Cingulate Completes First Cohort of Phase 3 Adult Onset and Duration Trial of CTx-1301 (dexmethylphenidate) for ADHD
Trial On Track for 3Q 2023 Results
Pivotal Phase 3 Trial in Pediatric/Adolescent Patients Planned to Begin Mid-2023
KANSAS CITY, Kan., April 04, 2023 (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, today announced it has completed the first cohort of its Phase 3 adult onset and duration trial of its lead candidate, CTx-1301 (dexmethylphenidate), for attention deficit/hyperactivity disorder (ADHD).
Related news for (CING)
- Stonegate Capital Partners Initiates Coverage on Cingulate Inc. (CING)
- 24/7 Market News Snapshot 20 May, 2025 – Cingulate Inc. Common Stock (NASDAQ:CING)
- Efficacy Results Announced from Cingulate’s Phase 3 Pediatric Study of CTx-1301 (dexmethylphenidate) for ADHD
- FDA and Cingulate Aligned with Filing Requirements for New Drug Application for Lead ADHD Asset CTx-1301
- 24/7 Market News Snapshot 14 May, 2025 – Cingulate Inc. Common Stock (NASDAQ:CING)