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10.1038/sj.bjp.0706739 171 KraftR.GrimmC.GrosseK.HoffmannA.SauerbruchS.KettenmannH.et al (2004)

In the controlled trial in pediatric patients ages 13 to 17 years (Study 4), 3% (7/233) of VYVANSE-treated patients discontinued due to adverse reactions compared to 1% (1/77) of placebo-treated patients

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Treatment of BPC 157 was administered orally in drinking water, topically via a thin cream and via intraperitoneal administration over a 90-day period

[DOI] [PMC free article] [PubMed] [Google Scholar] 6.Liyanage T., Toyama T., Hockham C., Ninomiya T., Perkovic V., Woodward M., Fukagawa M., Matsushita K., Praditpornsilpa K., Hooi L.S., et al