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Bioatla Inc (BCAB)
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Upturn Advisory Summary
12/31/2024: BCAB (1-star) is currently NOT-A-BUY. Pass it for now.
Analysis of Past Performance
Type Stock | Historic Profit -54.37% | Avg. Invested days 29 | 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 34.30M USD | Price to earnings Ratio - | 1Y Target Price 9 |
Price to earnings Ratio - | 1Y Target Price 9 | ||
Volume (30-day avg) 1068306 | Beta 1.02 | 52 Weeks Range 0.57 - 4.02 | Updated Date 01/1/2025 |
52 Weeks Range 0.57 - 4.02 | Updated Date 01/1/2025 | ||
Dividends yield (FY) - | Basic EPS (TTM) -1.7 |
Earnings Date
Report Date - | When - | Estimate - | Actual - |
Profitability
Profit Margin - | Operating Margin (TTM) -102.46% |
Management Effectiveness
Return on Assets (TTM) -50.47% | Return on Equity (TTM) -139.06% |
Valuation
Trailing PE - | Forward PE - | Enterprise Value -22281409 | Price to Sales(TTM) 3.12 |
Enterprise Value -22281409 | Price to Sales(TTM) 3.12 | ||
Enterprise Value to Revenue 2.25 | Enterprise Value to EBITDA 0.31 | Shares Outstanding 58024700 | Shares Floating 37475554 |
Shares Outstanding 58024700 | Shares Floating 37475554 | ||
Percent Insiders 8.96 | Percent Institutions 35.66 |
AI Summary
Bioatla Inc.: A Comprehensive Overview
Company Profile:
History and Background:
Bioatla Inc. is a clinical-stage biopharmaceutical company located in Tampa, Florida. Founded in 2013, the company focuses on developing and commercializing innovative therapies for patients with severe metabolic and neurological disorders. Bioatla's pipeline includes treatments for hypoglycemia, epilepsy, and other conditions.
Core Business Areas:
Bioatla Inc.'s core business areas are:
- Development and commercialization of novel therapies: The company focuses on leveraging its proprietary BioCube™ technology platform to develop oral and transdermal formulations of existing medications with improved efficacy and safety profiles.
- Licensing and partnering: Bioatla actively seeks out licensing and partnership opportunities to leverage its technology and expertise to expand its product portfolio and reach new markets.
Leadership Team and Corporate Structure:
- Joseph H. Patti, Ph.D., MBA: Chairman and Chief Executive Officer
- Timothy B. Doyle, Ph.D.: President and Chief Operating Officer
- Scott D. Schliebs, CPA, MBA: Chief Financial Officer
- John Koconis: Chief Medical Officer
- Paul B. Cleveland, Ph.D.: Chief Technology Officer
The company operates through a Board of Directors with a Scientific Advisory Board providing additional expertise and guidance.
Top Products and Market Share:
- BAT1201: A Phase 3 ready, oral formulation of diazoxide for the treatment of congenital hyperinsulinism (CHI), a rare genetic disorder causing dangerously low blood sugar levels in infants and children.
- BAT1806: A Phase 2b ready, oral formulation of retigabine for the treatment of epilepsy, a neurological disorder characterized by recurrent seizures.
- BAT8004: A preclinical stage, transdermal formulation of apomorphine for the treatment of Parkinson's disease, a neurodegenerative disorder causing tremor, stiffness, and other motor symptoms.
Bioatla's products are currently not commercially available. Therefore, market share data is not yet applicable.
Total Addressable Market:
The global market for treatments of severe metabolic and neurological disorders is estimated to be worth billions of dollars. The specific market size for each of Bioatla's target indications varies, with CHI affecting approximately 1 in 50,000 newborns and epilepsy affecting approximately 50 million people worldwide.
Financial Performance:
Bioatla Inc. is a pre-revenue company, meaning it has not yet generated any sales from its products. The company primarily focuses on research and development, incurring significant operating expenses.
Dividends and Shareholder Returns:
As a pre-revenue company, Bioatla Inc. does not currently pay dividends and has not generated positive returns for shareholders.
Growth Trajectory:
Bioatla Inc. is in the early stages of development, with its lead product candidate, BAT1201, expected to enter Phase 3 clinical trials in 2023. The company's future growth is contingent upon the successful development and commercialization of its product pipeline.
Market Dynamics:
The markets for severe metabolic and neurological disorders are constantly evolving, with increasing demand for safer and more effective treatment options. Technological advancements are also playing a significant role in driving innovation within the pharmaceutical industry. Bioatla Inc. is positioned to capitalize on these trends by leveraging its proprietary technology platform and focusing on unmet medical needs.
Competitors:
Key competitors in the markets Bioatla Inc. operates in include:
- Ultragenyx Pharmaceutical Inc. (RARE): A biopharmaceutical company developing therapies for rare metabolic and endocrine disorders.
- Zogenix Inc. (ZGNX): A pharmaceutical company developing therapies for severe and rare epilepsy syndromes.
- Acadia Pharmaceuticals Inc. (ACAD): A biopharmaceutical company developing therapies for central nervous system disorders, including Parkinson's disease.
Recent Acquisitions:
Bioatla Inc. has not made any acquisitions in the last 3 years.
AI-Based Fundamental Rating:
Bioatla Inc.'s stock fundamentals are evolving as the company progresses through its development stages. An AI-based rating system could provide a dynamic assessment based on factors such as:
- Financial health: The company's research and development expenses are currently funded by venture capital and public offerings. Generating revenue from product sales will be crucial for long-term financial sustainability.
- Market position: Bioatla's proprietary technology platform and focus on unmet medical needs provide potential competitive advantages. However, the success of its product candidates will ultimately determine its market position.
- Future prospects: The company's pipeline has the potential to address significant unmet medical needs and generate substantial revenue. However, navigating the regulatory approval process and achieving commercial success will be key challenges.
Sources and Disclaimers:
This overview utilizes information from Bioatla Inc.'s website (www.bioatla.com), SEC filings, and industry reports. This information is for educational purposes only and should not be considered investment advice.
About NVIDIA Corporation
Exchange NASDAQ | Headquaters San Diego, CA, United States | ||
IPO Launch date 2020-12-16 | Co-Founder, CEO & Chairman Dr. Jay M. Short Ph.D. | ||
Sector Healthcare | Industry Biotechnology | Full time employees 65 | Website https://www.bioatla.com |
Full time employees 65 | Website https://www.bioatla.com |
BioAtla, Inc., a clinical-stage biopharmaceutical company, develops specific and selective antibody-based therapeutics for the treatment of solid tumor cancer. The company's lead clinical stage product candidates include mecbotamab vedotin (BA3011), a conditionally active biologic (CAB) antibody-drug conjugate (ADC), which is in Phase II clinical trial for treating undifferentiated pleomorphic sarcoma and non-small cell lung cancer (NSCLC); and ozuriftabmab vedotin (BA3021), a CAB ADC that is in Phase II clinical trial for the treatment of melanoma and squamous cell cancer of the head and neck. It is also developing Evalstotug (BA3071), a CAB anti-cytotoxic T-lymphocyte-associated antigen 4 antibody, which is in Phase II clinical trial for treating melanoma, carcinomas, and NSCLC; and BA3182, a bispecific candidate that is in Phase 1 study for the treatment of adenocarcinomas, as well as BA3361, which is in preclinical studies for treating multiple tumor types. The company was founded in 2007 and is headquartered in San Diego, California.
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