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Discontinuation due to adverse events was 5.9% across CT-388 treatment arms and 1.3% in the placebo arm, with no new or unexpected safety signals reported

Inject Semaglutide: Pinch a fold of skin at the injection site

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This study was conducted as a part of regulatory commitment however, with the increased utilization of the FDC, comprehensive reporting of real-world data can be generated providing further evidence on the efficacy and tolerability of the FDC in the Indian population