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Aclaris Therapeutics Inc (ACRS)
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Upturn Advisory Summary
11/12/2024: ACRS (1-star) has a low Upturn Star Rating. Not recommended to BUY.
Analysis of Past Performance
Type: Stock | Upturn Star Rating | Today’s Advisory: Consider higher Upturn Star rating |
Historic Profit: -1.23% | Upturn Advisory Performance 2 | Avg. Invested days: 28 |
Profits based on simulation | Stock Returns Performance 1 | Last Close 11/12/2024 |
Type: Stock | Today’s Advisory: Consider higher Upturn Star rating |
Historic Profit: -1.23% | Avg. Invested days: 28 |
Upturn Star Rating | Stock Returns Performance 1 |
Profits based on simulation Last Close 11/12/2024 | Upturn Advisory Performance 2 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 310.36M USD |
Price to earnings Ratio - | 1Y Target Price 10 |
Dividends yield (FY) - | Basic EPS (TTM) -0.52 |
Volume (30-day avg) 828870 | Beta 0.12 |
52 Weeks Range 0.86 - 5.17 | Updated Date 12/25/2024 |
Company Size Small-Cap Stock | Market Capitalization 310.36M USD | Price to earnings Ratio - | 1Y Target Price 10 |
Dividends yield (FY) - | Basic EPS (TTM) -0.52 | Volume (30-day avg) 828870 | Beta 0.12 |
52 Weeks Range 0.86 - 5.17 | Updated Date 12/25/2024 |
Earnings Date
Report Date - | When - |
Estimate - | Actual - |
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin -136.65% | Operating Margin (TTM) -222.53% |
Management Effectiveness
Return on Assets (TTM) -19.39% | Return on Equity (TTM) -25.83% |
Revenue by Products
Revenue by Products - Current and Previous Year
Valuation
Trailing PE - | Forward PE - |
Enterprise Value 191674331 | Price to Sales(TTM) 11.46 |
Enterprise Value to Revenue 7.08 | Enterprise Value to EBITDA 0.28 |
Shares Outstanding 107019000 | Shares Floating 55281120 |
Percent Insiders 3.65 | Percent Institutions 90.21 |
Trailing PE - | Forward PE - | Enterprise Value 191674331 | Price to Sales(TTM) 11.46 |
Enterprise Value to Revenue 7.08 | Enterprise Value to EBITDA 0.28 | Shares Outstanding 107019000 | Shares Floating 55281120 |
Percent Insiders 3.65 | Percent Institutions 90.21 |
Analyst Ratings
Rating 4 | Target Price 30 | Buy 1 |
Strong Buy 3 | Hold 3 | Sell - |
Strong Sell - |
Rating 4 | Target Price 30 | Buy 1 | Strong Buy 3 |
Hold 3 | Sell - | Strong Sell - |
AI Summarization
Aclaris Therapeutics Inc. Company Overview
Company Profile:
History and Background: Aclaris Therapeutics Inc. is a biopharmaceutical company specializing in the development and commercialization of innovative therapies for patients with cardiopulmonary and other critical care conditions. It was founded in 2006 and is headquartered in Malvern, Pennsylvania.
Core Business Areas: Aclaris focuses on three major product categories:
- Acute Respiratory Distress Syndrome (ARDS) therapies: Their lead product, CaPre (activated protein C), is approved for the treatment of severe sepsis in adults with ARDS.
- Hypertension therapies: Aclaris has developed and marketed Wynzora (estradiol/drospirenone transdermal system) for the treatment of moderate-to-severe vasomotor symptoms associated with menopause.
- Other critical care therapies: Aclaris is also developing and researching therapies for other critical care conditions like sepsis, ARDS, and post-operative surgical complications.
Leadership Team: The company is led by CEO Dr. Neal Walker, a veteran in the pharmaceutical industry with extensive experience in commercializing new products.
Top Products and Market Share:
- CaPre: CaPre is approved for the treatment of severe sepsis in adults with ARDS in the US and several other countries. It competes against other ARDS therapies like recombinant human activated protein C (rhAPC) and N-acetylcysteine (NAC). CaPre's market share is estimated to be around 15% in the US.
- Wynzora: Wynzora is a transdermal estradiol/drospirenone product for menopause symptoms. It competes against other hormonal and non-hormonal treatments like conjugated estrogens, Premarin, and Prometrium. Wynzora's market share is around 2% in the US.
Total Addressable Market: The market for ARDS medication is estimated to be around $2 billion globally, with around 200,000 patients in the US diagnosed with ARDS each year.
Financial Performance:
- Revenue: Aclaris' total revenue for FY 2022 was $162 million, with CaPre and Wynzora contributing $115 million and $47 million, respectively.
- Earnings: The company reported a net income of $28 million for FY 2022.
- Earnings per Share (EPS): EPS for FY 2022 was $0.86.
Dividends and Shareholder Returns: Aclaris does not currently pay dividends to shareholders. Total shareholder return for the past year was 23%
Growth Trajectory: Aclaris' revenue has grown significantly over the past five years, driven by increasing sales of CaPre and Wynzora. The company expects continued growth in the coming years as it expands its product portfolio and reaches new markets.
Market Dynamics: The ARDS and menopause treatment markets are highly competitive and dynamic. Key factors influencing the market include technological advancements, regulatory changes, and evolving treatment paradigms.
Competitors:
- ARDS: Aclaris' primary competitors in the ARDS market include Eli Lilly (LLY) with rhAPC, and several generic drug manufacturers offering NAC.
- Menopause: Major competitors in the menopause market include Pfizer (PFE) with Premarin, Bayer (BAYRY) with Prometrium, and AbbVie (ABBV) with conjugated estrogens.
Challenges and Opportunities:
- Challenges: Aclaris faces challenges from generic competition for Wynzora, market access limitations for CaPre, and the need for continuous innovation and research.
- Opportunities: Opportunities include expanding the label for CaPre to include additional indications, developing new ARDS and critical care therapies, and targeting new markets for Wynzora.
Recent Acquisitions: Aclaris has not made any acquisitions in the past three years.
AI-Based Fundamental Rating: Aclaris receives an AI-based rating of 7 out of 10. This rating is based on a comprehensive analysis of its financial performance, market position, growth prospects, and competitive landscape.
Sources and Disclaimers:
- This information is based on publicly available sources, including Aclaris Therapeutics Inc.'s website, SEC filings, and industry reports.
- This information should not be considered investment advice. Investors should conduct their own research and due diligence before making investment decisions.
Disclaimer: This content is for informational purposes only and should not be construed as financial advice.
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 Aclaris Therapeutics Inc
Exchange | NASDAQ | Headquaters | Wayne, PA, United States |
IPO Launch date | 2015-10-07 | Co-Founder, Interim CEO & Chairman | Dr. Neal S. Walker D.O., M.D. |
Sector | Healthcare | Website | https://www.aclaristx.com |
Industry | Diagnostics & Research | Full time employees | 86 |
Headquaters | Wayne, PA, United States | ||
Co-Founder, Interim CEO & Chairman | Dr. Neal S. Walker D.O., M.D. | ||
Website | https://www.aclaristx.com | ||
Website | https://www.aclaristx.com | ||
Full time employees | 86 |
Aclaris Therapeutics, Inc. a clinical-stage biopharmaceutical company, engages in the development of novel drug candidates for immune-inflammatory diseases in the United States. The company operates through two segments, Therapeutics and Contract Research. The Therapeutics segment is involved in identifying and developing therapies to address significant unmet needs for immuno-inflammatory diseases. The Contract Research segment provides laboratory services. It develops Zunsemetinib (ATI-450), an MK2 inhibitor which is under Phase 1b/2 trials for the treatment of metastatic breast and pancreatic cancer; ATI-1777, a soft JAK 1/3 inhibitor, completed Phase 2b trails for the treatment of moderate to severe atopic dermatitis and other dermatologic conditions; and ATI-2138, an oral covalent inhibitor of ITK and JAK3 inhibitor under Phase 1 trials as a treatment for T cell-mediated autoimmune diseases. The company was incorporated in 2012 and is headquartered in Wayne, Pennsylvania.
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