number of allogeneic CAR T-cell therapies. Their lead program, CYAD-211, is currently being evaluated in the phase 1 IMMUNICY trial (NCT04613557).

Celyad presented positive interim data at the European Hematology Association (EHA) 2021 Congress in June 2021 from IMMUNICY that showed dose-dependent engraftment up to dose level 3 of 300 x 106 cells per infusion. 

The company reported that no graft-versus-host disease, dose-limiting toxicities, or CAR T-cell related encephalopathy syndromes have occurred to date. A partial response was seen in 2 of the 5 evaluable patients. CYAD-211 cells were detected by polymerase chain reaction-based methods in all 6 patients with evidence of a dose-dependent increase in cell engraftment.

GeneTherapyLive spoke with Filippo Petti, chief executive officer and chief financial officer, and Charles Morris, MBBS, chief medical officer, Celyad Oncology, about the company's future plans and upcoming research. They also discussed potential future opportunities for their short hairpin RNA platform.

REFERENCE
Celyad Oncology presents updates on allogeneic CAR T clinical candidates and shRNA-based preclinical concepts at research & development day. News release. Celyad Oncology. July 20, 2021. https://www.businesswire.com/news/home/20210720005854/en/Celyad-Oncology-Presents-Updates-on-Allogeneic-CAR-T-Clinical-Candidates-and-shRNA-based-Preclinical-Concepts-at-Research-Development-Day
Recent Videos
Chun-Yu Chen, PhD, a research scientist at Seattle Children’s Research Institute
William Chou, MD, on Targeting Progranulin With Gene Therapy for Frontotemporal Dementia
Alexandra Collin de l’Hortet, PhD, the head of therapeutics at Epic Bio
David Dimmock, MBBS, on Accelerating Therapy Discovery and Approval With AI David Dimmock, MBBS, on Accelerating Therapy Discovery and Approval With AI
Joshua M. Hare, MD, on Working to Address Unmet Needs in Alzheimer Disease With Lomecel-B Cell Therapy
John Finn, PhD, the chief scientific officer of Tome Biosciences
David Dimmock, MBBS, on a Promising Case Study of Ultra-Rare, AI-Guided, ASO Development
William Chou, MD, on Expanding Frontotemporal Dementia Gene Therapy to Both GRN and C9orf72 Mutations
Scott Jeffers, PhD, on The Importance of Precise Reproducibility of AAVs
© 2024 MJH Life Sciences

All rights reserved.