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Study J: TRESIBA Administered at the Same Time Each Day in Combination with a Rapid-Acting Insulin Analog at Mealtimes in Pediatric Patients 1 Year of Age and Older The efficacy of TRESIBA was evaluated in a 26-week, randomized, open label, multicenter trial in 350 patients with type 1 diabetes mellitus (Study J)
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Following this, the Food and Drug Administration (FDA) gave other pharmaceutical companies permission to make non-branded, compounded versions of the drugs, using the active ingredient, semaglutide
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