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The FDA also cited the company for using unvalidated laboratory testing methods that failed to detect impurities and for inadequate equipment cleaning and cleaning validation practices that increased the risk of cross-contamination between products

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With a small sample size of just 36 total participants, the trial had involved treating 20 COVID-19 patients with 600 milligrams of hydroxychloroquine, a drug best known as an antimalarial

Week 24+ Maximum clinical efficacy

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