Lentiviral vectors offer gene therapy option for hemophilia A patients with anti-AAV antibodies
Research led by Christian Medical College in Vellore, India, has demonstrated the successful use of lentiviral vectors to ...
Indian scientists develop novel gene therapy treatment for haemophilia
Indian scientists successfully use gene therapy to treat severe haemophilia A, a rare hereditary condition with promising ...
MedPage Today2d
Lentiviral Gene Therapy Shows Promise in Severe Hemophilia A
SAN DIEGO -- Results from a small single-center study showed that treatment with a gene therapy involving the use of ...
FierceBiotech22d
Novartis taps Vyriad’s viral vectors to develop in vivo T cell editing
Vyriad’s lentivirus vectors target T cells within a patient’s body and deliver genes coding for chimeric antigen receptors. Once the T cells decipher those genetic instructions, they are ...
EurekAlert!24d
A new strategy to enhance gene therapy for sickle cell disease
Click here to read the article now. Anne Galy, PhD, from Inserm, and coauthors, applied a novel lentivirus-based gene therapy strategy in CD34+ hematopoietic progenitor and stem cells (HSPCs ...
The New England Journal of Medicine27d
NEJM at AHA — Left Atrial Appendage Closure after Ablation for Atrial Fibrillation
In this audio interview, Editor-in-Chief Eric Rubin and Deputy Editor Jane Leopold discuss research being presented at the 2024 American Heart Association Scientific Sessions.
The New England Journal of Medicine27d
NEJM at AHA — Tirzepatide for Heart Failure with Preserved Ejection Fraction and Obesity
In this audio interview, Editor-in-Chief Eric Rubin and Deputy Editor Jane Leopold discuss research being presented at the 2024 American Heart Association Scientific Sessions.