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Clinical Research Findings on AOD-9604 In clinical trials involving approximately 900 participants across six human studies, AOD-9604 demonstrated a favorable safety and tolerability profile

The FDA issued a warning letter to an Indian API manufacturer after inspectors found that the company knowingly accepted deliberately mislabeled raw materials to bypass licensing requirements, failed to perform required identity testing, and relied on unverified supplier documentation before using the materials to manufacture APIs shipped to the United States

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