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Gastrointestinal adverse events (affecting 79.6% in the cagrilintidesemaglutide group and 39.9% in the placebo group), including nausea, vomiting, diarrhea, constipation, or abdominal pain, were mainly transient and mild-to-moderate in severity

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Thus, at non-procurement agencies such as the National Institutes of Health (NIH) and the National Science Foundation (NSF), Phase III is typically taken to mean the commercial take-up of SBIR-funded technologies

What is GACLIV Injection