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Throughout the 0-32 week treatment period, adverse outcomes and the occurrence of anti-cagrillintide antibodies were assessed in addition to any changes in systolic and diastolic blood pressure, pulse rate, plasma high-sensitivity C-reactive protein, aldosterone, and the activity of renin
Current trial status and protocol details can be verified via ClinicalTrials.gov , the EU Clinical Trials Information System (CTIS) , or the ISRCTN registry
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The full barrel of a 1mL syringe = 100 units
