FDA
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Cingulate reports positive phase 3 trial results for ADHD drug CTx-1301
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Stonegate Capital Partners Updates Coverage on Cingulate Inc. (CING) 2Q25
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Cingulate Receives $4.3M Waiver from FDA Ahead of Imminent Filing for Marketing Approval of Lead ADHD Asset CTx-1301
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FDA and Cingulate Aligned with Filing Requirements for New Drug Application for Lead ADHD Asset CTx-1301
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Cingulate Reports Safety Results from Final Phase 3 Trials for Lead ADHD Asset CTx-1301: On Track to File for FDA Approval Mid-2025
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Cingulate Issued European Patent for Lead Asset CTx-1301 for the Treatment of ADHD
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Cingulate to Attend DCAT Week 2024 in New York City
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