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Open-label extension ACCESS Participants who completed the double-blind treatment period on study drug (or placebo) and signed informed consent ( n = 151) were eligible to enroll in the ACCESS OLE to assess the longer-term safety of aleniglipron, durability and maintenance of weight loss for an additional planned 36 weeks (from weeks 36 to 72)
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Numerous factors, including study design, demographic characteristics, length of intervention, CGM devices, AID algorithms, and insulin pumps, may be contributing to this
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