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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
94.420
Open
91.540
VWAP
93.24
Vol
1.83M
Mkt Cap
18.73B
Low
91.170
Amount
170.29M
EV/EBITDA(TTM)
10.05
Total Shares
199.01M
EV
14.43B
EV/OCF(TTM)
10.21
P/S(TTM)
3.53
Incyte Corporation is a biopharmaceutical company, which is focused on the discovery, development, and commercialization of therapeutics. The Company operates in two therapeutic areas. One therapeutic area is Hematology/Oncology, which is comprised of Myeloproliferative Neoplasms and Graft-Versus-Host Disease, as well as solid tumors and hematologic malignancies. Its other therapeutic area is Inflammation and Autoimmunity, which includes its Dermatology commercial franchise. Its hematology and oncology franchise are comprised of six products, which are JAKAFI (ruxolitinib), MONJUVI (tafasitamab-cxix)/MINJUVI (tafasitamab), PEMAZYRE (pemigatinib), ICLUSIG (ponatinib), NIKTIMVO (axatilimab-csfr), and ZYNYZ (retifanlimab-dlwr), as well as numerous clinical development programs. The Company's pipeline also includes two first-in-class small molecule antagonist of Mas-related G protein-coupled receptor (MRGPRX2) and INCB000547, an oral MRGPRX4 antagonist.
Show More

Events Timeline

(ET)
2026-03-29
11:00:00
Incyte Releases 54-Week Clinical Data for Povorcitinib
select
2026-03-25 (ET)
2026-03-25
09:10:00
Incyte Appoints New Executives to Support Strategic Growth
select
2026-03-17 (ET)
2026-03-17
07:40:00
Knight Therapeutics Submits New Indication Application for MINJUVI
select
2026-03-06 (ET)
2026-03-06
16:50:00
Incyte's Zynyz Approved by EU for Metastatic Anal Canal SCC Treatment
select
2026-02-27 (ET)
2026-02-27
08:20:00
Eli Lilly and Incyte Announce Positive EMA Opinion for Olumiant
select
2026-02-18 (ET)
2026-02-18
07:40:00
Knight Therapeutics Submits NIKTIMVO Marketing Application in Brazil
select

News

Newsfilter
8.5
03-28Newsfilter
Povorcitinib Shows Significant Efficacy in Hidradenitis Suppurativa Treatment
  • Significant Clinical Efficacy: The 54-week data from the STOP-HS program demonstrated that 71.4% of patients achieved HiSCR50 with povorcitinib, indicating substantial long-term efficacy in moderate to severe hidradenitis suppurativa (HS) patients, potentially transforming treatment paradigms.
  • Good Safety Profile: The safety data over 54 weeks showed that treatment-emergent adverse events (TEAEs) occurred in 76.2% to 83.4% of patients, mostly mild to moderate, indicating a favorable tolerance for povorcitinib.
  • Quality of Life Improvements: At Week 54, 40.5% to 46.8% of patients reported significant improvements in skin pain, and 49.0% to 58.0% experienced reductions in fatigue, suggesting that povorcitinib not only alleviates pathological symptoms but also enhances overall quality of life.
  • Regulatory Application Progress: The STOP-HS data support the New Drug Application (NDA) and Marketing Authorization Application (MAA) for povorcitinib, which are currently under review by the U.S. FDA and European Medicines Agency, indicating its potential as the first oral treatment option for HS patients.
Yahoo Finance
8.5
03-28Yahoo Finance
Povorcitinib Shows Significant Efficacy in HS Treatment at 54 Weeks
  • Significant Clinical Efficacy: The 54-week data from the STOP-HS program show that 71.4% of patients achieved HiSCR50, indicating povorcitinib's long-term efficacy in moderate to severe hidradenitis suppurativa (HS) patients, potentially transforming treatment paradigms.
  • Notable Symptom Improvement: Post-treatment, 40.5% to 46.8% of patients reported significant reductions in skin pain, while 49.0% to 58.0% experienced less fatigue, highlighting povorcitinib's positive impact on quality of life.
  • Good Safety Profile: Povorcitinib's safety over 54 weeks aligns with previous 24-week data, with 76.2% to 83.4% of patients experiencing treatment-emergent adverse events, mostly mild to moderate, and serious adverse events occurring at rates below 6.4%.
  • Regulatory Application Progress: The STOP-HS data support the NDA and MAA submissions for povorcitinib, currently under review by the U.S. FDA and European EMA, indicating its potential as an oral treatment option.
moomoo
9.0
03-28moomoo
INCYTE: PHASE 3 RESULTS FROM STOP-HS TRIAL DEMONSTRATE SUSTAINED CLINICAL EFFICACY OF POVORCITINIB THROUGH WEEK 54 IN MODERATE TO SEVERE HS PATIENTS
  • Phase 3 Data: Recent Phase 3 data from the STOP-HSV program indicates significant clinical efficacy in treating patients with moderate to severe herpes simplex virus (HSV) infections.

  • Durable Efficacy: The findings demonstrate that the treatment maintains durable clinical efficacy through week 54, suggesting long-term benefits for patients.

  • Patient Population: The study focused on patients experiencing moderate to severe HSV symptoms, highlighting the program's relevance to those most affected by the virus.

  • Implications for Treatment: These results may influence future treatment protocols and provide new options for managing HSV infections effectively.

Newsfilter
9.0
03-20Newsfilter
Incyte Unveils Latest Data on Povorcitinib at AAD 2026
  • Clinical Data Presentation: Incyte will present 54-week efficacy and safety data for povorcitinib in hidradenitis suppurativa patients at the 2026 AAD Annual Meeting, further validating its growth potential in the inflammation and autoimmunity sector.
  • Diverse Research Showcase: The conference will feature multiple ePosters for ruxolitinib cream and povorcitinib, covering atopic dermatitis, hidradenitis suppurativa, and vitiligo, highlighting Incyte's extensive research footprint in dermatological treatments.
  • Promising Market Outlook: As an oral small-molecule JAK1 selective inhibitor, povorcitinib is undergoing Phase 3 trials for hidradenitis suppurativa, vitiligo, and prurigo nodularis, which are expected to create significant market opportunities for the company.
  • Innovative Drug Approval: Opzelura® (ruxolitinib cream) has been approved by the FDA for the topical treatment of non-segmental vitiligo, becoming the first approved repigmentation treatment in the U.S., further solidifying Incyte's leadership in the dermatology market.
Globenewswire
8.5
03-17Globenewswire
Knight Therapeutics Secures New Drug Approval in Brazil
  • New Indication Approved: Knight Therapeutics' Brazilian affiliate, United Medical Ltda., received ANVISA approval for MINJUVI® in combination with rituximab and lenalidomide for relapsed or refractory follicular lymphoma, marking a significant expansion in treatment options that is expected to greatly improve patient outcomes.
  • Clinical Data Support: The approval is backed by clinical study data demonstrating meaningful response rates and durable disease control with MINJUVI® combined with R2, which is anticipated to enhance Knight's competitiveness in the Latin American market and meet the growing treatment demand.
  • Strengthened Strategic Partnership: Knight entered into an exclusive supply and distribution agreement with Incyte in 2021, further solidifying its position in the Latin American market, with expectations that the promotion of MINJUVI® will increase market share and enhance the company's influence in oncology treatment.
  • Positive Future Outlook: This approval not only provides Brazilian patients with a new treatment option but also showcases Knight's strong capabilities in rapid approval processes, which is expected to drive business growth in Latin America and further fulfill its commitment to high-quality cancer care.
Globenewswire
8.5
03-17Globenewswire
Knight Therapeutics Submits MINJUVI Supplemental Application for New Indication
  • New Indication Application: Knight Therapeutics' Argentine and Mexican affiliates have submitted a supplemental application for MINJUVI® (tafasitamab) to local regulatory agencies, aiming to expand the product's applicability in the Latin American market and enhance its competitive edge.
  • Market Expansion Strategy: Since signing an exclusive supply agreement with Incyte in 2021, Knight has launched MINJUVI® in Brazil, Mexico, and Argentina, planning to leverage the new indication approval to meet diverse patient needs, thereby increasing sales potential and market share.
  • Clinical Data Support: In a Phase 3 clinical trial for relapsed follicular lymphoma, MINJUVI® demonstrated a significant improvement in progression-free survival, reaching 22.37 months, indicating the drug's efficacy in treatment, which may attract more physician interest.
  • Future Development Outlook: Knight Therapeutics CEO Samira Sakhia emphasized that MINJUVI® represents multiple therapies rather than a single product, and with the launch of new indications, the company will continue to focus on improving patient health and driving long-term growth in the Latin American market.
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
UBS
Neutral
to
Hold
downgrade
$104 -> $94
AI Analysis
2026-03-25
Reason
UBS
Price Target
$104 -> $94
AI Analysis
2026-03-25
downgrade
Neutral
to
Hold
Reason
UBS lowered the firm's price target on Incyte to $94 from $104 and keeps a Neutral rating on the shares.
Jefferies
Faisal Khurshid
Buy
to
Hold
downgrade
$120 -> $94
2026-03-16
Reason
Jefferies
Faisal Khurshid
Price Target
$120 -> $94
2026-03-16
downgrade
Buy
to
Hold
Reason
Jefferies analyst Faisal Khurshid downgraded Incyte to Hold from Buy with a price target of $94, down from $120, after assuming coverage of the name. The firm cites patent cliff concerns for the downgrade. The Jakafi loss of exclusivity in 2028 is an "existential event" for Incyte, and Jefferies does not see a growth outlook that justifies upside from current share levels, the analyst tells investors in a research note. The firm says the company's biggest value drivers are "years away and/or hard to underwrite."
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 13.67, compared to its 5-year average forward P/E of 18.83. 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
18.83
Current PE
13.67
Overvalued PE
26.55
Undervalued PE
11.11

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
13.91
Current EV/EBITDA
9.44
Overvalued EV/EBITDA
19.42
Undervalued EV/EBITDA
8.40

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
3.95
Current PS
3.70
Overvalued PS
4.95
Undervalued PS
2.95

Financials

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Whales Holding INCY

A
Avoro Capital Advisors LLC
Holding
INCY
+5.71%
3M Return
L
LSV Asset Management
Holding
INCY
+1.57%
3M Return
B
Baker Bros. Advisors LP
Holding
INCY
+1.44%
3M Return
A
Andra AP-fonden
Holding
INCY
+1.27%
3M Return
A
Arax Advisory Partners, LLC
Holding
INCY
+0.21%
3M Return
S
Sound Shore Management, Inc.
Holding
INCY
-1.14%
3M Return

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Frequently Asked Questions

What is Incyte Corp (INCY) stock price today?

The current price of INCY is 94.12 USD — it has increased 4.2

What is Incyte Corp (INCY)'s business?

Incyte Corporation is a biopharmaceutical company, which is focused on the discovery, development, and commercialization of therapeutics. The Company operates in two therapeutic areas. One therapeutic area is Hematology/Oncology, which is comprised of Myeloproliferative Neoplasms and Graft-Versus-Host Disease, as well as solid tumors and hematologic malignancies. Its other therapeutic area is Inflammation and Autoimmunity, which includes its Dermatology commercial franchise. Its hematology and oncology franchise are comprised of six products, which are JAKAFI (ruxolitinib), MONJUVI (tafasitamab-cxix)/MINJUVI (tafasitamab), PEMAZYRE (pemigatinib), ICLUSIG (ponatinib), NIKTIMVO (axatilimab-csfr), and ZYNYZ (retifanlimab-dlwr), as well as numerous clinical development programs. The Company's pipeline also includes two first-in-class small molecule antagonist of Mas-related G protein-coupled receptor (MRGPRX2) and INCB000547, an oral MRGPRX4 antagonist.

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 1.51B USD, increased 27.84

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

Incyte Corp. EPS for the last quarter amounts to 1.46 USD, increased 50.52

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

Incyte Corp (INCY) has 2844 emplpoyees as of April 01 2026.

What is Incyte Corp (INCY) market cap?

Today INCY has the market capitalization of 18.73B USD.