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BIIB 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
195.200
Open
189.680
VWAP
192.72
Vol
931.58K
Mkt Cap
28.56B
Low
189.500
Amount
179.53M
EV/EBITDA(TTM)
8.88
Total Shares
147.64M
EV
30.57B
EV/OCF(TTM)
11.80
P/S(TTM)
2.87
Biogen Inc. is a global biopharmaceutical company. The Company is focused on discovering, developing, and delivering advanced therapies for people living with serious and complex diseases worldwide. It operates a portfolio of medicines to treat multiple sclerosis (MS), spinal muscular atrophy (SMA), Alzheimer's disease, and amyotrophic lateral sclerosis (ALS). It is focused on advancing its pipeline in neurology, specialized immunology, and rare diseases. Its marketed products include TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, TYSABRI and FAMPYRA for the treatment of MS; SPINRAZA for the treatment of SMA; SKYCLARYS for the treatment of Friedreich's Ataxia; QALSODY for the treatment of ALS, and FUMADERM for the treatment of severe plaque psoriasis. It also collaborations with Eisai on the commercialization of LEQEMBI for the treatment of Alzheimer's disease and Sage on the commercialization of ZURZUVAE for the treatment of Postpartum Depression (PPD).
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Events Timeline

(ET)
2026-05-08
05:20:00
Eisai and Biogen FDA Review Period Extended to August 24
select
2026-05-07 (ET)
2026-05-07
17:30:00
Remitly Global to Replace Apellis Pharmaceuticals
select

News

Newsfilter
9.0
05-08Newsfilter
PinnedFDA Extends LEQEMBI Review Period by Three Months
  • Review Period Extension: The FDA has extended the review period for LEQEMBI's supplemental Biologics License Application by three months, with a new action date set for August 24, 2026, indicating the agency's significant attention to the drug.
  • Data Support: Eisai and Biogen believe that the comprehensive clinical data package for LEQEMBI strongly supports its potential use as an initiation therapy for early Alzheimer's disease, which is expected to provide patients with more treatment options.
  • Global Recognition: LEQEMBI has been approved by over 50 regulatory authorities worldwide, reflecting broad confidence in its efficacy as a treatment option for early Alzheimer's disease, thereby enhancing its competitive position in the market.
  • Risk Management: The FDA has not raised any concerns regarding the approvability of LEQEMBI during the review process, and Eisai and Biogen are committed to ongoing discussions with the FDA to expedite the delivery of this important advancement to patients.
Yahoo Finance
9.0
05-08Yahoo Finance
Biogen and Eisai FDA Review Extended
  • FDA Review Extension: Biogen and Eisai announced that the U.S. Food and Drug Administration (FDA) has extended the review period for their new drug application, with the specific duration of the extension yet to be disclosed, which may impact the drug's market launch timeline and investor expectations.
  • Potential Market Reaction: The extension of the FDA review could lead to short-term volatility in the stock prices of Biogen and Eisai, particularly given the high market anticipation surrounding the new drug's approval.
  • R&D Progress Uncertainty: This review extension may indicate that the FDA has further concerns regarding the drug's safety or efficacy, potentially requiring additional data, which could affect the companies' R&D timelines and resource allocation.
  • Need for Strategic Adjustment: In light of the FDA review extension, Biogen and Eisai may need to reassess their market strategies and R&D directions to ensure they maintain a competitive edge in the rapidly evolving biopharmaceutical market.
NASDAQ.COM
9.0
05-08NASDAQ.COM
FDA Extends LEQEMBI Review Period
  • Review Extension: The FDA has extended the review period for LEQEMBI as a starting dose for early Alzheimer's disease treatment by three months, with the new PDUFA action date set for August 24, 2026, indicating ongoing regulatory scrutiny.
  • Additional Information Request: During the review process, the FDA requested further information but raised no concerns regarding the drug's approvability, suggesting a positive outlook for LEQEMBI's market potential.
  • International Approval Status: LEQEMBI has been approved in over 50 countries for the treatment of early Alzheimer's disease, reflecting its broad acceptance and potential commercial value in the global market.
  • Market Impact Analysis: This review extension may influence Eisai and Biogen's market strategies, particularly regarding the anticipated launch timeline, necessitating adjustments in their marketing plans to align with the new schedule.
seekingalpha
9.0
05-08seekingalpha
FDA Extends Review Period for Leqembi IQLIK Injection
  • Review Period Extension: The FDA has announced a three-month extension for the review of the supplemental application for Leqembi IQLIK subcutaneous injection, with the new PDUFA date set for August 24, 2026, indicating the agency's commitment to thorough evaluation.
  • Additional Information Request: As part of the review process, the FDA requested additional information, classifying it as a major amendment to the sBLA, which allows sufficient time for a comprehensive review of the new materials, ensuring data integrity.
  • Optimistic Approval Outlook: To date, the FDA has not raised any concerns regarding the approvability of Leqembi IQLIK as an initial treatment option for early Alzheimer's disease, suggesting a favorable market outlook for the drug.
  • Market Impact Analysis: The collaboration between Biogen and Eisai is particularly significant in this context, as it is expected to positively influence future revenues and market share, especially in the competitive landscape of Alzheimer's disease treatments.
PRnewswire
9.0
05-08PRnewswire
FDA Extends LEQEMBI Review Period by Three Months
  • Review Period Extension: The FDA has extended the review period for LEQEMBI's supplemental Biologics License Application by three months, with a new action date set for August 24, 2026, allowing for a thorough review of additional materials, which may impact the drug's market entry timeline.
  • Clinical Data Support: Eisai and Biogen assert that the comprehensive clinical data package for LEQEMBI strongly supports its potential use as an initiation therapy for early Alzheimer's disease, which, if approved, would provide patients with more treatment options and enhance market competitiveness.
  • Global Regulatory Confidence: LEQEMBI has been approved by over 50 regulatory authorities worldwide, reflecting broad confidence in its efficacy as a treatment option for early Alzheimer's disease, which will help bolster the companies' reputations and sales potential in the global market.
  • Safety Concerns: In clinical trials, the incidence of ARIA with LEQEMBI was reported at 21% compared to 9% for placebo, indicating the need for enhanced monitoring and risk management strategies during its rollout to ensure patient safety and minimize adverse reactions.
CNBC
9.5
04-30CNBC
Eli Lilly Reports Strong Q1 Performance with Revenue Surge
  • Significant Revenue Growth: Eli Lilly reported Q1 revenue of $19.8 billion, a 56% year-over-year increase that surpassed the market expectation of $17.6 billion, demonstrating strong performance in the obesity drug market and reinforcing investor confidence in the stock.
  • Earnings Surge: Adjusted earnings per share reached $8.55, more than doubling from last year and exceeding the consensus estimate of $6.66, indicating the company's ability to achieve profitability despite declining drug prices.
  • Competitive Market Dynamics: Despite competition from Novo Nordisk, CEO David Ricks emphasized that the company can overcome price declines through higher volumes, with U.S. drug prices down 7% but volumes up 49%, showcasing strong demand for its GLP-1 products.
  • New Drug Launch and Market Outlook: The recently launched obesity drug Foundayo received FDA approval and became available quickly; although initial growth has been slow, 80% of prescriptions are from patients who had not previously used GLP-1 drugs, suggesting potential to expand the market size.
Wall Street analysts forecast BIIB stock price to rise
26 Analyst Rating
Wall Street analysts forecast BIIB stock price to rise
11 Buy
14 Hold
1 Sell
Moderate Buy
Current: 0.000
sliders
Low
143.00
Averages
204.45
High
246.00
Current: 0.000
sliders
Low
143.00
Averages
204.45
High
246.00
Freedom Broker
Ilya Zubkov
Hold
to
Buy
upgrade
$185 -> $245
AI Analysis
2026-05-01
Reason
Freedom Broker
Ilya Zubkov
Price Target
$185 -> $245
AI Analysis
2026-05-01
upgrade
Hold
to
Buy
Reason
Freedom Broker analyst Ilya Zubkov upgraded Biogen (BIIB) to Buy from Hold with a price target of $245, up from $185. The firm views the company's acquisition of Apellis (APLS) as "strategically sound" and a "necessary step given the expected revenue headwinds from an aging product portfolio." The deal should support Biogen's near-term results and partially reverse its anticipated revenue decline trajectory, the analyst tells investors in a research note. Freedom sees the acquisition as reshaping Biogen's growth narrative.
Truist
Hold
maintain
$189 -> $190
2026-05-01
Reason
Truist
Price Target
$189 -> $190
2026-05-01
maintain
Hold
Reason
Truist raised the firm's price target on Biogen to $190 from $189 and keeps a Hold rating on the shares. The firm has updated its model after the company's Q1 results, also maintaining its concerns regarding Biogen's forward revenue growth trajectory, the analyst tells investors in a research note.
Unlock Full Analyst Thesis, Get the complete breakdown of rating reason for BIIB
Unlock Now

Valuation Metrics

The current forward P/E ratio for Biogen Inc (BIIB.O) is 13.55, compared to its 5-year average forward P/E of 13.90. For a more detailed relative valuation and DCF analysis to assess Biogen Inc'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
13.90
Current PE
13.55
Overvalued PE
17.41
Undervalued PE
10.39

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
10.38
Current EV/EBITDA
9.94
Overvalued EV/EBITDA
12.76
Undervalued EV/EBITDA
8.01

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
3.34
Current PS
2.74
Overvalued PS
4.16
Undervalued PS
2.53

Financials

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Whales Holding BIIB

M
Mubadala Investment Company PJSC
Holding
BIIB
+66.70%
3M Return
C
Capula Management Ltd
Holding
BIIB
+20.27%
3M Return
P
PRIMECAP Management Company
Holding
BIIB
+17.53%
3M Return
M
MAPFRE Asset Management
Holding
BIIB
+17.50%
3M Return
P
Portolan Capital Management, LLC
Holding
BIIB
+16.97%
3M Return
B
Brevan Howard Capital Management LP
Holding
BIIB
+16.14%
3M Return

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Frequently Asked Questions

What is Biogen Inc (BIIB) stock price today?

The current price of BIIB is 193.45 USD — it has increased 1.08

What is Biogen Inc (BIIB)'s business?

Biogen Inc. is a global biopharmaceutical company. The Company is focused on discovering, developing, and delivering advanced therapies for people living with serious and complex diseases worldwide. It operates a portfolio of medicines to treat multiple sclerosis (MS), spinal muscular atrophy (SMA), Alzheimer's disease, and amyotrophic lateral sclerosis (ALS). It is focused on advancing its pipeline in neurology, specialized immunology, and rare diseases. Its marketed products include TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, TYSABRI and FAMPYRA for the treatment of MS; SPINRAZA for the treatment of SMA; SKYCLARYS for the treatment of Friedreich's Ataxia; QALSODY for the treatment of ALS, and FUMADERM for the treatment of severe plaque psoriasis. It also collaborations with Eisai on the commercialization of LEQEMBI for the treatment of Alzheimer's disease and Sage on the commercialization of ZURZUVAE for the treatment of Postpartum Depression (PPD).

What is the price predicton of BIIB Stock?

Wall Street analysts forecast BIIB stock price to rise over the next 12 months. According to Wall Street analysts, the average 1-year price target for BIIB is204.45 USD with a low forecast of 143.00 USD and a high forecast of 246.00 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 Biogen Inc (BIIB)'s revenue for the last quarter?

Biogen Inc revenue for the last quarter amounts to 2.48B USD, increased 1.93

What is Biogen Inc (BIIB)'s earnings per share (EPS) for the last quarter?

Biogen Inc. EPS for the last quarter amounts to 2.15 USD, increased 31.10

How many employees does Biogen Inc (BIIB). have?

Biogen Inc (BIIB) has 7500 emplpoyees as of May 10 2026.

What is Biogen Inc (BIIB) market cap?

Today BIIB has the market capitalization of 28.56B USD.