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After four months, many of the participants were able to tolerate small amounts of the foods they were allergic to, meaning an accidental exposure was no longer a life-threatening event

The regulatory gap reflects the fundamental difference in clinical evidence between the two compounds

That literature should not be dismissed, but neither should it be promoted as if it were a body of conclusive human clinical evidence

Interestingly, most people are deficient in vitamin B12, especially vegetarians or vegans, and persons with specific diseases

CagriSema submitted for FDA approval in December 2025 with expected approval in Q4 2026 or Q1 2027, meaning launch around mid-2027

What is the standard protocol