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Description
Safety data indicate mostly mild gastrointestinal events (nausea, diarrhea, vomiting), dose-dependent, and often improved with titration
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5 The rule requires the submission of baseline or demographic characteristic measured in the clinical trial, including age, sex/gender, race, ethnicity (if collected under the protocol) for trials that are required to be registered under Section 11.22 (Phase 1 trials are excluded), 6 for reporting purposes via ClinicalTrials.gov
