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HCM Overview

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Intellectia

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High
11.270
Open
11.190
VWAP
11.13
Vol
56.21K
Mkt Cap
2.03B
Low
11.040
Amount
625.58K
EV/EBITDA(TTM)
--
Total Shares
174.47M
EV
792.71M
EV/OCF(TTM)
--
P/S(TTM)
3.74
HUTCHMED (China) Ltd is an investment holding company principally engaged in the manufacture and sale of pharmaceuticals. The Company operates its business through two segments. Oncology Immunology segment is engaged in the discovery, development and commercialization of targeted therapies and immunotherapies for the treatment of cancer and immunological diseases. Among it, research and development (R&D) includes research and development activities covering drug discovery, development, manufacturing and regulatory functions, out-licensing of in-house developed drugs, as well as administrative activities to support research and development operations, marketed products comprises the invoiced sales, marketing, manufacture and distribution of drugs developed from research and development activities. Other Ventures segment is engaged in the other commercial businesses which include the sales, marketing, manufacture and distribution of other prescription drugs and healthcare products.
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Events Timeline

(ET)
2026-07-02
05:30:00
Hutchmed's Orpathys Receives Conditional Approval from NMPA
select
2026-05-21 (ET)
2026-05-21
06:10:00
Innovent Biologics and Hutchmed Announce New Drug Approval
select
2026-05-21
06:10:00
Hutchmed and Innovent Biologics Announce New Drug Application Approval
select
2026-04-29 (ET)
2026-04-29
06:30:00
Hutchmed's Sovleplenib New Drug Application Accepted for Priority Review
select
2026-03-09 (ET)
2026-03-09
05:40:00
Hutchmed Announces Withdrawal of Tazverik in China
select
2026-01-14 (ET)
2026-01-14
05:40:00
Hutchmed Reports SACHI Phase III Trial Results
select

News

Newsfilter
9.0
07-02Newsfilter
HUTCHMED Receives Conditional Approval for ORPATHYS® in Gastric Cancer
  • NDA Approval: HUTCHMED's ORPATHYS® (savolitinib) has received conditional approval from the China National Medical Products Administration for treating MET-amplified advanced gastric cancer patients, marking a significant advancement in precision medicine.
  • Clinical Trial Results: In a pivotal Phase II registration study, ORPATHYS® achieved an objective response rate (ORR) of 32.3%, exceeding the pre-specified efficacy threshold, indicating its potential to significantly improve patient outcomes in MET-amplified gastric cancer.
  • Market Demand: With MET amplification accounting for approximately 4-6% of gastric cancer patients and an estimated annual incidence of 18,000 in China, the approval of ORPATHYS® provides a new treatment option for this high-demand market, further solidifying HUTCHMED's market position.
  • Strategic Partnership: HUTCHMED's collaboration with AstraZeneca will accelerate the commercialization of ORPATHYS®, expected to enhance its availability in the Chinese market and meet the growing needs of cancer patients.
Newsfilter
9.5
06-30Newsfilter
HUTCHMED to Announce Interim Results on July 30
  • Interim Results Announcement: HUTCHMED will announce its interim results for the six months ended June 30, 2026, on July 30, 2026, at 7:00 am EDT, showcasing the company's latest advancements in the biopharmaceutical sector.
  • Webcast Presentation: Management will host an English webcast at 8:00 am EDT on the same day, followed by a Q&A session, aimed at enhancing interaction with analysts and investors.
  • Chinese Webcast Timing: The Chinese (Putonghua) webcast is scheduled for 8:30 am HKT on July 31, 2026, further broadening communication channels with Mandarin-speaking investors.
  • Company Background: HUTCHMED is an innovative commercial-stage biopharmaceutical company focused on the discovery, development, and commercialization of targeted therapies and immunotherapies for cancer and immunological diseases, committed to bringing drug candidates from in-house discovery to patients worldwide.
NASDAQ.COM
8.5
06-25NASDAQ.COM
HUTCHMED's Fanregratinib Meets Primary Endpoint in Phase 2 Study
  • Clinical Trial Success: HUTCHMED's Fanregratinib achieved a 42.5% objective response rate in the pivotal Phase 2 registrational study for intrahepatic cholangiocarcinoma, successfully meeting its primary endpoint and demonstrating potential in treating advanced patients.
  • Drug Application Progress: The New Drug Application for Fanregratinib has been accepted for priority review by the Chinese National Medical Products Administration in December 2025, based on Phase 2 trial data, accelerating its path to commercialization.
  • Safety Assessment: Among treated patients, 48.3% reported drug-related adverse events of Grade 3 or higher, primarily elevated liver enzymes and palmar-plantar erythrodysesthesia syndrome, indicating a safety profile consistent with known FGFR inhibitor mechanisms.
  • Future Presentation Plans: The trial results will be presented at the European Society for Medical Oncology Gastrointestinal Cancers Congress on July 4, 2024, in Munich, Germany, which is expected to further enhance Fanregratinib's market visibility and clinical recognition.
Newsfilter
9.0
06-25Newsfilter
Fanregratinib Shows Promising Results in ICC Treatment
  • Clinical Trial Results: Fanregratinib achieved an objective response rate of 42.5% in a pivotal Phase II registration study for advanced intrahepatic cholangiocarcinoma (ICC) patients with FGFR2 fusions/rearrangements, highlighting its potential as a new treatment option, particularly for those previously treated with chemotherapy.
  • Survival Data: The study reported a median overall survival of 16.6 months with no treatment-related deaths, indicating significant clinical value in improving patient survival rates and the potential to reshape treatment paradigms in this challenging patient population.
  • Safety Profile: While 48.3% of patients experienced drug-related adverse events of Grade 3 or higher, the treatment discontinuation rate was only 2.2%, demonstrating a favorable safety profile for Fanregratinib, making it suitable for broader clinical application.
  • Regulatory Progress: The New Drug Application (NDA) for Fanregratinib has been accepted for priority review by the China National Medical Products Administration, marking a significant step towards its potential market launch in China and enhancing HUTCHMED's competitive position in the global biopharmaceutical landscape.
NASDAQ.COM
9.0
06-12NASDAQ.COM
HUTCHMED Reports Phase III Results for Sovleplenib in wAIHA
  • Clinical Trial Success: HUTCHMED's Sovleplenib demonstrated a durable response rate of 66% in the Phase III ESLIM-02 study, significantly higher than the 15% in the placebo group, indicating strong efficacy in treating wAIHA and potentially enhancing market acceptance.
  • Significant Market Potential: The market for wAIHA is projected to grow from $0.6 billion in 2025 to $0.93 billion by 2030, with a CAGR of 9.2%, providing a robust commercial foundation for Sovleplenib's market entry.
  • Favorable Safety Profile: Sovleplenib exhibited a favorable safety profile, with 43% of patients experiencing grade 3 or higher treatment-emergent adverse events compared to 59% in the placebo group, indicating a competitive edge in safety.
  • Rapid Response Time: The median time to response for Sovleplenib was 3.1 weeks, significantly shorter than the 6.3 weeks for placebo, with longer response duration, highlighting its potential advantages in clinical application and attracting investor interest.
Newsfilter
9.0
06-12Newsfilter
Sovleplenib Shows Promising Results in wAIHA Treatment
  • Clinical Trial Results: The ESLIM-02 study demonstrated that sovleplenib achieved a durable response rate of 66% in 90 treated patients, significantly surpassing the 15% in the placebo group (p<0.0001), indicating its substantial potential in treating wAIHA.
  • Safety Profile: Sovleplenib exhibited a favorable safety profile with grade ≥3 adverse events occurring in 43% of patients, lower than the 59% in the placebo group, and no treatment-related deaths or discontinuations reported, highlighting its viability for clinical use.
  • Significant Treatment Effects: During the 24-week double-blind treatment period, sovleplenib significantly reduced the proportion of patients requiring rescue therapy (16% vs 54%, p=0.0001), with 50% of patients able to taper or discontinue glucocorticoids, thereby enhancing patient quality of life.
  • Regulatory Progress: Sovleplenib has received priority review from the China National Medical Products Administration and accepted a New Drug Application in April 2026, marking significant regulatory advancements in the treatment landscape for wAIHA and indicating potential market opportunities ahead.
Wall Street analysts forecast HCM stock price to rise
1 Analyst Rating
Wall Street analysts forecast HCM stock price to rise
1 Buy
0 Hold
0 Sell
Moderate Buy
Current: 0.000
sliders
Low
22.00
Averages
22.00
High
22.00
Current: 0.000
sliders
Low
22.00
Averages
22.00
High
22.00
BofA
Alec Stranahan
Buy
downgrade
$20 -> $17
AI Analysis
2026-07-07
New
Reason
BofA
Alec Stranahan
Price Target
$20 -> $17
AI Analysis
2026-07-07
New
downgrade
Buy
Reason
BofA analyst Alec Stranahan lowered the firm's price target on Hutchmed to $17 from $20 and keeps a Buy rating on the shares. The print will likely refocus attention on whether the commercial rebound exiting 2025 is sustainable, with fruquintinib representing the key swing factor, the analyst tells investors in a research note.
Morgan Stanley
Underweight -> Equal Weight
upgrade
2026-05-28
Reason
Morgan Stanley
Price Target
2026-05-28
upgrade
Underweight -> Equal Weight
Reason
Morgan Stanley upgraded Hutchmed to Equal Weight from Underweight with a price target of $13.60, down from $13.75. The valuation of China biotech stocks has \"reset to a better entry point\" while FY26 guidance \"still implies robust innovator topline growth\" and outbound licensing momentum remains strong, the analyst tells investors in a note on the group.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for HCM
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Valuation Metrics

The current forward P/E ratio for HUTCHMED (China) Ltd (HCM.O) is 13.09, compared to its 5-year average forward P/E of 20.31. For a more detailed relative valuation and DCF analysis to assess HUTCHMED (China) Ltd's fair value, Click here.

Forward PE

The forward P/E ratio is a valuation metric that divides a company's current stock price by its estimated future earnings per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average PE
20.31
Current PE
13.09
Overvalued PE
326.69
Undervalued PE
-286.07

Forward EV/EBITDA

The forward EV/EBITDA ratio is a valuation metric that divides a company's enterprise value (EV) by its estimated future earnings before interest, taxes, depreciation, and amortization (EBITDA) over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
N/A
5Y Average EV/EBITDA
-85.04
Current EV/EBITDA
-23.70
Overvalued EV/EBITDA
70.54
Undervalued EV/EBITDA
-240.62

Forward PS

The forward P/S ratio is a valuation metric that divides a company's current stock price by its estimated future sales (or revenue) per share over the next 12 months.
StronglyUndervaluedUndervaluedFairOvervaluedStronglyOvervalueddotted line Image
5Y Average PS
5.25
Current PS
2.69
Overvalued PS
8.98
Undervalued PS
1.51

Financials

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Whales Holding HCM

A
AEGON-Industrial Fund Management Co. Ltd.
Holding
HCM
-18.69%
3M Return

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Frequently Asked Questions

What is HUTCHMED (China) Ltd (HCM) stock price today?

The current price of HCM is 11.08 USD — it has decreased -4.89

What is HUTCHMED (China) Ltd (HCM)'s business?

HUTCHMED (China) Ltd is an investment holding company principally engaged in the manufacture and sale of pharmaceuticals. The Company operates its business through two segments. Oncology Immunology segment is engaged in the discovery, development and commercialization of targeted therapies and immunotherapies for the treatment of cancer and immunological diseases. Among it, research and development (R&D) includes research and development activities covering drug discovery, development, manufacturing and regulatory functions, out-licensing of in-house developed drugs, as well as administrative activities to support research and development operations, marketed products comprises the invoiced sales, marketing, manufacture and distribution of drugs developed from research and development activities. Other Ventures segment is engaged in the other commercial businesses which include the sales, marketing, manufacture and distribution of other prescription drugs and healthcare products.

What is the price predicton of HCM Stock?

Wall Street analysts forecast HCM stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for HCM is22.00 USD with a low forecast of 22.00 USD and a high forecast of 22.00 USD. However, analyst price targets are subjective and often lag stock prices, so investors should focus on the objective reasons behind analyst rating changes, which better reflect the company's fundamentals.

What is HUTCHMED (China) Ltd (HCM)'s revenue for the last quarter?

HUTCHMED (China) Ltd revenue for the last quarter amounts to NaN USD, decreased

What is HUTCHMED (China) Ltd (HCM)'s earnings per share (EPS) for the last quarter?

HUTCHMED (China) Ltd. EPS for the last quarter amounts to USD, decreased

How many employees does HUTCHMED (China) Ltd (HCM). have?

HUTCHMED (China) Ltd (HCM) has 1796 emplpoyees as of July 07 2026.

What is HUTCHMED (China) Ltd (HCM) market cap?

Today HCM has the market capitalization of 2.03B USD.