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INCY Overview

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$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
$
0.000
0.000(0.000%)
At close
0.000(0.000%)Aft-market
ET
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Intellectia

Loading chart...

High
99.620
Open
99.580
VWAP
97.98
Vol
4.06M
Mkt Cap
19.62B
Low
96.090
Amount
397.65M
EV/EBITDA(TTM)
10.12
Total Shares
199.78M
EV
15.64B
EV/OCF(TTM)
10.31
P/S(TTM)
3.72
Incyte Corporation is a biopharmaceutical company, which is engaged in the discovery, development, and commercialization of therapeutics. The Company operates in three therapeutic areas: Hematology, Oncology, and Inflammation and Autoimmunity (IAI). Its hematology franchise includes four approved products, JAKAFI (ruxolitinib), ICLUSIG (ponatinib), MONJUVI (tafasitamab-cxix)/MINJUVI (tafasitamab) and NIKTIMVO (axatilimab-csfr), as well as multiple clinical development programs. Its oncology franchise includes two approved products, PEMAZYRE (pemigatinib) and ZYNYZ (retifanlimab-dlwr), as well as several clinical development programs. Its Inflammation and Autoimmunity franchise is comprised of one approved product, OPZELURA (ruxolitinib) cream, with several clinical programs in development. The Company manages business activities on a consolidated basis through the development and commercialization of oncology and dermatology products.
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Events Timeline

(ET)
2026-06-19
07:30:00
Incyte Japan Receives Approval for Minjuvi Combination Therapy for Large B-Cell Lymphoma
select
2026-06-14 (ET)
2026-06-14
17:30:00
Incyte Updates Clinical Data on INCA033989
select
2026-06-14
17:30:00
Incyte Reports Positive Phase 3 Results for Tafasitamab
select
2026-06-14
17:30:00
Mirum and Incyte Announce Phase 2 Results for Zilurgisertib
select
2026-06-04 (ET)
2026-06-04
08:10:00
Mirum and Incyte to Present Zilurgisertib Study Results at ENDO 2026
select
2026-05-31 (ET)
2026-05-31
09:30:00
Incyte Reports Positive Phase 3 Trial Results for Tafasitamab
select

News

Newsfilter
8.5
06-19Newsfilter
PinnedJapan Approves Minjuvi for Lymphoma Treatment
  • New Treatment Approval: Japan's Ministry of Health, Labour and Welfare has approved Minjuvi® (tafasitamab) in combination with lenalidomide for treating relapsed or refractory diffuse large B-cell lymphoma (DLBCL), providing a new option for patients, particularly those ineligible for autologous stem cell transplant.
  • Clinical Trial Results: The L-MIND trial demonstrated an overall response rate of 58.8% for Minjuvi combined with lenalidomide, with a complete response rate of 41.3% and a partial response rate of 17.5%, while the J-MIND trial reported an even higher response rate of 71.4%, indicating the efficacy of this combination.
  • Safety Assessment: Although the main adverse events included neutropenia and thrombocytopenia, the overall safety profile of Minjuvi in combination with lenalidomide was manageable, suggesting its clinical applicability.
  • Market Outlook: This approval marks the second regulatory endorsement for Minjuvi in Japan, highlighting Incyte's commitment to addressing critical unmet needs and is expected to drive further growth in the Japanese market.
NASDAQ.COM
9.0
06-19NASDAQ.COM
Incyte's Minjuvi Approved in Japan for DLBCL Treatment
  • Drug Approval: Incyte Biosciences announced that Japan's Ministry of Health, Labour and Welfare has approved Minjuvi (tafasitamab) in combination with lenalidomide for treating relapsed or refractory diffuse large B-cell lymphoma (DLBCL), providing new treatment options for patients.
  • Clinical Trial Support: This approval is supported by data from the global Phase II L-MIND study and Japan's Phase Ib/II J-MIND trial, which demonstrated strong response rates and durable clinical benefits in patients ineligible for autologous stem cell transplant.
  • Safety Profile: The combination therapy maintained a manageable safety profile, with common side effects including neutropenia and thrombocytopenia, indicating its acceptability in treatment regimens.
  • Market Impact: This marks Minjuvi's second approval in Japan, following its earlier authorization for relapsed or refractory follicular lymphoma, thereby expanding treatment options for this aggressive blood cancer.
NASDAQ.COM
6.5
06-19NASDAQ.COM
Zacks Premium Empowers Investors with Confidence and Insights
  • Investor Confidence Boost: Zacks Premium offers daily updates on Zacks Rank and Industry Rank, aiding investors in making more informed decisions, thereby enhancing investment confidence and optimizing portfolios.
  • Style Scoring System: The Zacks Style Scores rate stocks from A to F based on value, growth, and momentum characteristics, helping investors identify stocks with the potential to outperform the market over the next 30 days, thus enhancing the scientific approach to investing.
  • Strong Earnings Outlook: Incyte Corporation (INCY) holds a Zacks Rank of #3 and a VGM Score of A, with a 0.8% increase in share price over the past four weeks, indicating its momentum appeal in the medical sector, attracting more investor attention.
  • Expert Stock Recommendations: Five Zacks experts have each selected a stock expected to rise over 100% in the coming months, further boosting investor confidence in potential high-return stocks, especially in the current market environment.
NASDAQ.COM
9.0
06-17NASDAQ.COM
Mirum and Incyte Report Positive Results for FOP Study
  • Clinical Trial Results: Mirum and Incyte's Phase II PROGRESS study of zilurgisertib showed that only 3.1% of patients developed new lesions compared to 16.7% in the placebo group, achieving an 81% reduction, indicating the drug's potential in treating this ultra-rare disease.
  • Sustained Efficacy: In the open-label extension phase, no new lesions were observed among patients continuing zilurgisertib treatment at 48 weeks, with total lesion volume continuing to decline, demonstrating the drug's long-term efficacy and safety, addressing the urgent need for effective treatments.
  • FDA Priority Review: Following positive clinical data, the FDA has accepted the NDA for zilurgisertib and granted Priority Review status, with a decision expected by September 26, 2026, which will expedite the drug's market entry to meet the demand for new therapies.
  • Market Performance: Year-to-date, shares of Mirum and Incyte have risen by 28.5% and 1%, respectively, against a 1.4% decline in the biotech sector, reflecting investor optimism regarding their clinical advancements and enhancing their competitive position in the market.
seekingalpha
9.0
06-15seekingalpha
Mirum and Incyte Report Positive Phase 2 Data for Zilurgisertib
  • Clinical Trial Results: Mirum Pharmaceuticals and Incyte have reported positive pivotal Phase 2 data for their oral FOP candidate, zilurgisertib, with results from Cohort 1 of the PROGRESS study showing consistent treatment effects on disease activity and durability through Week 48, indicating the drug's therapeutic potential.
  • Safety Assessment: During the open-label extension, no new HO lesions were observed in patients continuing zilurgisertib treatment or in placebo patients who crossed over to active treatment at week 24, demonstrating the drug's safety and efficacy in long-term use.
  • FDA Review Progress: The U.S. Food and Drug Administration (FDA) has accepted the New Drug Application for zilurgisertib and granted Priority Review, with a target action date set for September 26, 2026, laying the groundwork for the drug's market launch.
  • Market Outlook: Incyte's Chief Medical Officer Steven Stein stated that the findings represent an important milestone for the zilurgisertib program, further strengthening the clinical evidence supporting its potential as a treatment for FOP, signaling future market opportunities in the rare disease sector.
Yahoo Finance
8.5
06-14Yahoo Finance
Mirum and Incyte Announce New Progress in FOP Treatment
  • Clinical Trial Results: At the ENDO 2026 conference, Mirum and Incyte presented results from Cohort 1 of the PROGRESS study, showing an 81% reduction in new heterotopic ossification lesions in patients treated with zilurgisertib, indicating significant efficacy in treating FOP.
  • FDA Priority Review: The U.S. FDA has accepted the New Drug Application for zilurgisertib and granted Priority Review, with a decision expected by September 26, 2026, which could provide urgently needed treatment options for FOP patients and potentially reshape the market landscape.
  • Patient Data Analysis: During the 24-week double-blind period, patients receiving zilurgisertib had significantly fewer new lesions compared to the placebo group, and no new lesions were observed during the 48-week open-label extension, demonstrating sustained treatment effects and enhancing the drug's market potential.
  • Safety Assessment: The study indicated that zilurgisertib was well-tolerated during the 24-week controlled period, with most adverse events being mild or moderate and no treatment discontinuations, paving the way for future commercialization and boosting investor confidence.
Wall Street analysts forecast INCY stock price to rise
19 Analyst Rating
Wall Street analysts forecast INCY stock price to rise
9 Buy
9 Hold
1 Sell
Moderate Buy
Current: 0.000
sliders
Low
73.00
Averages
100.31
High
125.00
Current: 0.000
sliders
Low
73.00
Averages
100.31
High
125.00
Stifel
Buy
maintain
$120 -> $123
AI Analysis
2026-04-29
Reason
Stifel
Price Target
$120 -> $123
AI Analysis
2026-04-29
maintain
Buy
Reason
Stifel raised the firm's price target on Incyte to $123 from $120 and keeps a Buy rating on the shares.
Oppenheimer
Perform
maintain
$84 -> $90
2026-04-29
Reason
Oppenheimer
Price Target
$84 -> $90
2026-04-29
maintain
Perform
Reason
Oppenheimer raised the firm's price target on Incyte to $90 from $84 and keeps a Perform rating on the shares. The firm notes the company reported Q1 results boasting both top-line and bottom-line beats, while FY26 guidance of was maintained. Generally, Oppenheimer sees Incyte's updates as relatively straightforward while it sees focus shifting to clinical readouts expected this year, specifically in oncology.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for INCY
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Valuation Metrics

The current forward P/E ratio for Incyte Corp (INCY.O) is 12.76, compared to its 5-year average forward P/E of 18.03. For a more detailed relative valuation and DCF analysis to assess Incyte Corp'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
5Y Average PE
18.03
Current PE
12.76
Overvalued PE
25.62
Undervalued PE
10.44

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
5Y Average EV/EBITDA
13.14
Current EV/EBITDA
9.55
Overvalued EV/EBITDA
18.53
Undervalued EV/EBITDA
7.76

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
3.78
Current PS
3.13
Overvalued PS
4.66
Undervalued PS
2.90

Financials

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A
Applied Finance Advisors, LLC
Holding
INCY
+25.77%
3M Return
A
Avoro Capital Advisors LLC
Holding
INCY
+24.79%
3M Return
R
Renaissance Technologies Corp.
Holding
INCY
+18.99%
3M Return
A
AQR Capital Management
Holding
INCY
+17.05%
3M Return
A
Armistice Capital LLC
Holding
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+17.03%
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Arax Advisory Partners, LLC
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+16.43%
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Frequently Asked Questions

What is Incyte Corp (INCY) stock price today?

The current price of INCY is 98.22 USD — it has decreased -0.78

What is Incyte Corp (INCY)'s business?

Incyte Corporation is a biopharmaceutical company, which is engaged in the discovery, development, and commercialization of therapeutics. The Company operates in three therapeutic areas: Hematology, Oncology, and Inflammation and Autoimmunity (IAI). Its hematology franchise includes four approved products, JAKAFI (ruxolitinib), ICLUSIG (ponatinib), MONJUVI (tafasitamab-cxix)/MINJUVI (tafasitamab) and NIKTIMVO (axatilimab-csfr), as well as multiple clinical development programs. Its oncology franchise includes two approved products, PEMAZYRE (pemigatinib) and ZYNYZ (retifanlimab-dlwr), as well as several clinical development programs. Its Inflammation and Autoimmunity franchise is comprised of one approved product, OPZELURA (ruxolitinib) cream, with several clinical programs in development. The Company manages business activities on a consolidated basis through the development and commercialization of oncology and dermatology products.

What is the price predicton of INCY Stock?

Wall Street analysts forecast INCY stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for INCY is100.31 USD with a low forecast of 73.00 USD and a high forecast of 125.00 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 Incyte Corp (INCY)'s revenue for the last quarter?

Incyte Corp revenue for the last quarter amounts to 1.27B USD, increased 20.87

What is Incyte Corp (INCY)'s earnings per share (EPS) for the last quarter?

Incyte Corp. EPS for the last quarter amounts to 1.47 USD, increased 83.75

How many employees does Incyte Corp (INCY). have?

Incyte Corp (INCY) has 2844 emplpoyees as of June 20 2026.

What is Incyte Corp (INCY) market cap?

Today INCY has the market capitalization of 19.62B USD.