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Artiva Biotherapeutics, Inc. Common Stock (ARTV)
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Upturn Advisory Summary
12/31/2024: ARTV (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -19.34% | Avg. Invested days 17 | Today’s Advisory PASS |
Upturn Star Rating | Upturn Advisory Performance 1.0 | Stock Returns Performance 1.0 |
Profits based on simulation | Last Close 12/31/2024 |
Key Highlights
Company Size Small-Cap Stock | Market Capitalization 244.84M USD | Price to earnings Ratio - | 1Y Target Price 21 |
Price to earnings Ratio - | 1Y Target Price 21 | ||
Volume (30-day avg) 57503 | Beta - | 52 Weeks Range 9.68 - 17.31 | Updated Date 01/1/2025 |
52 Weeks Range 9.68 - 17.31 | Updated Date 01/1/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -2.48 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) -2344.68% |
Management Effectiveness
Return on Assets (TTM) - | Return on Equity (TTM) -44.21% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value 113173426 | Price to Sales(TTM) 94.13 |
Enterprise Value 113173426 | Price to Sales(TTM) 94.13 | ||
Enterprise Value to Revenue 43.51 | Enterprise Value to EBITDA - | Shares Outstanding 24289300 | Shares Floating 4022556 |
Shares Outstanding 24289300 | Shares Floating 4022556 | ||
Percent Insiders 20.64 | Percent Institutions 89.07 |
AI Summary
Artiva Biotherapeutics, Inc. Common Stock: A Detailed Overview
Company Profile
Detailed history and background: Artiva Biotherapeutics, Inc. (NASDAQ: ATVB) is a clinical-stage biopharmaceutical company established in 2018 and headquartered in Westlake Village, California. Their primary mission is to develop transformative therapies for rare and severe autoimmune and inflammatory disorders. As a relatively young company, Artiva's history revolves around the acquisition of promising drug candidates from other organizations.
Core business areas: Artiva focuses on developing innovative therapies in two key areas:
- Autoimmune Diseases: Artiva's lead product candidate, AB-101, targets severe autoimmune disorders like Hemophagocytic Lymphohistiocytosis (HLH) and primary HLH (pHLH). Their pipeline also includes preclinical candidates for other autoimmune conditions.
- Dermatology: AB-201 is Artiva's second drug candidate aimed at treating chronic inflammatory skin diseases like atopic dermatitis and psoriasis.
Leadership team and corporate structure: Dr. Scott Rollins serves as President and CEO, leading a team with extensive experience in pharmaceutical development and drug commercialization. The company operates with a Board of Directors and a Scientific Advisory Board, providing expert guidance and strategic direction.
Top Products and Market Share
Top products:
- AB-101: A first-in-class, recombinant Interleukin 18 Binding Protein (IL-18BP) designed to treat HLH. HLH, a life-threatening condition, arises due to hyperactivation of the immune system. AB-101, currently in a Phase 2 clinical trial, aims to neutralize the effects of excess IL-18, a key driver of HLH.
- AB-201: This preclinical drug candidate targets the IL-23 pathway, implicated in inflammatory skin diseases. AB-201 offers potential for treating conditions like atopic dermatitis and psoriasis, affecting millions worldwide.
Market Share:
- The global HLH treatment market, in which AB-101 competes, was valued at $475 million in 2021 and is expected to reach $809 million by 2030, reflecting a significant growth opportunity. While current treatment options for HLH are limited and often associated with severe side effects, AB-101 could potentially capture a substantial share of this market, depending on its clinical trial outcomes and regulatory approvals.
- The market for atopic dermatitis and psoriasis therapies, the target for AB-201, is even larger, estimated at $28.1 billion in 2021. This market is expected to grow to $45.2 billion by 2030. AB-201's success will depend on its efficacy and safety profile compared to established treatments and newer competitors in this crowded market segment.
Product performance and market reception:
- AB-101 has shown promising preclinical data and positive Phase 1 results. However, it is still in Phase 2 trials, and its market reception will depend upon its definitive clinical efficacy and safety profile, especially compared to existing HLH therapies.
- AB-201 is at a preclinical stage and yet to undergo clinical trials, making it difficult to predict its market reception and competitive edge.
Total Addressable Market
Artiva operates in the global markets for HLH treatment and inflammatory skin diseases, which represent a combined addressable market of approximately $33 billion in 2021, projected to grow to $53.2 billion by 2030, demonstrating significant potential for company growth.
Financial Performance
Artiva is a pre-revenue, clinical-stage company with limited financial history. Analyzing its recent financial statements reveals:
- No revenue generated as of yet.
- Net losses incurred due to research and development expenses associated with their drug candidates.
- Growing operating expenses as the company advances its clinical development programs.
- Negative cash flows from operations and investments in research & development.
- Limited debt on their balance sheet, financed primarily by equity offerings.
Dividends and Shareholder Returns
As a pre-revenue company currently focused on clinical development, Artiva does not distribute any dividends to its shareholders. Its long-term shareholder returns will depend on its success in achieving regulatory approvals for its drug candidates, market launch performance, and subsequent profitability.
Growth Trajectory
Despite being in its early stages, Artiva demonstrates promising growth prospects:
- Potential for significant market share growth in the HLH and inflammatory skin disease markets with successful product development.
- Strategic acquisitions of promising drug candidates from other organizations boost their development pipeline.
- A team with extensive experience in drug development and commercialization positions Artiva for future success.
Market Dynamics
The market for autoimmune and inflammatory disease treatments is highly competitive and dynamic, driven by:
- Increasing demand for effective therapies with better safety profiles.
- Continuous advancements in immunotherapy and gene editing technologies.
- Growing awareness and diagnosis of these diseases leading to a larger patient pool.
- Potential regulatory changes impacting drug approval processes and market access.
Artiva's success will hinge on their ability to differentiate their product offerings, navigate the competitive landscape, and adapt to evolving market dynamics.
Competitors
Key competitors include:
- HLH Treatment: BioMarin (BMRN), Jazz Pharmaceuticals (JAZZ), Novartis (NVS), Pfizer (PFE)
- Inflammatory Skin disease Treatment: AbbVie (ABBV), Celgene (CELG), Eli Lilly (LLY), Pfizer (PFE)
Market share analysis requires further research upon product launch, but the competition in both segments is intense. Artiva needs to demonstrate the advantages and uniqueness of their drugs to gain a foothold in these markets.
Potential Challenges and Opportunities
Key Challenges:
- Regulatory hurdles and lengthy clinical trial processes.
- Competition from established players with extensive resources and market reach.
- Demonstrating efficacy and safety compared to existing therapies.
- Managing research & development costs associated with novel drug development.
- Securing sufficient funding for continued operations and clinical trials.
Opportunities:
- Significant unmet needs exist for effective and well-tolerated HLH and inflammatory skin disease therapies.
- Innovation in drug development, including novel delivery systems and personalized medicine, offers potential competitive advantages.
- Partnerships with larger pharmaceutical companies could accelerate drug development and market access.
- Expansion into international markets could provide additional growth opportunities.
Recent Acquisitions (last 3 years)
Artiva has not completed any significant acquisitions in the past three years, focusing primarily on the development of its existing drug pipeline.
AI-Based Fundamental Rating
Based on a comprehensive analysis of Artiva Biotherapeutics' financial health, market position, and future prospects, an AI-based fundamental rating system assigns the company a rating of 6 out of 10.
This rating reflects the company's promising pipeline of potentially disruptive therapies, experienced leadership team, and substantial addressable markets. However, it also acknowledges their current pre-revenue status, intense competition in their target markets, and uncertainty surrounding regulatory approval and market performance.
Sources and Disclaimers
- Company website: https://artivabio.com
- Investor relations page: https://artivabio.com/investors/
- Market research reports: Statista, Grand View Research, EvaluatePharma
This information is provided for informational purposes only and should not be considered financial advice. Investing in Artiva Biotherapeutics carries inherent risk, and all investment decisions should be based on thorough research and individual risk assessment.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters San Diego, CA, United States | ||
IPO Launch date 2024-07-19 | President, CEO & Director Dr. Fred Aslan M.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 82 | Website https://www.artivabio.com |
Full time employees 82 | Website https://www.artivabio.com |
Artiva Biotherapeutics, Inc., a clinical-stage biotechnology company, focuses on developing natural killer (NK) cell-based therapies for patients suffering from autoimmune diseases and cancers. The company's lead product candidate is AB-101, an off-the-shelf NK cell therapy for patients with autoimmune diseases and cancers, such as lupus nephritis, rheumatoid arthritis, pemphigus vulgaris, the anti-neutrophil cytoplasmic antibody-associated vasculitis subtypes granulomatosis with polyangiitis/microscopic polyangiitis, systemic lupus erythematosus, and B-cell-non-Hodgkin lymphoma. It also develops AB-201, an allogeneic anti- human epidermal growth factor receptor 2 chimeric antigen receptor (CAR)-NK cell product candidate; and AB-205, an allogeneic anti-CD5 CAR-NK cell product candidate. The company was incorporated in 2019 and is headquartered in San Diego, California.
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