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Most adverse events were mild to moderate gastrointestinal events, primarily occurring during the dose-escalation period
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[DOI] [PMC free article] [PubMed] [Google Scholar] 49.Kuo T.T., Chen Y.H., Wang V., Huang E.Y., Ma K.H., Greig N.H., Jung J., Choi H.I., Olson L., Hoffer B.J., et al
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