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British biotech firm secures coveted FDA designation in bid to develop world's first treatment for rare, incurable and deadly disease - Vimarsana News

British biotech firm secures coveted FDA designation in bid to develop world's first treatment for rare, incurable and deadly disease

A leading UK biotech firm founded to develop the world’s first treatment for a rare, incurable and deadly disease has secured its first Food and Drug Administration (FDA) designation. SynaptixBio, which aims to tackle TUBB4a leukodystrophy – a genetic and debilitating condition which mainly affects babies and ...

$1.5 million grant going to Hormel Institute research on cause of incurable diseases - Vimarsana News

$1.5 million grant going to Hormel Institute research on cause of incurable diseases

'This grant will provide a pathway to bridge basic and clinical research and open up new directions in working with scientists...'

Source: kimt.com
Bluebird wins FDA approval of gene therapy for rare brain disorder - Vimarsana News

Bluebird wins FDA approval of gene therapy for rare brain disorder

BioPharma

CHOP Family from Vermont Helps Raise Awareness for Leukodystrophy - Vimarsana News

CHOP Family from Vermont Helps Raise Awareness for Leukodystrophy

Adeline Vanderver, MD Beth Leduc wasn’t expecting her son Christian to be diagnosed with leukodystrophy. Now, she’s making sure other families in