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Our latest news
Dan Williams interviewed for leading podcast, Beyond Biotech
Jul 11, 2024
Leading biotech appoints senior industry figure as Chief Medical Officer to define clinical strategy and oversee trials
Jun 10, 2024
In a major article, Dan Williams considers how to overcome obstacles in rare disease treatment
Jun 10, 2024
SynaptixBio awarded second FDA Orphan Drug Designation to boost search for rare disease therapies
Apr 29, 2024
Bioscience Today features major Dan Williams article about collaboration driving rare disease drug development
Apr 29, 2024
Dan Williams says Big Pharma could help accelerate market introduction for rare disease drugs
Apr 28, 2024
Dan Williams interviewed for prestigious journal - Major International Clinical Trials feature showcases SynaptixBio story
Dec 23, 2023
SynaptixBio awarded prestigious Innovate UK grant to expand search for rare disease therapies
Dec 23, 2023
Leading biotech firm welcomes new NHS rapid diagnostic service for rare diseases, but says wider newborn screening is key
Dec 23, 2023
BBC features TUBB4A leukodystrophy case study – Dan Williams contribution highlights lack of widespread awareness of rare diseases
Dec 23, 2023
Oxford biotech firm secures £13.2m to develop first treatment for rare, incurable, deadly disease.
Apr 27, 2023
SynaptixBio agrees US children’s hospital deal to develop world’s first treatment for deadly disease
Mar 4, 2023
We were delighted to welcome Sky News to Oxfordshire in November
Mar 3, 2023
‘Time running out’ in teen girl’s battle with TUBB4a leukodystrophy
Mar 2, 2023
British biotech firm secures FDA rare paediatric disease designation
Feb 9, 2023
Children with undiagnosed conditions urged to get checked for rare, incurable and deadly disease
Jan 8, 2023
The powerful story of Frankie Sheridan-Hill, aged seven, featured on ITV
Nov 2, 2022
Thousands of patients could have rare life-threatening diseases without knowing it, experts warn
Feb 7, 2022
Mum diagnoses daughter's rare life-threatening disease
Oct 1, 2021
New biotech firm launched to develop ‘revolutionary’ treatment for one of world’s rarest diseases
Aug 18, 2021
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