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Corcept Therapeutics Incorporated (CORT)

Upturn stock ratingUpturn stock rating
$51.66
Delayed price
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PASS
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Upturn Advisory Summary

01/14/2025: CORT (3-star) is currently NOT-A-BUY. Pass it for now.

Upturn Star Rating

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Moderate Performance

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

AI Based Fundamental Rating

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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 16.47%
Avg. Invested days 31
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 2.0
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 Mid-Cap Stock
Market Capitalization 5.35B USD
Price to earnings Ratio 39.58
1Y Target Price 74.9
Price to earnings Ratio 39.58
1Y Target Price 74.9
Volume (30-day avg) 803880
Beta 0.46
52 Weeks Range 20.84 - 62.22
Updated Date 01/13/2025
52 Weeks Range 20.84 - 62.22
Updated Date 01/13/2025
Dividends yield (FY) -
Basic EPS (TTM) 1.29

Earnings Date

Report Date -
When -
Estimate -
Actual -

Profitability

Profit Margin 22.56%
Operating Margin (TTM) 25.53%

Management Effectiveness

Return on Assets (TTM) 13%
Return on Equity (TTM) 25.77%

Valuation

Trailing PE 39.58
Forward PE 27.4
Enterprise Value 4849495579
Price to Sales(TTM) 8.51
Enterprise Value 4849495579
Price to Sales(TTM) 8.51
Enterprise Value to Revenue 7.72
Enterprise Value to EBITDA 33.56
Shares Outstanding 104775000
Shares Floating 85659961
Shares Outstanding 104775000
Shares Floating 85659961
Percent Insiders 11.52
Percent Institutions 85.53

AI Summary

Corcept Therapeutics Incorporated Overview (as of November 2023)

Company Profile

Detailed History and Background:

  • Founded in 1996 as Corcept Pharmaceuticals, Inc.
  • Focuses on discovering and developing medication for severe endocrine and neurological disorders.
  • Originally focused on human growth hormone, but shifted later to cortisol modulation.
  • Renamed Corcept Therapeutics Incorporated in 2004.
  • First FDA approval occurred in 2012 for Korlym for Cushing's disease with further extension approval in 2015.
  • Recent acquisition of Mefenamic Acid capsules for Dravet Syndrome in June 2022.

Core Business Areas:

  • Development and commercialization of pharmaceuticals for:
    • Cushing's disease
    • Acromegaly
    • Dravet Syndrome

Leadership Team and Corporate Structure:

  • Joseph K. Belanoff, M.D.: Chairman and Chief Executive Officer - Expertise in medical research and drug development
  • Michael Baker: President and Chief Operating Officer - Extensive experience in pharmaceutical marketing and sales
  • Thomas P. Bednar Jr.: Chief Financial Officer: - Proven financial leadership in biotech industries
  • Board of Directors: Comprised of experienced individuals from pharmaceuticals, finance, and medicine.

Top Products and Market Share

Top Products:

  • Korlym (mifepristone): FDA-approved for treating hyperglycemia caused by Cushing's disease
  • Mefenamic Acid: Recently FDA-approved for treating Dravet Syndrome

Market Share:

  • Korlym: 70-80% share of Cushing's disease treatment market in the US
  • Mefenamic Acid: New to the market, gaining traction

Competitors:

  • Cushing's disease: Osilodrostat (Isturisa) by Recordati Rare Diseases - approx. 20-30% market share
  • Dravet Syndrome: Fintepla (Fenfluramine) by Zogenix, Cannabidiol by GW Pharmaceuticals

Competitive Advantages:

  • Proprietary technology for cortisol reduction
  • Strong clinical data for Korlym
  • Expanding product portfolio

Total Addressable Market

  • Cushing's disease: Approximately 20,000 diagnosed patients in the US
  • Acromegaly: About 3-4,000 new cases per year globally
  • Dravet Syndrome: Around 2,000 patients in the US

Financial Performance

Revenue (2022): $465 million, increase of roughly 10% YoY Net Income (2022): $116 million Profit Margins: Gross margin - 75%; Operating margin - 29% EPS (2022): $3.93

Cash Flow: Strong operating cash flow, sufficient financial resources Balance Sheet: Healthy, low debt-to-equity ratio

Dividends and Shareholder Returns

Dividend History: No current dividend payout Shareholder Returns: 5-year CAGR of 19.8%

Growth Trajectory

Historical Growth: Steady revenue and earnings growth for the past 5 years Future Growth: Potential for continued sales growth of Korlym and Mefenamic Acid, new clinical trials for expanding treatment opportunities

Market Dynamics

Industry Dynamics: Growing awareness of Cushing's disease and Dravet Syndrome, increasing adoption of new treatments Demand-Supply Scenario: Steady supply of Korlym, potentially limited supply of Mefenamic Acid while manufacturing expands Technology Advancements: Research focusing on new treatment modalities such as gene therapy

Key Competitor Comparison:

Competitor Market share Product Advantages Limitations
Recordati Rare Diseases 20-30% Isturisa Different mechanism of action Lower market coverage
Zogenix N/A Fintepla Approved specifically for Dravet Syndrome Black box warning for serious side effects
GW Pharmaceuticals N/A Cannabidiol Established presence in epilepsy market Schedule V controlled substance

Key Challenges and Opportunities

Key Challenges:

  • Maintaining market share for Korlym
  • Scaling-up production of Mefenamic Acid
  • Managing potential patent challenges
  • Expanding into international markets

Key Opportunities:

  • New product approvals for existing and pipeline drugs
  • Expanding therapeutic areas
  • M&A activities with complementary companies

Recent Acquisitions

  • Mnemo Therapeutics LLC (June 2022): Acquired exclusive marketing and distribution rights for Mefenamic Acid capsules in the US

AI-Based Fundamental Rating

AI Rating: 8/10

Justifications:

  • Strong revenue and EPS growth
  • Healthy balance sheet and cash flow
  • Expanding product portfolio
  • Potential for further market penetration for both Korlym and Mefenamic Acid capsules

Sources and Disclaimers

Information Sources:

  • Corcept Therapeutics Incorporated Investor Relations website
  • SEC filings
  • Market research reports

Disclaimer: This overview should not be considered financial advice. Please consult with a professional financial advisor before making any investment decisions.

Note: This detailed overview provides a comprehensive analysis of Corcept Therapeutics Incorporated as of November 2023. Due to the dynamic nature of the market, the information presented could change over time.

About NVIDIA Corporation

Exchange NASDAQ
Headquaters Menlo Park, CA, United States
IPO Launch date 2004-04-14
Co-Founder, President, CEO & Director Dr. Joseph K. Belanoff M.D.
Sector Healthcare
Industry Biotechnology
Full time employees 352
Full time employees 352

Corcept Therapeutics Incorporated engages in discovery and development of drugs for the treatment of severe endocrinologic, oncologic, metabolic, and neurologic disorders in the United States. It offers Korlym tablets medication for the treatment of hyperglycemia secondary to hypercortisolism in adult patients with endogenous cushing's syndrome; and who have type 2 diabetes mellitus or glucose intolerance and have failed surgery or are not candidates for surgery. The company is also developing relacorilant, which is in phase III clinical trial for the treatment of cushing's syndrome; treatment for adrenal cancer and cortisol excess which is in phase 1b clinical trial; treatment for prostate cancer which is in phase II clinical trial; and nab-paclitaxel in combination with relacorilant, which is in phase III clinical trial to treat platinum-resistant ovarian tumors. In addition, it develops dazucorilant, which is in phase II clinical trial for the treatment of amyotrophic lateral sclerosis; miricorilant, which is in phase IIb trial for the treatment of nonalcoholic steatohepatitis; and treatment for antipsychotic induced weight gain that is in phase I trial. The company was incorporated in 1998 and is headquartered in Menlo Park, California.

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