AzurRx BioPharma, Inc. (AZRX) Stock Analysis
DELISTED 2021
What happened to AzurRx BioPharma, Inc. (AZRX) stock?
AzurRx BioPharma, Inc. (AZRX) no longer trades on public markets. It was delisted in September 2021. The figures below are historical and are not a current quote.
For informational purposes only. Not financial advice. Analysis by Sedat ANAK, Founder & Editor-in-Chief | AI-powered analysis. Data sourced from SEC filings and institutional-grade financial providers. Editorially reviewed. Not financial advice.
AzurRx BioPharma, Inc. (AZRX) trades at $3.45. AzurRx BioPharma, Inc. is a biotechnology company focused on developing non-systemic biologics for gastrointestinal disorders. Market cap: $3.43M, Sector: Healthcare.
Last analyzed: Mar 15, 2026Analyst Coverage for AZRX: AZRX does not currently have published analyst price targets in our coverage universe. This is common for smaller-cap names with limited Wall Street coverage. In the absence of analyst consensus, our AI model evaluates AZRX against Healthcare peers across nine fundamental dimensions and assigns a neutral fundamental signal based on the underlying data.
AZRX: 2/2 scored disciplines lean bullish. Dominant signal: Ken Griffin bullish.
How is this calculated? →AzurRx BioPharma, Inc. (AZRX) Healthcare & Pipeline Overview
AzurRx BioPharma, Inc. is a clinical-stage biotechnology company specializing in the development of non-systemic biologics targeting gastrointestinal disorders, including exocrine pancreatic insufficiency and antibiotic-associated diarrhea. Their pipeline focuses on addressing unmet needs in GI health through innovative therapeutic proteins, positioning them in a competitive biotechnology landscape.
What Is the Investment Thesis for AZRX?
AzurRx BioPharma presents a high-risk, high-reward investment opportunity within the biotechnology sector. The company's focus on non-systemic biologics for GI disorders addresses a significant market need. Successful clinical trials and regulatory approvals for MS1819 and AZX1101 could drive substantial value. Key value drivers include positive clinical data readouts, strategic partnerships, and potential acquisition by a larger pharmaceutical company. The company's small size and limited resources pose risks, including potential delays in clinical development and the need for additional financing. The P/E ratio of 0.20 indicates potential undervaluation, but this must be considered in the context of the company's developmental stage and inherent risks.
Based on FMP financials and quantitative analysis
AZRX Key Highlights
AzurRx BioPharma is focused on developing non-systemic biologics for gastrointestinal disorders, addressing a significant unmet medical need.
- The company's lead product candidate, MS1819, targets exocrine pancreatic insufficiency (EPI), a condition associated with chronic pancreatitis and cystic fibrosis.
- AZX1101, another key pipeline asset, is being developed for the prevention of hospital-acquired infections and antibiotic-associated diarrhea.
- The company's market capitalization is $0.00B, reflecting its early-stage development status.
- AzurRx BioPharma operates with a small team of 12 employees, indicating a lean operational structure.
Who Are AZRX's Competitors?
AZRX is benchmarked below against 8 industry peers on price, market cap, and our AI MoonshotScore.
| Company | Price | Change | Market Cap | AI Score |
|---|---|---|---|---|
| LSTA Lisata Therapeutics, Inc. | $1.12 | +0.00% | $10.2M | — |
| ADAPY Adaptimmune Therapeutics plc | $0.03 | +0.00% | $7.16M | 72 |
| RLYB Rallybio Corporation | $16.60 | -2.35% | $88.1M | 81 |
| ICCC ImmuCell Corporation | $10.09 | -0.39% | $91.3M | 77 |
| JNCE Jounce Therapeutics, Inc. | $1.88 | +0.00% | $99.0M | 71 |
| ORMP Oramed Pharmaceuticals Inc. | $4.79 | +0.00% | $196M | 77 |
| CGEN Compugen Ltd. | $2.65 | +8.61% | $251M | 76 |
| NAGE Niagen Bioscience Inc | $3.15 | -0.63% | $251M | 74 |
AI Score by Stock Expert AI · Price data: FMP / Yahoo Finance
What Are AZRX's Key Strengths?
Novel non-systemic biologics approach.
- Pipeline focused on unmet needs in GI disorders.
- Potential for targeted therapies with fewer side effects.
- Experienced management team.
What Are AZRX's Weaknesses?
Limited financial resources.
- Small team size.
- Dependence on successful clinical trials.
- High regulatory risk.
What Could Drive AZRX Stock Higher?
MS1819 Phase 3 clinical trial data readout for exocrine pancreatic insufficiency (EPI).
- AZX1101 clinical trial initiation for the prevention of hospital-acquired infections.
- Potential strategic partnerships with larger pharmaceutical companies.
- Regulatory discussions with the FDA regarding MS1819 and AZX1101 development pathways.
What Are the Key Risks for AZRX?
Financial-distress signal — its Altman Z-Score of -6.39 sits in the distress zone (elevated bankruptcy risk).
- Negative return on equity (-49.8%) — the business is not currently generating profit on shareholder capital.
- Weak fundamentals — a Piotroski F-Score of 3/9 flags soft profitability, leverage or efficiency.
- Clinical trial failures for MS1819 or AZX1101.
- Regulatory delays or rejection of MS1819 or AZX1101.
- Competition from established pharmaceutical companies with greater resources.
- Dependence on securing additional funding to support clinical development.
- Intellectual property challenges or patent infringement claims.
What Are the Growth Opportunities for AZRX?
- MS1819 Clinical Development: A significant growth opportunity lies in the successful clinical development and commercialization of MS1819 for the treatment of exocrine pancreatic insufficiency (EPI). Positive Phase 3 trial results and subsequent regulatory approval could establish MS1819 as a leading therapy in this space, capturing a substantial market share within the next 3-5 years.
- AZX1101 for Infection Prevention: The development of AZX1101 for the prevention of hospital-acquired infections and antibiotic-associated diarrhea represents another key growth driver. With rising concerns about antibiotic resistance and the increasing incidence of nosocomial infections, AZX1101 has the potential to address a critical unmet need. Successful clinical trials and regulatory approval could position AZX1101 as a valuable tool in infection control, generating significant revenue streams within 5 years.
- Strategic Partnerships: Forming strategic partnerships with larger pharmaceutical companies could accelerate the development and commercialization of AzurRx's pipeline assets. Collaborations could provide access to additional funding, expertise, and distribution networks, enhancing the company's ability to bring its therapies to market. Securing such partnerships within the next 1-2 years would be a major catalyst for growth.
- Expansion of Pipeline: Expanding the company's pipeline through the acquisition or in-licensing of additional GI-focused therapies could diversify its product portfolio and reduce reliance on MS1819 and AZX1101. Identifying and securing promising new assets within the next 2-3 years would strengthen AzurRx's long-term growth prospects.
- Orphan Drug Designation: Pursuing orphan drug designation for MS1819 in specific patient populations could provide regulatory and commercial advantages, including market exclusivity and tax incentives. Obtaining orphan drug designation within the next year would enhance the attractiveness of MS1819 and support its development and commercialization efforts.
What Are AZRX's Competitive Advantages?
- Proprietary technology in developing non-systemic biologics.
- Patent protection for MS1819 and AZX1101.
- Clinical data supporting the safety and efficacy of their drug candidates.
- First-mover advantage in specific GI disorder treatments, if approved.
What Does AZRX Do?
AzurRx BioPharma, Inc., headquartered in Brooklyn, New York, is a biopharmaceutical company dedicated to the research and development of non-systemic biologics for the treatment of gastrointestinal (GI) disorders. Founded with the goal of addressing unmet medical needs in GI health, the company focuses on developing therapies that act locally within the GI tract to minimize systemic side effects. AzurRx's current product pipeline features two therapeutic proteins: MS1819 and AZX1101. MS1819 is an acid-resistant lipase intended for the treatment of exocrine pancreatic insufficiency (EPI), a condition often associated with chronic pancreatitis and cystic fibrosis. The company is developing MS1819 using recombinant DNA technology to produce a stable and effective enzyme replacement therapy. AZX1101 is a recombinant-lactamase combination under development for the prevention of hospital-acquired infections caused by resistant bacterial strains induced by parenteral administration of beta-lactam antibiotics, as well as the prevention of antibiotic-associated diarrhea (AAD). By focusing on non-systemic biologics, AzurRx aims to provide targeted therapies with improved safety profiles for patients suffering from debilitating GI conditions. The company currently employs 12 full-time employees and is navigating the complex regulatory landscape to advance its pipeline towards commercialization.
What Products and Services Does AZRX Offer?
- Develop non-systemic biologics for gastrointestinal disorders.
- Research and develop MS1819 for the treatment of exocrine pancreatic insufficiency (EPI).
- Develop AZX1101 for the prevention of hospital-acquired infections and antibiotic-associated diarrhea.
- Utilize recombinant DNA technology to produce therapeutic proteins.
- Conduct clinical trials to evaluate the safety and efficacy of their drug candidates.
- Seek regulatory approvals from agencies like the FDA to commercialize their products.
How Does AZRX Make Money?
- Focus on research and development of novel therapies.
- Outsource manufacturing and clinical trial operations.
- Seek partnerships with larger pharmaceutical companies for commercialization.
- Generate revenue through product sales and licensing agreements, if approved.
What Industry Does AZRX Operate In?
The biotechnology industry is characterized by high R&D spending, lengthy regulatory approval processes, and intense competition. Companies like AzurRx BioPharma operate in a landscape where innovation and clinical success are paramount. The market for GI disorder treatments is substantial, driven by increasing prevalence of conditions like EPI and antibiotic-resistant infections. Competition includes both established pharmaceutical companies and other emerging biotech firms developing novel therapies. Success hinges on demonstrating clinical efficacy, securing regulatory approvals, and establishing commercial partnerships.
Who Are AZRX's Key Customers?
- Patients suffering from exocrine pancreatic insufficiency (EPI).
- Hospitals and healthcare providers seeking to prevent hospital-acquired infections.
- Patients at risk of antibiotic-associated diarrhea (AAD).
- Pharmaceutical companies interested in licensing or acquiring novel GI therapies.
AzurRx BioPharma, Inc. (AZRX) Valuation Context
Valued at $3.43M, AZRX is classified as a micro-cap stock.
AZRX Revenue & Earnings Trend
In Q1 2026, AZRX generated $38K in top-line revenue, marking a sequential increase of 5.4%. The company recorded a net loss of $3.4M, with diluted EPS of $-0.82.
Company Profile
AzurRx BioPharma, Inc. operates in the Biotechnology industry within the Healthcare sector. It is headquartered in Brooklyn, US. The company is led by CEO James Sapirstein. AZRX has traded publicly since 2016.
Key Financial Metrics
Return on equity for AzurRx BioPharma, Inc. stands at -49.8%, a gauge of how efficiently it converts shareholder capital into profit. Return on assets is -18.2%, showing how much profit it generates from its asset base. A current ratio of 0.16 means current liabilities exceed short-term assets, a liquidity point worth watching. Its earnings yield is -56.9%, the inverse of the P/E and a quick read on earnings relative to price.
Financial Health
AzurRx BioPharma, Inc.'s Piotroski F-Score is 3/9, a 9-point checklist of profitability, leverage and efficiency — flagging fundamental weakness worth scrutiny. Its Altman Z-Score of -6.39 places it in the distress zone, a signal of elevated financial risk.
AZRX Financials
Fundamental Snapshot
Based on FMP financials and quantitative analysis · FY 2025
Bull Case vs Bear Case
Bull Case
- Novel non-systemic biologics approach.
- Pipeline focused on unmet needs in GI disorders.
- Potential for targeted therapies with fewer side effects.
- Experienced management team.
Bear Case
- Limited financial resources.
- Small team size.
- Dependence on successful clinical trials.
- High regulatory risk.
AI-generated arguments based on insider flow, news sentiment and technicals — not financial advice · August 2026
Recent Quarterly Results
| Quarter | Revenue | Net Income | EPS |
|---|---|---|---|
| Q1 2026 | $38,208 | -$3M | -$0.82 |
| Q4 2025 | $36,251 | -$3M | -$2.92 |
Based on FMP financials and quantitative analysis
AZRX Latest News
No recent news available for AZRX.
Leadership: James Sapirstein
CEO
James Sapirstein serves as the CEO of AzurRx BioPharma, Inc. His career spans several decades in the pharmaceutical and biotechnology industries, with a focus on commercialization and strategic development. Prior to joining AzurRx, he held leadership positions at various companies, including roles in sales, marketing, and business development. Sapirstein's experience includes launching and managing pharmaceutical products across multiple therapeutic areas. He brings a wealth of knowledge in navigating the complexities of the pharmaceutical market and driving growth for emerging companies.
Track Record: Under James Sapirstein's leadership, AzurRx BioPharma has focused on advancing its pipeline of non-systemic biologics for gastrointestinal disorders. Key milestones include progressing MS1819 and AZX1101 through clinical development stages and securing funding to support these efforts. Sapirstein's strategic decisions have aimed at maximizing the value of the company's assets and positioning it for potential partnerships or acquisitions.
AzurRx BioPharma, Inc. Healthcare Stock: Key Questions Answered
What happened to AzurRx BioPharma, Inc. (AZRX) stock?
AzurRx BioPharma, Inc. (AZRX) no longer trades on public markets. It was delisted in September 2021. The figures below are historical and are not a current quote.
Can I still buy AZRX shares?
No. AZRX stopped trading on public markets in September 2021, so the shares are not available through a broker. Anything you see quoted for AZRX elsewhere is historical data, not a live market.
Are the figures on this page current?
No. Every number here is the last value recorded before AZRX stopped trading. Nothing on this page updates, and none of it is a current quote.
Why does this page still exist?
Because people still search for what happened to AzurRx BioPharma, Inc.. An archived profile that states the delisting plainly is more useful than a dead link — provided it is labelled as history, which is what this page does.
What does AzurRx BioPharma, Inc. do?
AzurRx BioPharma, Inc. is a biotechnology company focused on the development of non-systemic biologics for the treatment of gastrointestinal (GI) disorders. The company's lead product candidates, MS1819 and AZX1101, target exocrine pancreatic insufficiency (EPI) and hospital-acquired infections, respectively.
What are the main risks for AZRX?
The main risks for AzurRx BioPharma, Inc. include clinical trial failures, regulatory setbacks, and competition from established pharmaceutical companies. The success of the company hinges on the positive outcomes of clinical trials for MS1819 and AZX1101. Regulatory delays or rejection by the FDA could significantly impact the company's prospects.
What is AzurRx BioPharma, Inc.'s drug pipeline status?
AzurRx BioPharma, Inc.'s drug pipeline consists of two main therapeutic proteins: MS1819 and AZX1101. MS1819 is being developed for the treatment of exocrine pancreatic insufficiency (EPI) associated with chronic pancreatitis and cystic fibrosis, with ongoing clinical trials to assess its efficacy.
How does AzurRx BioPharma, Inc. navigate regulatory approval processes?
AzurRx BioPharma, Inc. navigates regulatory approval processes by conducting rigorous clinical trials to demonstrate the safety and efficacy of its drug candidates. The company works closely with regulatory agencies like the FDA to ensure compliance with all applicable regulations and guidelines. This includes submitting detailed clinical trial data, manufacturing information, and safety reports.
Disclaimer: This content is for informational purposes only and does not constitute investment advice. Always do your own research and consult a financial advisor.
Official Resources
Data provided for informational purposes only.
- AI analysis pending; information based on available company data.
- Market Cap is very low, indicating a micro-cap stock with higher volatility.