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The CagriSema combination is in Phase 3 trials (REDEFINE program) in the EU/USA, with approval expected 20272028

Most patients experience no adverse effects, and when present, theyre typically mild and transient including temporary digestive changes as the gut adjusts, minor nausea (usually resolving within days), or altered bowel patterns during initial therapy

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BPC-157 is not on the FDA's approved drug list, but the bulk active ingredient is permitted for compounding by a 503A pharmacy under Section 503A of the Federal Food, Drug, and Cosmetic Act

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