Medically reviewed by Steffini Stalos, DO Hemophilia disease is a rare inherited bleeding disorder. People with this genetic ...

“Gene therapy for hemophilia A with the use of lentiviral vector-transduced autologous HSCs resulted in stable factor VIII ...

Still, Novo is steadfast in its goal to eventually become a leader in the space, the company’s EVP of rare disease, Ludovic ...

Researchers at the Francis Crick Institute have identified genetic changes in blood stem cells from frequent blood donors that support the production of new, non-cancerous cells.

Despite a large portion of the Rs 91 crore budget remaining unspent, the State Health Coordinator has requested additional ...

Pfizer discontinuing Beqvez once again highlights the struggles pharma companies have in keeping cell and gene therapies ... a protein that helps blood clot. Haemophilia B patients lack the ...