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Adjustments to the protocol The sponsor engaged an independent nonprofit organization to organize and conduct virtual interviews with participants with early-stage symptomatic AD and care partners to gain their preferences about study conduct that could be reflected in the protocol
A., DAlessio, D
doi: 10.2337/dc20-1558 39 CaiTHuYDingBYanRLiuBCaiLet al
Results of a pilot study
Dose Adjustment Based on Monitoring Inadequate subjective response and IGF-1 increase 80 ng/mL represents ideal efficiency
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