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As of October 2019, MT-I is approved by the United States Food and Drug Administration (FDA) under the brand name Scenesse for increasing tolerance to sunlight and reducing pain caused by ultraviolet light (UV-light) exposure in patients with erythropoietic protoporphyria (EPP)

Other plans include testing combinations of anti-cancer drugs in the context of dietary changes that could improve cancer outcomes

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Starting conservative rather than titrating up aggressively is the single biggest lever you have over how noticeable this side effect gets

10.1210/endo-127-5-2217 45 LeiS.ClydesdaleL.DaiA.CaiX.FengY.YangD.et al (2018)