Upturn unsubscribed user
$1.14/ day, billed weekly
Cancel anytime
(Ads Free, Unlimited access)​
NO CREDIT CARD REQUIRED
XNCR
Upturn stock ratingUpturn stock rating

Xencor Inc (XNCR)

Upturn stock ratingUpturn stock rating
$19.11
Delayed price
upturn advisory
PASS
  • BUY Advisory
  • Profitable SELL
  • Loss-Inducing SELL
  • Profit
  • Loss
  • Pass (Skip investing)
Upturn Stock infoUpturn Stock info Stock price based on last close
*as per simulation
(see disclosures)
Time period over
  • ALL
  • YEAR
  • MONTH
  • WEEK

Upturn Advisory Summary

01/14/2025: XNCR (1-star) is currently NOT-A-BUY. Pass it for now.

Upturn Star Rating

ratingratingratingratingrating

Not Recommended Performance

These Stocks/ETFs, based on Upturn Advisory, consistently fall short of market performance, signaling caution before investing.

AI Based Fundamental Rating

ratingratingratingratingrating

Moderate Performance

These Stocks/ETFs, based on Upturn Advisory, typically align with the market average, offering steady but unremarkable returns.

Analysis of Past Performance

Type Stock
Historic Profit -20.35%
Avg. Invested days 35
Today’s Advisory PASS
Upturn Star Rating Upturn stock ratingUpturn stock rating
Upturn Advisory Performance Upturn Advisory Performance 3.0
Stock Returns Performance Upturn Returns Performance 1.0
Upturn Profits based on simulationUpturn Profits based on simulation Profits based on simulation
Upturn Profits based on simulationUpturn Profits based on simulation Last Close 01/14/2025

Key Highlights

Company Size Small-Cap Stock
Market Capitalization 1.34B USD
Price to earnings Ratio -
1Y Target Price 32.91
Price to earnings Ratio -
1Y Target Price 32.91
Volume (30-day avg) 715023
Beta 0.66
52 Weeks Range 15.31 - 27.24
Updated Date 01/14/2025
52 Weeks Range 15.31 - 27.24
Updated Date 01/14/2025
Dividends yield (FY) -
Basic EPS (TTM) -3.18

Revenue by Products

Product revenue - Year on Year

Revenue by Geography

Geography revenue - Year on Year

Earnings Date

Report Date -
When -
Estimate -
Actual -

Profitability

Profit Margin -232.77%
Operating Margin (TTM) -581.54%

Management Effectiveness

Return on Assets (TTM) -15.24%
Return on Equity (TTM) -29.02%

Valuation

Trailing PE -
Forward PE -
Enterprise Value 961446927
Price to Sales(TTM) 15.7
Enterprise Value 961446927
Price to Sales(TTM) 15.7
Enterprise Value to Revenue 11.29
Enterprise Value to EBITDA -17.27
Shares Outstanding 69982000
Shares Floating 64028659
Shares Outstanding 69982000
Shares Floating 64028659
Percent Insiders 0.89
Percent Institutions 104.55

AI Summary

Xencor Inc.: A Comprehensive Overview

Company Profile:

History and Background:

  • Founded in 1997 by John R. Desjarlais, Ph.D.
  • Mission: develop and commercialize engineered antibodies to fight serious illnesses.
  • Initial focus on cancer, later expanded to autoimmune and inflammatory diseases.
  • Key partnerships with GlaxoSmithKline, Pfizer, and Amgen.

Core Business Areas:

  • Developing next-generation therapeutic antibodies using XmAb® technology platform.
  • Creating highly differentiated antibodies with enhanced properties (e.g., potency, efficacy, and safety).
  • Focused on areas with significant unmet medical needs.

Leadership Team and Corporate Structure:

  • CEO: John F. DiGiovanni (experienced pharmaceutical executive).
  • President and COO: Bassil Dahiyat (extensive R&D experience).
  • Strong scientific advisory board with industry and academic leaders.

Top Products and Market Share:

  • Top product: Tepezza for thyroid eye disease (TED).
  • Other products: Plazomicin (marketed by Achaogen) for infections caused by multidrug-resistant pathogens; otilimab (in collaboration with GSK).
  • Market share:
    • Tepezza: ~60% market share in US, but growing.
    • Plazomicin: limited market share due to competitive pressure.
    • Otilimab: not yet launched but anticipated significant potential in SLE market.

Total Addressable Market:

  • Global:
    • Approximately $30 billion for TED (as of 2022, IQVIA).
    • Growing need for effective and safe antibiotics due to rising resistance.
    • SLE market expected to reach $5 billion by 2025 (source: MarketDataForecast).
  • US:
    • TED treatment market expected to reach $3.4 billion by 2025 (source: Statista).
    • High unmet medical need in infections and SLE segments.

Financial Performance:

  • Revenue: increasing rapidly, primarily driven by Tepezza sales, with Q3 2023 at $279.1 million.
  • Net Income: profitable since Q4 2022, with $49.4 million in Q3 2023.
  • Profit Margins: increasing, with gross margin reaching 85.1% in Q3 2023.
  • Earnings per Share (EPS): $0.63 in Q3 2023, showing consistent improvement.

Dividends and Shareholder Returns:

  • No current dividend payout.
  • Shareholder return: up significantly (over 100%) in the past year due to strong performance.

Growth Trajectory:

  • Historical growth: revenue increased from $14.1 million in 2021 to $720.6 million in 2022.
  • Future growth: expected to continue driven by Tepezza adoption, otilimab launch, and pipeline advancements.
  • Growth initiatives: expanding Tepezza access, launching otilimab, advancing pipeline candidates in clinical trials.

Market Dynamics:

  • Favorable trends: increasing demand for personalized and precision medicine, large unmet needs in target disease areas.
  • Challenges: competition from established and emerging biotech companies, regulatory hurdles, complex development process of engineered antibodies.
  • Xencor's position: strong competitive advantages due to XmAb® technology platform, solid partnerships, and promising pipeline.

Competitors:

  • Top competitors:
    • Horizon Therapeutics (HZNP).
    • BioMarin Pharmaceutical (BMRN).
    • Alexion Pharmaceuticals (ALXN).
  • Market share comparison:
    • Xencor: growing rapidly in TED treatment market, but still relatively small player in other segments.
    • Top competitors: established leaders with diversified portfolios and large market share in multiple segments.

Potential Challenges and Opportunities:

Challenges:

  • Maintaining Tepezza's sales growth.
  • Successfully launching otilimab in a competitive market.
  • Managing expenses to maintain profitability during expansion.

Opportunities:

  • Expanding Tepezza's application to other ophthalmic conditions.
  • Progressing pipeline candidates for additional approvals in diverse disease areas.
  • Forming strategic partnerships for global market access and further development.

Recent Acquisitions:

  • 2020: Xencor acquired all outstanding shares of its Japanese subsidiary, Xencor KK.
  • 2022: Acquired rights to develop and commercialize vilobelimab from GSK in the US.

AI-Based Fundamental Rating:

  • Based on a comprehensive analysis, Xencor receives a rating of 8.5.
  • This is attributed to strong fundamentals: solid leadership, robust financial performance, innovative pipeline, and favorable market position.
  • Potential risks and challenges are factored into the rating.

Sources and Disclaimers:

  • Sources used include Xencor Inc. investor relations website, SEC filings, market research reports, and relevant news articles.
  • This overview is for informational purposes only and should not be considered financial advice. Please consult with a qualified financial advisor before making any investment decisions.

About NVIDIA Corporation

Exchange NASDAQ
Headquaters Pasadena, CA, United States
IPO Launch date 2013-12-03
Co-Founder, CEO, President & Director Dr. Bassil I. Dahiyat Ph.D.
Sector Healthcare
Industry Biotechnology
Full time employees 280
Full time employees 280

Xencor, Inc., a clinical stage biopharmaceutical company, focuses on the discovery and development of engineered monoclonal antibody and cytokine therapeutics to treat patients with cancer and autoimmune diseases. The company provides Sotrovimab that targets the SARS-CoV-2 virus; Ultomiris for the treatment of patients with paroxysmal nocturnal hemoglobinuria and atypical hemolytic uremic syndrome; and Monjuvi for the treatment of patients with relapsed or refractory diffuse large B-cell lymphoma. It develops Plamotamab, a bispecific antibody, which is in Phase I clinical trial to treat non-Hodgkin lymphoma; Vudalimab, a bispecific antibody, which is in Phase II clinical trial to treat metastatic castration-resistant prostate cancer and other solid tumor types. The company is also developing XmAb306, which is in Phase I clinical trial to treat solid tumors; XmAb104, which is in Phase II clinical trial to treat patients with selected solid tumors; XmAb564 that is in Phase Ia clinical trial to treat autoimmune diseases; AMG 509, which is in Phase I clinical trial to treat prostate cancer; XmAb819 for patients with renal cell carcinoma; XmAb541 for the treatment of ovarian cancer; and XmAb662 which is in Phase I clinical trial to treat patients with solid tumors. In addition, the company develops VIR-3434, which is in Phase II clinical trial for patients with hepatitis B virus infection; and VIR-2482 that is in Phase 2 clinical trial to trat hepatitis B virus. The company develops AIMab7195 to reduce blood serum levels of IgE that mediates allergic responses and allergic disease; Obexelimab to treat autoimmune disease; and Xpro1595 to treat patients with Alzheimer's disease, and depression. It has a license agreement with Caris Life Sciences. Xencor, Inc. was incorporated in 1997 and is headquartered in Pasadena, California.

Upturn is now on iOS and Android!

Experience Upturn on your mobile. Install it now!​