Cingulate's ADHD Drug CTx-1301 Receives Patent Allowance
On Tuesday, March 17th, 2026, the United States Patent and Trademark Office issued a Notice of Allowance for a patent application covering Cingulate's lead ADHD candidate, CTx-1301, indicating that the agency has completed its examination and determined that the claims are allowable. Upon issuance, the patent is expected to provide protection through May 2042 for key aspects of CTx-1301's formulation and method of use, further strengthening Cingulate's intellectual property portfolio surrounding its Precision Timed Release platform, which is designed to enable the development of next-generation therapeutics with customized release profiles.
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- Financial Performance: Cingulate reported a net loss of $6.3 million for Q4 2025, slightly up from $6.2 million in Q4 2024, indicating ongoing challenges in achieving profitability.
- Cash Flow Status: As of December 31, 2025, Cingulate had approximately $11.0 million in cash and cash equivalents, a decrease of $1.3 million from the previous year, reflecting pressure on the company's liquidity management.
- Working Capital Changes: The reduction in working capital may impact the company's future investment capabilities and operational flexibility, particularly in research and development and marketing efforts.
- Market Reaction: Despite the lack of significant improvement in financial data, investors remain cautiously optimistic about Cingulate's long-term potential, which may influence its stock price performance.
- Patent Approval: The USPTO has approved Cingulate's ADHD drug patent application filed in November 2023, marking a significant advancement in the company's neurological treatment technologies and expected to provide crucial support for an upcoming regulatory decision.
- Technological Innovation: The patent covers the 'Trimodal, Precision-Timed Pulsatile Release Tablet' technology, which releases medication at multiple timed intervals throughout the day, aiming to address common issues with stimulant medications, thereby enhancing patient experience.
- Positive Market Reaction: Following the patent approval, Cingulate's shares jumped over 4% in pre-market trading on Sunday, reflecting investor optimism about the company's future, especially in light of the impending FDA decision.
- Successful Clinical Trials: Before submitting the New Drug Application, Cingulate completed Phase 3 trials in both adult and pediatric patients, demonstrating significant improvements in ADHD symptoms, which further bolsters market confidence in its product.
- Coherus Performance: Coherus Oncology, Inc. (CHRS) rose 9.09% in after-hours trading, closing at $1.73 with a $0.14 gain, indicating strong investor confidence in its future prospects.
- Sensei Biotech Surge: Sensei Biotherapeutics, Inc. (SNSE) surged 10.06% after hours, finishing at $12.47 with a $1.14 increase, reflecting positive market expectations for its products.
- uniQure Significant Jump: uniQure N.V. (QURE) posted a 9.96% rise in after-hours trading, closing at $24.95 with a $2.26 gain, suggesting investor optimism regarding its R&D progress.
- IO Biotech Strategic Exploration: Although IO Biotech, Inc. (IOBT) had no fresh news on Thursday, its stock still gained 4.19%, closing at $0.50, indicating market interest in its exploration of strategic alternatives, including potential mergers or asset sales.
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Femasys Gains: Femasys Inc. (FEMY) saw an 18% increase following the launch of a post-market clinical study for its FemBloc Permanent Birth Control, complying with EU regulations.
Cingulate's Presentation: Cingulate Inc. (CING) rose over 6% after announcing that data from its ADHD treatment candidate, CTx-1301, will be presented at the AACAP Annual Meeting, highlighting its potential in ADHD management.
Community Health Systems Performance: Community Health Systems, Inc. (CYH) shares increased over 4% after reporting positive Q3 results, contributing to a generally favorable after-hours trading environment for biotech stocks.

CTx-1301 Presentation: Cingulate Inc. announced that data from its ADHD candidate CTx-1301 will be presented at the AACAP Annual Meeting, highlighting its once-daily, extended-release formulation aimed at improving treatment for ADHD patients.
Expert Presentation: Dr. Ann Childress, a leading ADHD specialist, will present the Phase 3 trial results, emphasizing CTx-1301's efficacy and safety in pediatric subjects with ADHD.
Innovative Drug Delivery: CTx-1301 utilizes Cingulate's Precision Timed Release™ platform to provide three timed releases of medication throughout the day, addressing limitations of current stimulant therapies.
Company Overview: Cingulate Inc. is focused on developing next-generation pharmaceutical products to enhance patient outcomes, with CTx-1301 in late-stage development for ADHD and other candidates targeting anxiety and neuropsychiatric conditions.







