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As monotherapy , a multicentre, randomised, double-blind, placebo-controlled and active-controlled Phase 2 dose-finding trial enrolled 706 adults with overweight or obesity (without diabetes) to once-weekly subcutaneous cagrilintide across doses of 0.3 to 4.5 mg over 26 weeks

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these are trial protocols only, as no licensed dosing schedules or UK SmPCs exist for either agent

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The secondary plot for the first k obs values from the second phase yielded a rate contant at GSSG saturation around 10 s 1 for all three PfGrx variants (Fig