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The current certification is valid through December 31, 2027

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Updates to the Interim 503A Bulks List On the same day, the FDA republished its interim 503A Bulks List with updates

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All study participants were randomly assigned to an experimental treatment group that received subcutaneous injection of cagrilintide, once-weekly, in doses of either 0.3, 0.6, 1.2, 2.4, or 4.5 mg, as well as a one-daily 3.0 mg dose of liraglutide, and a volume matched placebo for control purposes

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That said, because large-scale, long-term human trials are limited, its complete safety profile is not yet fully understood

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Injections may also be recommended for those who have had bariatric surgery or other conditions affecting digestion

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