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Dihexa has compelling preclinical data, unprecedented receptor potency, and zero human clinical trials

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Table 1 Global Response Assessment Scale Number Response Grading (%) Outcome 1 Significantly worse 0 Failure of the therapy 2 Somewhat worse 1 to 25 Failure of the therapy 3 Unchanged (neither worse nor better) 26 to 50 Failure of the therapy 4 Somewhat improved 51 to 75 Successful therapy 5 Significantly improved 76 to 100 Successful therapy Inclusion criteria This study included patients with moderate to severe interstitial cystitis who had participated in the experimental trial conducted in January 2023 at the UroGyn Specialists of Florida clinic using the nonFDA-approved BPC-157 peptide

Bohler F, Bohler L, Taranikanti V