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Patients meeting the inclusion/exclusion criteria were randomized in a 2:1 ratio to receive a 2 mg dose of EGRIFTA (1 mg/vial formulation) or placebo subcutaneously daily for 26 weeks

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The differential is not marginal it is the difference between a compound that ran a full clinical program and failed to prove efficacy, and one that has demonstrated both efficacy and cardiovascular benefit in some of the largest obesity trials ever conducted

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