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CagriSema FDA approval timeline Novo Nordisk submitted the New Drug Application (NDA) to the FDA on December 18, 2025 , for chronic weight management in adults with obesity or overweight with a weight-related comorbidity

According to publicly available data it remains an experimental molecule in December 2025 a registration dossier for weight management was submitted to the US FDA, but to date CagriSema holds no registration

HUBERMAN: Again, that's drinkelement.com slash Huberman

Thus, cobalamin deficiency has been reported with regional enteritis, Whipple disease, ileal tuberculosis, tropical sprue, and surgical resection of the distal ileum, among other conditions

They only partner with FDA pharmacies, the provider told me, and she gave me the name of the pharmacy that would be compounding my peptides

4) B12d.org organises interesting online talks