Home Breaking Boundaries: Accelerating Antibody Discovery and Development for In Vivo CAR-T

Breaking Boundaries: Accelerating Antibody Discovery and Development for In Vivo CAR-T

Nov 19, 2025 09:44 CST Updated 09:45
Vivacta

Cell Therapy Researcher

On November 4, Professor Jennifer Doudna, the 2020 Nobel Prize in Chemistry laureate, led her team to secure $82 million in funding for development.in vivoCAR-T. On November 5, in Chinain vivoCAR-T Newcomer IVACTA Biotechnology Completes Angel Round Financing of Over 100 Million RMB. From Overseas to China,in vivoCAR-T has achieved "two-way success" in the global market, with the industry's popularity visibly climbing.


In vivoCAR-T, namely in vivo CAR-T technology, does not require the collection of a patient's autologous T cells for ex vivo modification like traditional ex vivo CAR-T. Instead, it directly delivers the CAR gene to T cells in the body via a vector, transforming them in situ into CAR-T cells to exert therapeutic effects. Compared with traditional autologous CAR-T therapy, in vivo CAR-T offers advantages such as simpler manufacturing, lower costs, no need for lymphocyte depletion, and the possibility of repeated dosing. It is expected to become a new paradigm for "off-the-shelf" cell therapy, especially suitable for solid tumors, immunodeficient patients, and time-sensitive treatment scenarios. This technological breakthrough overcomes the bottlenecks of long preparation cycles, high costs, and reliance on specialized manufacturing centers associated with traditional therapies, significantly improving accessibility.


Despite the fact that in vivo CAR-T is still in the early stages of research and clinical trials, facing challenges such as targeting specificity, delivery efficiency, and safety (e.g., cytokine release syndrome), it represents a significant direction for the next generation of immunotherapy, with tremendous potential to treat hematologic malignancies and even solid tumors, as well as other disease scenarios (autoimmune diseases, rare diseases, etc.).


In order to acceleratein vivoDevelopment of CAR-T Therapy, PharmRing and IVACTA Biotechnology jointly invitedDerek Chen, Senior Director of IVACTA Biotechnology's Antibody Drug Discovery Department, and Ying Li, Director of IVACTA Biotechnology's Antibody PD Department, onNovember 26Arrive at the Yaoke Rongyun Live Broadcast Room, fromin vivoCAR-T Begins to Enter the World of Antibodies.


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Derek Chen

Senior Director of Antibody Drug Discovery at IVACTA Biotechnology

Derek Chen is the Senior Director of the Antibody Drug Discovery Department at IVACTA Biotechnology. After obtaining his Ph.D. in Immunology from the University of Massachusetts Medical School, he joined GenScript in 2015. Over the past seven years, he has been in charge of the antibody drug discovery platform, with experience in over 200 projects involving antibody drug discovery and engineering optimization, as well as three related patents in the field of biopharmaceutical discovery.


Ying Li

Director of PD Department, IVACTA Biotechnology Antibody

Ying Li obtained a Ph.D. in Chemical Engineering from Pennsylvania State University, focusing on the research of membrane separation and purification of biomacromolecules during this period. From 2017 to 2022, Ying Li worked at the U.S. headquarters of Merck Millipore as a Research and Development Manager, responsible for developing the company’s continuous flow antibody and gene therapy viral vector purification process platforms. In 2022, Ying Li joined IVACTA Biotechnology as the Director of Antibody Process Development. To date, Ying Li has led the team to complete the process development of more than 10 CMC projects, obtaining 6 FDA/NMPA IND approvals, and has led the R&D of IVACTA Biotechnology's Toolbox and AXC technology platforms.Ying LiCommitted to innovation in the field of bioprocessing, published 9 academic papers in top-tier journals in the field, and was honored as a national-level overseas high-level young talent in 2023.



AboutIVACTA Biotechnology

ProBio is committed to providing one-stop CDMO services for biotechnology and pharmaceutical companies, helping global clients accelerate the drug development process with services ranging from clinical trials to commercial production. ProBio always adheres to the principle of "Quality First, Innovation-Driven" and collaborates with biotechnology companies worldwide to expedite the delivery of advanced therapies to meet patient needs.

For more information and cooperation methods, please visit www.probiocdmo.cn



About PharmaCircle

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