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Could an existing antibiotic be used to treat rare liver disease?
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Celebrating 2 years of the network driving innovation for people with CF
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New £6m fellowship programme to help rare disease discoveries reach patients faster
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What makes cystic fibrosis research such a rewarding career?
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7 lessons from our childhood cancer workshops
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New study brings hope for children with rare life-threatening kidney disease
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Introducing Raremap: a new way to navigate the rare disease landscape
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LifeArc-founded RQ Bio secures £85.5 million to advance long-acting antibody for influenza prevention
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New boost for personalised rare disease treatments as the Rare Therapies Launch Pad becomes part of LifeArc
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World-first gene therapy to target devastating rare immune disorder
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LifeArc announces partnership with Elpida Therapeutics to accelerate gene therapies for ultra-rare diseases in children
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LifeArc Translational Science Summit 2026: Charting new paths for rare disease
