Idiopathic Pulmonary Fibrosis

Idiopathic pulmonary fibrosis (IPF)

 is a progressive fibrotic lung disease of unknown cause. It remains incurable and has a poor prognosis for many patients, with a median survival of 3-5 years from diagnosis.

 For more information on our current and past study involvement, please follow the links to the left (* indicates Bristol led).

Studies & trials

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