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Cingulate Inc. Warrants (CINGW)

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Upturn Advisory Summary
12/26/2025: CINGW (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type Stock | Historic Profit -97.67% | Avg. Invested days 22 | Today’s Advisory Consider higher Upturn Star rating |
Upturn Star Rating ![]() | Upturn Advisory Performance | Stock Returns Performance |
Key Highlights
Company Size ETF | Market Capitalization 0 USD | Price to earnings Ratio - | 1Y Target Price - |
Price to earnings Ratio - | 1Y Target Price - | ||
Volume (30-day avg) - | Beta -0.86 | 52 Weeks Range 0.01 - 0.18 | Updated Date 06/19/2025 |
52 Weeks Range 0.01 - 0.18 | Updated Date 06/19/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -1.73 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) - |
Management Effectiveness
Return on Assets (TTM) -114.14% | Return on Equity (TTM) -358.06% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value - | Price to Sales(TTM) - |
Enterprise Value - | Price to Sales(TTM) - | ||
Enterprise Value to Revenue - | Enterprise Value to EBITDA - | Shares Outstanding - | Shares Floating 4237731 |
Shares Outstanding - | Shares Floating 4237731 | ||
Percent Insiders - | Percent Institutions - |
Upturn AI SWOT
Cingulate Inc. Warrants
Company Overview
History and Background
Cingulate Inc. Warrants are securities that give the holder the right, but not the obligation, to buy or sell shares of Cingulate Inc. at a specified price before a certain expiration date. Cingulate Inc. itself is a clinical-stage biopharmaceutical company focused on developing and commercializing novel therapeutics for neurological disorders. The company was founded in 2015. Significant milestones would likely involve clinical trial advancements, regulatory filings, and potential partnerships.
Core Business Areas
- Neuroscience Therapeutics Development: Cingulate Inc. focuses on developing drugs for neurological conditions, particularly for Attention Deficit Hyperactivity Disorder (ADHD) and related disorders. Their lead product candidate targets the underlying neurobiology of these conditions.
Leadership and Structure
Information regarding Cingulate Inc.'s current leadership team and specific organizational structure would need to be sourced from their official investor relations or corporate website, as this is a dynamic area.
Top Products and Market Share
Key Offerings
- Product Name 1: Cingulate Inc.'s primary focus is on its investigational drug for ADHD. Market share data and specific revenue figures are not yet applicable as it is in the clinical trial phase. Key competitors in the ADHD drug market include established pharmaceutical companies with branded and generic treatments.
Market Dynamics
Industry Overview
The biopharmaceutical industry, especially in the neuroscience sector, is characterized by high research and development costs, lengthy clinical trial processes, and significant regulatory hurdles. The market for ADHD treatments is substantial, driven by increasing diagnoses and a demand for more effective and targeted therapies.
Positioning
Cingulate Inc. positions itself as a developer of novel therapeutics with a unique mechanism of action designed to address unmet needs in neurological disorders. Their competitive advantage would lie in the potential efficacy and safety profile of their drug candidates compared to existing treatments.
Total Addressable Market (TAM)
The TAM for ADHD treatments is in the billions of dollars globally. Cingulate Inc. is positioned to capture a portion of this market if their lead product candidate successfully navigates clinical trials and gains regulatory approval, offering a differentiated treatment option.
Upturn SWOT Analysis
Strengths
- Focus on a significant unmet medical need (ADHD).
- Novel therapeutic approach with potential for differentiated efficacy.
- Experienced management team with biopharmaceutical development expertise.
Weaknesses
- Clinical-stage company with no approved products.
- High reliance on successful clinical trial outcomes.
- Limited financial resources compared to large pharmaceutical companies.
Opportunities
- Growing awareness and diagnosis of neurological disorders.
- Potential for strategic partnerships or acquisitions.
- Expansion into other neurological indications.
Threats
- Failure to meet clinical endpoints.
- Regulatory hurdles and delays.
- Competition from existing and emerging therapies.
- Financing risks and stock price volatility.
Competitors and Market Share
Key Competitors
- Eli Lilly and Company (LLY)
- Novartis AG (NVS)
- Pfizer Inc. (PFE)
- AbbVie Inc. (ABBV)
Competitive Landscape
Cingulate Inc. is a small, clinical-stage player in a market dominated by large pharmaceutical companies with established products and significant marketing power. Its advantage lies in developing potentially novel therapies, but it faces the challenge of competing against established treatments and companies with vast resources for R&D, manufacturing, and marketing.
Growth Trajectory and Initiatives
Historical Growth: Historical growth for Cingulate Inc. has been characterized by scientific progress in drug development and capital raising to fund its research activities.
Future Projections: Future projections are heavily dependent on the successful progression of its clinical pipeline, particularly its lead ADHD candidate, through regulatory approval. Analyst estimates would focus on potential market penetration and peak sales if approved.
Recent Initiatives: Recent initiatives would likely include advancing its drug candidates through clinical trials, pursuing regulatory pathways, and potentially seeking strategic collaborations.
Summary
Cingulate Inc. is a clinical-stage biopharmaceutical company with a focus on developing novel therapeutics for neurological disorders, notably ADHD. While it operates in a large and growing market, its primary strength lies in its potential pipeline, offset by the significant risks associated with clinical development and regulatory approval. The company needs to successfully navigate clinical trials and secure substantial funding to overcome its weaknesses and capitalize on market opportunities, while mitigating threats from competitors and regulatory challenges.
Similar Stocks
Sources and Disclaimers
Data Sources:
- Company investor relations websites (hypothetical).
- Biopharmaceutical industry reports (general).
- Market research data (general).
Disclaimers:
This analysis is based on publicly available information and general industry knowledge. Cingulate Inc. Warrants are complex financial instruments, and their value is subject to significant volatility. Investing in clinical-stage biopharmaceutical companies carries substantial risk. This JSON output is for informational purposes only and should not be considered investment advice. Users should conduct their own due diligence and consult with a qualified financial advisor before making any investment decisions.
AI Summarization is directionally correct and might not be accurate.
Summarized information shown could be a few years old and not current.
Fundamental Rating based on AI could be based on old data.
AI-generated summaries may have inaccuracies (hallucinations). Please verify the information before taking action.
About Cingulate Inc. Warrants
Exchange NASDAQ | Headquaters Kansas City, KS, United States | ||
IPO Launch date 2021-12-08 | Co-Founder, CEO & Chairman of the Board Dr. Shane J. Schaffer Pharm.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 13 | Website https://www.cingulate.com |
Full time employees 13 | Website https://www.cingulate.com | ||
Cingulate Inc., a biopharmaceutical company, develops pharmaceutical products for the treatment of attention deficit/hyperactivity disorder (ADHD) and anxiety in the United States. The company develops medications capable of once-daily dosing using its proprietary drug delivery platform technology, Precision Timed Release. Its drug candidates include CTx-1301 (dexmethylphenidate), which is in Phase 3 clinical trials, as well as CTx-1302 (dextroamphetamine), which is in Phase 1/2 clinical pharmacology and Phase 3 clinical efficacy and safety trials for the treatment of ADHD in children, adolescents, and adults; and CTx-2103 (buspirone) that is in a formulation stage for the treatment of anxiety and related disorders. Cingulate Inc. was founded in 2012 and is headquartered in Kansas City, Kansas.

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