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FDA Clears Cingulate to File NDA for CTx-1301 in the Treatment of ADHD - Vimarsana News

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.

FDA Clears Cingulate to File for Marketing Approval of - Vimarsana News

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...

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

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 ...

Peter J. Werth, Successful Pharma Entrepreneur, Philanthropist, Cingulate Investor and Board ... - Vimarsana News

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

Peter J. Werth, Successful Pharma Entrepreneur, Philanthropist, Cingulate Investor and Board Member, to be Featured with Chairman and CEO Shane J. Schaffer on Benzinga All Live Access - Vimarsana News

Peter J. Werth, Successful Pharma Entrepreneur, Philanthropist, Cingulate Investor and Board Member, to be Featured with Chairman and CEO Shane J. Schaffer on Benzinga All Live Access

KANSAS CITY, Kan., April 30, 2024 -- Cingulate Inc. , a biopharmaceutical company utilizing its proprietary Precision Timed Release™ drug delivery platform technology to build and advance a...