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The Week in Review: May 20-24

The Week in Review: May 20-24
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FDA Clears Cingulate to File NDA for CTx-1301 in the Treatment of ADHD

The company has announced plans to submit the NDA in the first half of 2025.

United statesAnn childressShanej schafferAmerican professional societyDrug administrationBehavior medicine incCingulate incNew drug applicationRelated disordersAnnual meetingPermanent product measure

FDA Clears Cingulate to File for Marketing Approval of

Phase 3 Data Collected to Date Sufficient for Submission of New Drug Application Advancing Discussions with Commercialization Partners.

United statesKansas cityShanej schafferMatt krepsThomas daltonAnn childressDarrow associatesExchange commissionPsych congress first annual posterDrug administrationAmerican professional societyBehavior medicine incSecurities exchangePsych congressPlatform technologyCingulate inc

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

Phase 3 Data Collected to Date Sufficient for Submission of New Drug Application CTx-1301 Could Benefit >60% of ADHD Patients Currently .

United statesKansas cityShanej schafferMatt krepsThomas daltonAnn childressDrug administrationBehavior medicine incPlatform technologySecurities exchangeDarrow associatesPsych congress first annual posterExchange commissionPsych congressCingulate incAmerican professional society

Peter J Werth, Successful Pharma Entrepreneur, Philanthropist, Cingulate Investor and Board

KANSAS CITY, Kan., April 30, 2024 (GLOBE NEWSWIRE) Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform technology to build and

United statesKansas cityThomas daltonShanej schafferPeterj werthMatt krepsBenzinga youtubeSecurities exchangeExchange commissionChemwerth incCingulate incDarrow associatesPrecision timed releaseCingulate chairmanBenzinga all accessFriday may

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