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Pharmacokinetic analysis revealed it to be orally active with significantly increased metabolic stability, exhibiting a plasma half-life of 335.5 minutes, allowing for prolonged systemic availability [2]

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[DOI] [PubMed] [Google Scholar] 67.Mercadal L., Coudert M., Vassault A., Pieroni L., Debure A., Ouziala M., Depreneuf H., Fumeron C., Servais A., Bassilios N., et al

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performed a systematic review to describe the type of markers of oxidative stress identified in different biological specimens of patients with IPF [142]