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US FDA grants saracatinib Orphan Drug Designation for idiopathic pulmonary fibrosis

18 March 2019

The US Food and Drug Administration (FDA) has granted Orphan Drug Designation (ODD) for saracatinib, a potential new medicine for the treatment of idiopathic pulmonary fibrosis (IPF), a type of lung disease that results in scarring (fibrosis) of the lungs. Saracatinib is an inhibitor of src kinase which regulates broad cell functions including cell growth and cell differentiation. Saracatinib has completed Phase I development.

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