Cingulate Inc. is a biopharmaceutical enterprise currently in its clinical development phase, dedicated to devising therapeutic options for attention-deficit/hyperactivity disorder (ADHD). Leading its pipeline for ADHD are two drug candidates: CTx-1301 (dexmethylphenidate), which is currently progressing through Phase 3 clinical trials, and CTx-1302 (dextroamphetamine). The company is also engaged in the advancement of CTx-2103, a candidate intended for the management of anxiety disorders. Founded in 2012, Cingulate Inc. maintains its corporate headquarters in Kansas City, Kansas.
Cingulate Inc. Reports Second Quarter 2026 Financial Results and Provides Update on CTx-1301 CMC Progress Towards NDA Resubmission and Commercial Readiness
Cingulate reported second quarter 2026 financial results, ending the period with $28.4 million in cash and cash equivalents, extending its operational runway into mid-2027.
The company is progressing on CMC work to support the resubmission of the NDA for CTx-1301 following a Complete Response Letter, while securing a new U.S. patent covering the asset through December 2042.
Commercialization preparations advanced with the signing of agreements with Prasco for distribution and Indegene for commercial operations, although SG&A expenses doubled to $3.9 million to support this build-out.