Cingulate Inc. Advances Towards FDA Approval for CTx-1301

Story Highlights
  • Cingulate announced safety results for CTx-1301, showing no serious adverse events.
  • Results submitted to FDA, aiming for mid-2025 approval, enhancing ADHD treatment options.
  • Looking for the best stocks to buy? Follow the recommendations of top-performing analysts.
Cingulate Inc. Advances Towards FDA Approval for CTx-1301

An update from Cingulate Inc ( (CING) ) is now available.

On March 4, 2025, Cingulate Inc. announced the safety results from its final Phase 3 trials for CTx-1301, a novel, once-daily stimulant medication for ADHD, which showed no serious adverse events and consistent safety profiles. The results, submitted to the FDA ahead of an April 2 meeting, mark a significant step towards filing for FDA approval mid-2025, potentially positioning Cingulate as a leader in ADHD treatment with a product that addresses unmet needs in the market.

More about Cingulate Inc

Cingulate Inc. is a biopharmaceutical company that utilizes its proprietary Precision Timed Release (PTR) drug delivery platform technology to develop next-generation pharmaceutical products. The company focuses on improving the lives of patients with conditions that require burdensome daily dosing regimens, with an initial emphasis on treating Attention Deficit Hyperactivity Disorder (ADHD).

YTD Price Performance: -19.22%

Average Trading Volume: 141,111

Technical Sentiment Consensus Rating: Buy

Current Market Cap: $13.23M

Learn more about CING stock on TipRanks’ Stock Analysis page.

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