Nobel Prize-Winning Science applied to ATTR Amyloidosis
A groundbreaking study in ATTR amyloidosis, using novel CRISPR/Cas9, has dosed the first patient in the UK. This revolutionary technology brings us a step closer to the dream of curing inherited diseases like hereditary amyloidosis. (more…)
Amyloidosis Forum launches series meetings on novel endpoints and clinical trial design
The Amyloidosis Forum has launched a series of virtual meetings to focus on Novel Endpoints and Analyses for Clinical Trials in AL amyloidosis. The first meeting of the series took place on October 15th, 2020. The meeting was held...