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Each production lot undergoes chromatographic purity analysis, molecular identity confirmation, and rigorous quality review before release, ensuring consistent quality for scientific research and laboratory procurement

The cardiovascular outcomes trial reported in the same label randomised 8,801 and 8,803 participants and found a primary composite endpoint of 6.5% versus 8% with placebo, hazard ratio 0.80 (95% CI 0.72 to 0.90)

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