Sydnexis is a verifiable clinical-stage biopharmaceutical company (Series B, ~$76.5M funding) focused on pediatric myopia. While the entity has significant capital and has achieved EU marketing approval (Ryjunea), the project submission contains low-quality, exaggerated claims (e.g., 'most people have used my product', 'audience: everyone') which contradict the specialized medical nature of the product. Additionally, a recent FDA Complete Response Letter (Oct 2025) presents a significant regulatory hurdle in the US market.
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