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The product is a compounded buccal-dissolve formulation it is not FDA-approved, and the company received an FDA warning letter on February 20, 2026 over labeling and marketing claims

AEs leading to trial product discontinuation occurred in 6/90 (7%) participants in the CagriSema 2.4 mg/2.4 mg group, 11/93 (12%) participants in the CagriSema 1 mg/1 mg group, and 1/91 (1%) in the placebo group

Email-only contact during disputes frustrates members who want to speak with a human being

Such an approach, if done under mild conditions, could be an alternative to other kinds of hair dyes, avoiding some of the toxicity or allergies associated with those chemicals, said head researcher Nathan Gianneschi

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