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All these studies are in early stages, but recently released data for a 12-week phase 2 study of the v1/v6 inhibitor in 67 patients with idiopathic pulmonary fibrosis showed no significant on-target toxicity and an apparent dose dependent efficacy in slowing the rate of loss of lung function and progression of radiographic evidence of fibrosis

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albicans may express either hydrophilic or hydrophobic surface proteins (Singleton and Hazen, 2004)