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They are not intended to represent clinical evidence in humans, and BPC+TB Blend has not been approved by the FDA, EMA, or any other regulatory authority for any indication
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By inhibiting drug-metabolizing enzymes (e.g., cytochrome P450, UDP-glucuronosyltransferase) and enhancing intestinal absorption (21, 32), PPR significantly inhibits P-glycoprotein (P-gp) and enhances the efficacy of co-administered compounds like CUR and RSV, positioning it as a critical adjunct in nutraceutical formulations (33, 34)
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