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Phase III clinical data from SCENESSE trials (the FDA-approved formulation of afamelanotide) demonstrated that patients with erythropoietic protoporphyria achieved clinically meaningful photoprotection after 60 days of sustained drug delivery via controlled-release implant

For CJC-1295, the Jett study documented mild flushing and a single episode of vasovagal syncope out of 65 subjects [2]

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All chemical reagents used in this study were of analytical grade

We also source our peptides directly from vetted California-based labs that adhere to the highest safety and quality standards