Cingulate (CING) Registration filing summary
Event summary combining transcript, slides, and related documents.
Registration filing summary
20 Mar, 2026Company overview and business model
Biopharmaceutical company leveraging proprietary Precision Timed Release (PTR) technology to develop next-generation pharmaceuticals targeting conditions with burdensome dosing and suboptimal outcomes, initially focusing on ADHD and anxiety.
Pipeline includes CTx-1301 (dexmethylphenidate) and CTx-1302 (dextroamphetamine) for ADHD, and CTx-2103 (buspirone) for anxiety, aiming to provide true once-daily dosing and improved patient outcomes.
PTR platform uses a proprietary Erosion Barrier Layer to enable controlled, multi-dose release in a single tablet.
Financial performance and metrics
As of March 13, 2026, 11,594,679 shares of common stock were outstanding; up to 3,500,000 additional shares may be issued in this offering.
The company qualifies as an emerging growth company with less than $1.235 billion in annual revenue and benefits from reduced reporting requirements.
Audit report notes substantial doubt about the company's ability to continue as a going concern due to losses and negative cash flows.
Use of proceeds and capital allocation
Proceeds from sales to Lincoln Park will be used for regulatory approval, development, manufacturing, and commercialization of CTx-1301, as well as working capital, capital expenditures, and general corporate purposes, including further R&D.
Management has broad discretion over the use of proceeds, which may also be invested in complementary businesses or technologies.
Latest events from Cingulate
- Shareholders will vote on director election, auditor ratification, and expanding the equity incentive plan.CING
Proxy filing29 May 2026 - Key votes include director election, auditor ratification, and expanding the equity plan.CING
Proxy filing29 May 2026 - Board recommends approval of director election, auditor ratification, and equity plan amendment.CING
Proxy filing19 May 2026 - Q1 2026 net loss rose to $9.3M as cash climbed to $25.9M ahead of FDA review.CING
Q1 202614 May 2026 - CTX-1301 aims to disrupt the ADHD market with once-daily efficacy and strong clinical results.CING
Corporate presentation14 Apr 2026 - Advancing once-daily ADHD and anxiety drugs with $12M raised, but faces going concern risk.CING
Registration filing14 Apr 2026 - Shelf registration enables flexible securities issuance; auditor consent updated.CING
Registration filing23 Mar 2026 - Beneficial ownership table updated to include a 5% stockholder and clarify voting procedures.CING
Proxy Filing18 Mar 2026 - 2025 net loss widened to $22.4M as CTx-1301 advanced toward FDA review and $12M was raised.CING
Q4 202518 Mar 2026