Cingulate Cleared by FDA to File for Marketing Approval of CTx-1301 in the Treatment of ADHD

DENVER, Colo., May 21, 2024 (247marketnews.com)- Cingulate Inc. (NASDAQ:CING) received confirmation from the U.S. Food and Drug Administration (FDA) on the requirements necessary for filing a New Drug Application (NDA), which the Company expects to submit in the first half of 2025, for its lead Phase 3 candidate CTx-1301 (dexmethylphenidate), for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in patients six years of age or older.

“We are pleased with the FDA’s guidance and perspective regarding our pathway to a timely NDA filing, and we will proceed to complete all remaining requirements accordingly,” commented Shane Schaffer, Cingulate’s Chairman and CEO. “We also believe this communication provides additional go-to-market momentum as we continue to meet with potential partners for the outlicensing of CTx-1301 in the United States and abroad. Now that we have a clear path to submission, we look forward to engaging with key payer stakeholders to achieve maximum access and market penetration to benefit ADHD patients and their families.”

“The treatment effect size of CTx-1301 was remarkable given the current effect sizes observed in the marketplace. Many patients require longer duration of efficacy and must add a second, or booster, dose to ensure treatment effect over their entire active day. The patients I observed, once notified they were taking CTx-1301, have expressed a desire to remain on the medication after the trial concluded,” stated Ann Childress, M.D., President, Center for Psychiatry and Behavior Medicine, Inc.

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