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2102, 2023

Weill Cornell study demonstrates safety of intravenous administration of an AAV8 gene therapy

February 21st, 2023|Gene & Cell Therapy Testing, News|

Researchers report on the safety of a gene therapy to treat the common autosomal recessive hereditary disorder alpha 1-antitrypsin (AAT) deficiency in a new article in the peer-reviewed journal Human Gene Therapy. In ATT deficiency, neutrophil proteases destroy the lung parenchyma, the portion of the lungs...

702, 2023

FDA clears Sana Biotechnology’s CAR T Therapy IND application for patients with B-cell malignancies

February 7th, 2023|Gene & Cell Therapy Testing|

The goal of the hypoimmune platform is to overcome the immunologic rejection of allogeneic cells, which if true for SC291 may result in longer CAR T cell persistence and a higher rate of durable complete responses for patients with B-cell lymphomas or leukemias. The hypoimmune platform includes disruption of major...

1701, 2023

Scientists develop novel mRNA delivery method using extracellular vesicles

January 17th, 2023|mRNA therapeutics|

In the study, published in Nature Biomedical Engineering, researchers from MD Anderson Cancer Center use EV-encapsulated mRNA to initiate and sustain collagen production for several months in the cells of photoaged skin in laboratory models. It is the first therapy to demonstrate this ability and represents a proof-of-concept for deploying the EV mRNA therapy...

1312, 2022

ASGCT Members Provide Recommendations During FDA Liaison Meeting

December 13th, 2022|Gene & Cell Therapy Testing|

ASGCT held its fifth annual liaison meeting with FDA CBER’s Office of Tissues and Advanced Therapies (OTAT) on Nov. 14, 2022. A group of Society leaders and members gave two presentations to FDA on significant topics in the field, followed by a presentation from FDA. Dr. Keith Wonnacott, ASGCT’s Regulatory Affairs Committee Chair, chaired the meeting and moderated discussion...

612, 2022

CG Oncology advancing clinical-stage urologic oncology immunotherapy pipeline

December 6th, 2022|Gene & Cell Therapy Testing, News|

Company files its first Investigational New Drug application for its lead program KYV-101, a novel fully human CD19 CAR T-cell therapy, for the treatment of lupus nephritis. Kyverna’s therapeutic platform combines advanced T-cell engineering and synthetic biology technologies to suppress and eliminate...

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