Integrated gene therapy successfully treated Haemophilia A in India, providing long-term relief without bleeding episodes for ...

Gene therapy for haemophilia A using Roctavian and lentivirus vector shows promise in treating the rare, hereditary condition ...

Results from a small single-center study showed that treatment with a gene therapy involving the use of lentiviral ...

Research led by Christian Medical College in Vellore, India, has demonstrated the successful use of lentiviral vectors to ...

BHUBANESWAR: In a significant medical breakthrough, India’s first human gene therapy with a lentiviral vector for severe ...

Landmark publication in leading ophthalmology research journal demonstrates the power of 4DMT’s Therapeutic Vector Evolution platform to invent ...

HALT, pairs Amarna’s SV40-derived gene delivery vector platform with Phenocell’s in vitro AMD disease model, which accurately ...

From reprogrammed stem cells to next-generation gene editing, 2024 has seen some incredible developments with the potential ...

Indian scientists successfully use gene therapy to treat severe haemophilia A, a rare hereditary condition with promising ...

Physician-researchers with City of Hope have developed a way to add features to T cells to help them overcome mechanisms of ...

AAV is the only non-pathogenic viral vector now available and has been used successfully in establishing long-term gene expression without substantial immune response or toxicity in both dividing ...

Flagship CEO-partner and Ring CEO Tuyen Ong, M.D., will also be shifting to an advisory role in the new year, according to ...