Bharat Biotech invests $75 million in India's first Cell & Gene Therapy facility, focusing on advanced therapies and ...
Dr. Raches Ella, Chief Development Officer, Bharat Biotech, spearheading this CGT initiative, said that oncology and rare ...
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GlobalData on MSNAllogeneic cell therapies “poised for prime time” says expertWhile the allogeneic vs autologous debate continues in the cell therapy field, research on in vivo therapies is drawing ...
Our Bureau, Bengaluru Thursday, March 20, 2025, 17:40 Hrs [IST] ...
In a groundbreaking advancement for families grappling with the challenges of Dravet syndrome, a rare and life-altering form of epilepsy, scientists have developed a new gene replacement therapy in ...
After bringing Zolgensma to market in 2019 as the first gene therapy for spinal muscular atrophy, Novartis is back with a ...
By replacing the defective gene associated with Dravet syndrome in mice, scientists successfully alleviated symptoms without side effects.
A single piece of genetic material influences whether someone develops type 1 diabetes, Dutch researchers discovered. People ...
REGIONS NEWS FDA priority review of pz-cel Biologics License Application (BLA) progressing with Prescription Drug User Fee ...
Gene expression testing helps determine chemotherapy needs for hormone receptor-positive breast cancer, optimizing treatment ...
FDA granted priority review to Company's BLA for PRGN-2012 for the treatment of adults with recurrent respiratory papillomatosis and set PDUFA target action date ...
A self-made millionaire has made significant lifestyle changes to boost his health, wellbeing and fitness in a bid to live to ...
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