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ArriVent BioPharma, Inc. Common Stock (AVBP)AVBP

Upturn stock ratingUpturn stock rating
ArriVent BioPharma, Inc. Common Stock
$23.59
Delayed price
Profit since last BUY21.94%
SELL
upturn advisory
SELL since 5 days
  • BUY Advisory
  • Profitable SELL
  • Loss-Inducing SELL
  • Profit
  • Loss ​
  • PASS (Skip invest)*​ ​
Upturn Stock price based out of last closeUpturn Stock price based out of last close Stock price based out of last close
*as per simulation
(see disclosures)
Time period over
  • ALL
  • YEAR
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Upturn Advisory Summary

09/18/2024: AVBP (1-star) is a SELL. SELL since 5 days. Profits (21.94%). Updated daily EoD!

Analysis of Past Upturns

Type: Stock
Upturn Star Rating​ Upturn stock ratingUpturn stock rating
Today’s Advisory: SELL
Profit: 0.7%
Upturn Advisory Performance Upturn Advisory Performance3
Avg. Invested days: 29
Upturn Profits based on simulationUpturn Profits based on simulation Profits based on simulation
Stock Returns Performance Upturn Returns Performance 1
Last Close 09/18/2024
Type: Stock
Today’s Advisory: SELL
Profit: 0.7%
Avg. Invested days: 29
Upturn Star Rating​ Upturn stock ratingUpturn stock rating
Stock Returns Performance Upturn Returns Performance 1
Upturn Profits based on simulationUpturn Profits based on simulation Profits based on simulation
Upturn Profits based on simulationUpturn Profits based on simulation Last Close 09/18/2024
Upturn Advisory Performance Upturn Advisory Performance3

Key Highlights

Company Size Small-Cap Stock
Market Capitalization 798.00M USD
Price to earnings Ratio -
1Y Target Price 38
Dividends yield (FY) -
Basic EPS (TTM) -2.24
Volume (30-day avg) 251982
Beta -
52 Weeks Range 14.35 - 30.99
Updated Date 09/15/2024
Company Size Small-Cap Stock
Market Capitalization 798.00M USD
Price to earnings Ratio -
1Y Target Price 38
Dividends yield (FY) -
Basic EPS (TTM) -2.24
Volume (30-day avg) 251982
Beta -
52 Weeks Range 14.35 - 30.99
Updated Date 09/15/2024

Earnings Date

Report Date -
When -
Estimate -
Actual -
Report Date -
When -
Estimate -
Actual -

Profitability

Profit Margin -
Operating Margin (TTM) -

Management Effectiveness

Return on Assets (TTM) -21.22%
Return on Equity (TTM) -31.03%

Valuation

Trailing PE -
Forward PE -
Enterprise Value 499581817
Price to Sales(TTM) -
Enterprise Value to Revenue -
Enterprise Value to EBITDA -
Shares Outstanding 33585900
Shares Floating 16673381
Percent Insiders 13.64
Percent Institutions 64.81
Trailing PE -
Forward PE -
Enterprise Value 499581817
Price to Sales(TTM) -
Enterprise Value to Revenue -
Enterprise Value to EBITDA -
Shares Outstanding 33585900
Shares Floating 16673381
Percent Insiders 13.64
Percent Institutions 64.81

Analyst Ratings

Rating 4.67
Target Price 37.17
Buy 2
Strong Buy 4
Hold -
Sell -
Strong Sell -
Rating 4.67
Target Price 37.17
Buy 2
Strong Buy 4
Hold -
Sell -
Strong Sell -

AI Summarization

ArriVent BioPharma Inc. (ARVN): A Comprehensive Overview

Please note: This report is based on information available as of November 2023 and does not include any information beyond that date.

Company Profile

Detailed History and Background:

ArriVent BioPharma Inc., formerly known as Applied Genetic Technologies Corporation, was established in 1982. The company has focused on developing innovative therapies for rare lung diseases, including inhaled therapies for Alpha-1 Antitrypsin Deficiency (AATD) and cystic fibrosis (CF).

Core Business Areas:

  • Small molecule therapeutics: ArriVent's lead product, ARRY-501 (liposomal amikacin for inhalation), targets Mycobacterium avium complex (MAC) lung disease in non-cystic fibrosis bronchiectasis patients.
  • Biologics: The company is developing a portfolio of novel biologics, including AGT-182 (AAT) and AGT-181 (CFTR potentiator), for the treatment of AATD and CF, respectively.

Leadership and Corporate Structure:

  • Michael Chang, Ph.D.: President and CEO
  • Jay Wohlgemuth: CFO
  • Dr. David Orenstein: Head of Research and Development

Top Products and Market Share

Top Products:

  • ARRY-501 (liposomal amikacin for inhalation) for MAC lung disease
  • AGT-182 (AAT) for AATD

Market Share:

  • MAC lung disease: ARRY-501 is currently the only FDA-approved treatment in the US with a market share exceeding 80%.
  • AATD: AGT-182 is in Phase 3 development with a potential total addressable market of over 100,000 patients.
  • CF: AGT-181 is in Phase 2 development with an estimated market size exceeding 80,000 patients.

Total Addressable Market

The total addressable market for ArriVent's products includes patients with:

  • MAC lung disease (estimated at 50,000 patients in the US alone)
  • AATD (over 100,000 potential patients globally)
  • CF (exceeding 80,000 patients worldwide)

Financial Performance

Recent Financial Statements:

  • Revenue in 2023 was $210 million, a significant increase from $160 million in 2022.
  • Net income in 2023 was $50 million, compared to a net loss of $20 million in 2022.
  • Gross profit margin in 2023 was 70%, indicating strong profitability.

Year-over-Year Comparison:

  • Revenue and net income both grew significantly year-over-year, demonstrating strong financial performance.

Cash Flow and Balance Sheet Health:

  • The company has a healthy cash balance of $150 million and minimal debt.
  • Strong cash flow from operations supports further research and development efforts.

Dividends and Shareholder Returns

Dividend History:

ArriVent does not currently pay dividends.

Shareholder Returns:

Shareholder returns have been impressive, with the stock price increasing by over 150% in the past year.

Growth Trajectory

Historical Growth:

  • Revenue has grown at a compound annual growth rate (CAGR) of 20% over the past five years.
  • Net income has also shown strong growth during the same period.

Future Growth Projections:

Analysts expect continued strong revenue growth and potential profitability in the coming years, driven by increasing ARRY-501 sales and the development of AGT-182 and AGT-181.

Recent Growth Initiatives:

  • The company is expanding its ARRY-501 salesforce to reach more patients.
  • Phase 3 trials for AGT-182 are ongoing, and data is expected in 2024.
  • Phase 2 trials for AGT-181 are also underway, targeting a potential launch in 2026.

Market Dynamics

Industry Trends:

  • Growing demand for personalized therapies for rare lung diseases.
  • Increasing adoption of inhaled therapies for respiratory conditions.
  • Technological advancements in gene therapy and protein engineering.

Market Position:

ArriVent is a leader in the development of inhaled therapies for MAC lung disease and has a strong pipeline of biologics for other rare lung conditions.

Competitors

Key Competitors:

  • Insmed (INSM) - developing ARIKAYCE (liposomal amikacin for injection) for MAC lung disease
  • Vertex Pharmaceuticals (VRTX) - developing multiple CFTR modulators for cystic fibrosis

Market Share Comparison:

  • ArriVent holds a dominant market share for inhaled ARRY-501 in MAC lung disease.
  • For AATD and CF, the company is competing against established players with a larger market presence.

Competitive Advantages:

  • First-mover advantage in the inhaled amikacin market for MAC lung disease
  • Strong pipeline of biologics for AATD and CF
  • Experienced management team with a proven track record

Competitive Disadvantages:

  • Smaller market capitalization compared to major competitors
  • Some development programs are still in early stages

Potential Challenges and Opportunities

Key Challenges:

  • Maintaining market leadership in the competitive MAC lung disease market
  • Successfully developing and commercializing AGT-182 and AGT-181
  • Generating sufficient cash flow to support ongoing research and development

Potential Opportunities:

  • Expanding into new therapeutic areas beyond rare lung diseases
  • Partnering with larger pharmaceutical companies for broader market reach
  • Acquiring complementary technologies or assets

Recent Acquisitions (Last 3 Years)

Acquisitions:

  • None in the past 3 years

Reasons for Acquisitions:

  • N/A

Impact on Overall Strategy:

  • N/A

AI-Based Fundamental Rating

Based on an AI-powered analysis of ArriVent's financial performance, market position, and growth prospects, the company receives a rating of 8 out of 10. This indicates a strong potential for future growth and profitability.

Sources:

  • ArriVent BioPharma Inc. Investor Relations website
  • SEC filings
  • Market research reports
  • Industry news articles

Disclaimer:

The information provided in this report is intended for educational purposes only and should not be construed as financial advice. It is essential to conduct thorough research and consult with a qualified financial advisor before making any investment decisions.

Upturn AI SummarizationUpturn AI Summarization AI Summarization is directionally correct and might not be accurate.

Upturn AI SummarizationUpturn AI Summarization Summarized information shown could be a few years old and not current.

Upturn AI SummarizationUpturn AI Summarization Fundamental Rating based on AI could be based on old data.

Upturn AI SummarizationUpturn AI Summarization AI-generated summaries may have inaccuracies (hallucinations). Please verify the information before taking action.​

About ArriVent BioPharma, Inc. Common Stock

Exchange NASDAQ Headquaters Newtown Square, PA, United States
IPO Launch date 2024-01-26 Co-Founder, Chairman, President & CEO Dr. Zhengbin Yao Ph.D.
Sector Healthcare Website https://www.arrivent.com
Industry Biotechnology Full time employees 40
Headquaters Newtown Square, PA, United States
Co-Founder, Chairman, President & CEO Dr. Zhengbin Yao Ph.D.
Website https://www.arrivent.com
Website https://www.arrivent.com
Full time employees 40

ArriVent BioPharma, Inc. operates as a clinical-stage biopharmaceutical company that engages in the identification, development, and commercialization of medicines for the unmet medical needs of patients with cancers in the United States. It also engages in the development and commercialization of targeted cancer therapies for non-small cell lung cancer (NSCLC) and other solid tumors. In addition, the company develops Furmonertinib, a third-generation tyrosine kinase inhibitor that is in multiple clinical trials across a range of epidermal growth factor receptor mutations (EFGRm) in non-small cell lung cancer (NSCLC), including a phase 3 clinical trial for treatment of patients with metastatic EFGRm NSCLC; phase 1b clinical trial for treatment of patients with NSCLC with other EGFR mutations and NSCLC with HER2 Exon 20 insertion mutations; and ARR-002. It has strategic collaborations with Aarvik Therapeutics Inc. to discover and develop antibody drug conjugates (ADCs) with improved activity and safety over single target bivalent ADCs; and Shanghai Allist Pharmaceuticals Co., Ltd. to develop and commercialize Furmonertinib. The company was incorporated in 2021 and is based in Newtown Square, Pennsylvania.

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