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Yusta B, Baggio LL, Koehler J, et al
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Available Strength:0.25mg + Sharps Bin + GP Consultation
Post hoc subgroup analyses were conducted to determine if the efficacy observed in this patient population was consistent with the SELECT trial, and therefore the enrolment criteria for this subgroup replicated that of the SELECT trial (i.e., limiting the subpopulation to patients with prior MI, stroke [excluding TIA], and/or PAD) with a BMI criterion of 27 kg/m 2 or higher
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