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Dec 23, 2023
SynaptixBio awarded prestigious Innovate UK grant to expand search for rare disease therapies
SynaptixBio awarded prestigious Innovate UK Grant. BioMedical Catalyst grant supports expanded search for rare disease therapies
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Apr 28, 2023
Oxford biotech firm secures £13.2m to develop first treatment for rare, incurable, deadly disease.
A pioneering biotech firm has secured £13.2 million to fund its mission to develop the world’s first treatment for a rare, incurable and...
419 views

Feb 9, 2023
British biotech firm secures FDA rare paediatric disease designation
British biotech firm secures FDA rare paediatric disease designation in bid to develop world’s first treatment for incurable, deadly disease
210 views


Jan 8, 2023
Children with undiagnosed conditions urged to get checked for rare, incurable and deadly disease
Children with undiagnosed conditions urged to get checked for rare, incurable and deadly disease
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Nov 12, 2022
We were delighted to welcome Sky News to Oxfordshire in November
We were delighted to welcome Sky News to Oxfordshire in November
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Nov 2, 2022
The powerful story of Frankie Sheridan-Hill, aged seven, featured on ITV
The powerful story of Frankie Sheridan-Hill, aged seven, featured on ITV
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Oct 16, 2022
SynaptixBio agrees US children’s hospital deal to develop world’s first treatment for deadly disease
Biotech firm enters into a pioneering new licence agreement in bid to develop world’s first treatment for deadly disease
225 views


Sep 8, 2022
‘Time running out’ in teen girl’s battle with TUBB4a leukodystrophy
‘Time running out’ in teen girl’s battle with TUBB4a leukodystrophy
495 views

Feb 7, 2022
Thousands of patients could have rare life-threatening diseases without knowing it, experts warn
Thousands of patients could unknowingly suffer with a rare life-threatening disease, experts have warned. TUBB4a leukodystrophy - an...
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Sep 30, 2021
Mum diagnoses daughter's rare life-threatening disease
Mum diagnoses daughter's rare life-threatening disease
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Aug 17, 2021
New biotech firm launched to develop ‘revolutionary’ treatment for one of world’s rarest diseases
New biotech firm launched to develop ‘revolutionary’ new treatment for one of world’s rarest neurodegenerative diseases
98 views
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