Cingulate Initiates Final Study for Lead ADHD Asset CTx-1301
Cingulate Inc. (CING)
Company Research
Source: GlobeNewswire
KANSAS CITY, Kan., Sept. 12, 2024 (GLOBE NEWSWIRE) -- Cingulate Inc. (NASDAQ: CING), a biopharmaceutical company utilizing its proprietary Precision Timed Release™ (PTR™) drug delivery platform technology to build and advance a pipeline of next-generation pharmaceutical products, announced today that it has commenced its final FDA-required study, which is a food effect study, for CTx-1301 (dexmethylphenidate) for the treatment of Attention Deficit Hyperactivity Disorder (ADHD). A data readout from the study is expected by the end of 2024. Additionally, Cingulate has raised over $10 million in additional capital since the middle of August 2024, 58% of this amount from its at the market facility, and has received notification from Nasdaq that Cingulate is now in compliance with Nasdaq listing requirements. “We are pleased to have raised additional substantial capital, which allows us to focus on advancing the final activities required for NDA submission of our lead asset, CTx-13
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CING
News
- Cingulate to Participate in Benzinga All Live Access EventGlobeNewswire
- Cingulate Announces Adjournment of Special MeetingGlobeNewswire
- Cingulate Reports Second Quarter 2024 Financial Results and Provides Development Update on Major Milestones AchievedGlobeNewswire
- Collegium buys Ironshore for $525m and enter ADHD market [Yahoo! Finance]Yahoo! Finance
CING
Sec Filings
- 9/27/24 - Form S-1
- 9/12/24 - Form 8-K
- 9/10/24 - Form 8-K
- CING's page on the SEC website