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These tests are typically used only in clinical trial settings, pharmacokinetic studies, or specialized research environments to measure drug concentrations and assess bioavailability
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)
Brown, M.J
Dose: 0.51 mg per day , subcutaneous Frequency: 35 times weekly Cycle: 8 weeks on / 4 weeks off , repeated indefinitely Stack: commonly run alongside NAD+ infusions and CJC-1295 / Ipamorelin for full anti-ageing coverage
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