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Takashi Yoshida and Tsutomu Hatano, Phytochemistry, November 2000, Volume 55, Issue 6, Pages 513529, doi:10.1016/S0031-9422(00)00232-6

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Treatment discontinuation rates in the ACHIEVE-1 study due to adverse events were 6% (orforglipron 3 mg), 4% (orforglipron 12 mg), and 8% (orforglipron 36 mg) vs

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Safety and Regulatory Differences Both BPC-157 and TB-500 carry similar broad regulatory characterizations - neither has FDA or EMA approval for human use, both are sold strictly as research chemicals for in vitro and animal-model investigation - but the specific regulatory facts differ

For mature cataracts, the effect rate was 80%