Revenue segments as reported by the company.

Product, net

Revenue from anti-CD20 therapeutic programs

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Revenue from LEQEMBI Collaboration

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Gross Profit, Operating Income, and Net Income as a percentage of Revenue

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An operating expense is an expense a business incurs through its normal business operations. Often abbreviated as OPEX.

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(Gain) loss on divestiture of Hillerød, Denmark manufacturing operations

(Gain) loss on fair value remeasurement of contingent consideration

Acquired in-process research and development

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Gain on sale of building

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Year over year growth in Revenue and Operating Expenses.

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Shares outstanding refer to a company's stock currently held by all its shareholders, including share blocks held by institutional investors and restricted shares owned by the company's officers and insiders.

Outstanding Shares

Market Cap

Also known as Price/Sales Ratio. Calculated using Average market cap for the quarter / Annualized quarterly revenue.

Revenue Multiple

Biogen

Biogen, Inc. is a biopharmaceutical company, which engages in discovering, developing, and delivering therapies for neurological and neurodegenerative diseases. It offers TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, TYSABRI, and FAMPYRA for the treatment of multiple sclerosis, SPINRAZA for the treatment of spinal muscular atrophy, and FUMADERM for the treatment of severe plaque psoriasis. The company was founded by Charles Weissmann, Heinz Schaller, Kenneth Murray, Walter Gilbert, and Phillip Allen Sharp in 1978 and is headquartered in Cambridge, MA.

Earnings data Q1 2021

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Biogen reports Q4 results, focuses on cost-saving and growth strategies

Biogen's Q4 2022 performance showed a revenue decline but an increase in non-GAAP diluted EPS.
The company is prioritizing cost-saving initiatives and strategic product launches for growth.
Challenges include managing expenses, evaluating R&D programs, and balancing cost reductions with investments.
Opportunities lie in upcoming product launches, potential acquisitions, and expanding into new therapeutic areas.

Biogen reports $2.5B revenue in Q1 2023, focuses on transformative drug launches

Biogen's Q1 2023 performance showed revenue stability despite challenges in MS product revenue.
The company's strengths lie in its focus on transformative drug launches and Alzheimer's research advancements.
Challenges include reimbursement expectations and managing the transition period until 2025.
Opportunities exist in external growth strategies, asset prioritization, and commercial launches for LEQEMBI and Zuranolone.

Biogen reports mixed Q2 earnings, LEQEMBI approval drives optimism

Biogen's Q2 2023 Earnings Call showcased mixed financial performance, with a focus on cost-saving initiatives and pipeline advancements. LEQEMBI's approval and positioning as a maintenance treatment offer promise, while challenges in revenue decline and market adoption persist. Strategic initiatives and upcoming milestones provide opportunities for growth and portfolio enhancement.

Biogen reports solid Q3 earnings, eyes regulatory approvals and market expansion

Biogen's Q3 2023 performance reflects steady growth, strategic initiatives, and promising product developments.
Strengths in sustainable growth priorities, product launches, and cost optimization position Biogen for long-term success.
Challenges in market expansion and operational efficiency require focused efforts on infrastructure and process improvements.
Opportunities in regulatory approvals, market expansion, and therapeutic advancements pave the way for future growth and innovation.

Biogen reports Q4 revenue decline but eyes growth opportunities

Biogen's Q4 2023 performance saw revenue decline offset by growth in rare disease revenue.
The company's strategic strengths lie in new product launches, cost reduction initiatives, and a focused pipeline strategy.
Challenges include bottlenecks in product launches and trial size reductions, while opportunities exist in upcoming milestones and market expansion.
Overall, Biogen aims for sustainable growth with a diversified product portfolio and strategic market focus.

Biogen reports robust Q1 earnings, focuses on market expansion

Biogen's Q1 performance reflects strong earnings growth and strategic focus on new launches. Despite challenges in launch processes, the company is capitalizing on market penetration opportunities. With a robust balance sheet and ongoing market expansion efforts, Biogen is poised for continued growth and success.

Biogen reports robust Q2 earnings, eyes growth in new launches

Biogen's Q2 2024 earnings call highlighted strong financial performance, successful product launches, and strategic priorities for growth. While challenges in the MS franchise persist, the company remains focused on sustainable growth through R&D investments and acquisitions. Opportunities for growth exist in expanding product portfolios and upcoming data releases.

Biogen reports mixed Q3 results, focuses on growth strategies

Biogen's Q3 2024 performance was mixed, with revenue growth in key products but overall revenue decline.
The company faces challenges in certain product segments but shows strength in new product development.
Opportunities lie in expanding market presence, new product launches, and potential business development.
Despite profitability challenges, Biogen's focus on growth strategies positions it for future success.

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Biogen, Inc. is a biopharmaceutical company, which engages in discovering, developing, and delivering therapies for neurological and neurodegenerative diseases. Its products include TECFIDERA, VUMERITY, AVONEX, PLEGRIDY, TYSABRI and FAMPYRA for the treatment of MS, SPINRAZA for the treatment of SMA, ADUHELM for the treatment of Alzheimer's disease, and FUMADERM for the treatment of severe plaque psoriasis. The company was founded by Charles Weissmann, Heinz Schaller, Kenneth Murray, Walter Gilbert, and Phillip Allen Sharp in 1978 and is headquartered in Cambridge, MA.

Wall Street analysts suggest that Biogen Inc (NASDAQ: BIIB) stock is about to see a significant selloff and could witness volatility until the Food and Drugs Administration (FDA) review process comes to a close in March 2021, Bloomberg reports. The analyst forecasts were based on expectations that the company's developmental treatment for Alzheimer's disease, Aducanumab, would not be approved by the FDA.

Analysts Predict Volatility In Biogen Shares Until March 2021

CAMBRIDGE, Mass. and TOKYO, Nov. 06, 2020 (GLOBE NEWSWIRE) -- Today, the U.S. Food and Drug Administration (FDA) Peripheral and Central Nervous System Drugs Advisory Committee voted 1 yes, 8 no and 2 uncertain on the question, “Does Study 302 (EMERGE), viewed independently and without regard for Study 301 (ENGAGE), provide strong evidence that supports the effectiveness of aducanumab for the treatment of Alzheimer's disease?”. The Advisory Committee also voted 0 yes, 7 no and 4 uncertain on the question, “Does Study 103 (PRIME) provide supportive evidence of the effectiveness of aducanumab for the treatment of Alzheimer's disease?”, and 5 yes, 0 no and 6 uncertain on the question, “Has the Applicant presented strong evidence of a pharmacodynamic effect of aducanumab on Alzheimer's disease pathophysiology?”. Finally, the Advisory Committee voted 0 yes, 10 no and 1 uncertain on the question, “In light of the understanding provided by the exploratory analyses of Study 301 and Study 302, along with the results of Study 103 and evidence of a pharmacodynamic effect on Alzheimer's disease pathophysiology, it is reasonable to consider Study 302 as primary evidence of effectiveness of aducanumab for the treatment of Alzheimer's disease?”

Update on FDA Advisory Committee's Meeting on Aducanumab in Alzheimer's Disease

NEW YORK, Nov. 6, 2020 /PRNewswire/ -- An independent FDA advisory committee today signaled in several votes that it does not believe the clinical study data for Biogen's aducanumab supports the drug's approval for patients with early stage Alzheimer's disease. "Although today's...

Alzheimer's Drug Discovery Foundation Statement on Today's FDA Independent Panel Vote on Biogen's Aducanumab

The committee of outside experts saw right through the FDA's cheerleading.

FDA Committee Votes Strongly Against Biogen's Alzheimer's Disease Drug

The future of an experimental Alzheimer's drug was thrown back into substantial doubt on Friday, as an influential expert panel concluded the treatment had not shown enough evidence of effectiveness.  The committee's negative recommendations came in stark contrast to the FDA's own position. In briefing documents released Wednesday, the regulatory agency stated there was "substantial evidence of effectiveness to support approval."

An influential group of health experts rejects Biogen's experimental Alzheimer's drug, casting substantial doubt over the drug's chances of approval (BIIB)

Biogen Inc (NASDAQ: BIIB) failed to win the backing of the FDA panel which reviewed the BLA for its controversial Alzheimer's drug aducanumab, an antibody which targets amyloid-beta. What Happened: FDA's Peripheral and Central Nervous System Drugs Advisory Committee met Friday to discuss the BLA voted with eight 'no' votes and 'one' yes vote on the question of whether the Phase 3 Study 302, viewed independently and without regard for the failed Study 301, provided strong evidence supporting the effectiveness of aducanumab for the treatment of Alzheimer's disease.

Biogen's Aducanumab Fails To Win FDA Panel Backing

If fully approved, it would be the first drug to slow cognitive decline in people living with the disease and the first new treatment for Alzheimer's in nearly 20 years.

Biogen hits snag after Alzheimer's drug fails to win support from FDA panel

Biogen Inc. BIIB appears to have suffered a setback on Friday at the hands of a Food and Drug Administration advisory panel over recommendation to approve its experimental Alzheimer's disease treatment. On Friday, the FDA's Peripheral and Central Nervous System Drugs Advisory Committee voted 8 to 1 against recommending approval of Biogen's treatment aducanumab, while two members cast “undecided” votes, according to reports and multiple tweets Friday.

Biogen Alzheimer's drug appears to have setback as FDA advisers recommend not to approve

The stock price of Biogen Inc (NASDAQ: BIIB) has received a price target increase from $342 to $402 by SVB Leerink. These are the details.

BIIB Stock: $402 Price Target By SVB Leerink

Biogen stock was halted early Friday ahead of a Food and Drug Administration advisory committee meeting to discuss the fate of its controversial Alzheimer's treatment, aducanumab. The post Biogen Stock Halted As FDA Panel Prepares To Discuss Alzheimer's Drug appeared first on Investor's Business Daily.

Biogen Stock Halted As FDA Panel Prepares To Discuss Alzheimer's Drug

A panel of outside experts meets Friday to advise the Food and Drug Administration on aducanumab, a drug from Cambridge, Massachusetts-based Biogen Inc. and Japan's Eisai Co. FDA doesn't always follow the panel's advice but usually does and has until March to decide.

FDA panel reviews 1st new Alzheimer's drug in 2 decades

Shares of Biogen were halted in premarket trading on Friday in advance of a meeting that will have medical experts discuss whether or not the Food and Drug Administration should approve the company's experimental Alzheimer's disease drug. The advisory committee is expected to make a recommendation to the FDA at the end of the meeting; the regulator is not required to follow the advice of the committee but often does.

Biogen's stock is halted as FDA committee convenes on experimental Alzheimer's disease treatment

Biogen Inc (NASDAQ: BIIB) shares saw a nice 40% bump Wednesday following the release of FDA briefing document prepared for Friday's Adcom meeting to discuss aducanumab BLA. Morgan Stanley analyst Matthew Harrison maintained an Overweight rating and $357 price target.

Biogen Analysts Brace For Favorable Aducanumab Adcom Verdict

Odds are increasing that Biogen's experimental and somewhat controversial Alzheimer's disease drug may get approved after Food and Drug Administration officials said there was enough evidence in clinical trials to prove the therapy's effectiveness.

Signs point to FDA approval for Biogen's experimental Alzheimer's disease treatment, though there are skeptics

Hello, While we wait to hear more about the results of the presidential election, here's the latest in healthcare news.

The promise of the first new Alzheimer's drug in nearly 2 decades

Biogen had a dramatic day, after years of flip-flop, as it appears the company's new Aducanumab drug will be approved. Even outside of Aducanumab, the company has continued to perform well, with an efficient balance sheet and impressive portfolio.

Biogen Changes The World And Grows 44%

Everything Investors Need to Know About Biogen's FDA Meeting Tomorrow

General Motors

Peloton

Wendy's

Biogen, Peloton, General Motors and Wendy's were our top stock trades for Thursday. Now, let's look at the charts to see what's going on.

4 Top Stock Trades for Thursday: BIIB, PTON, GM, WEN

Biogen Inc (NASDAQ: BIIB) shares jumped more than 40% on Wednesday after the company received a favorable FDA briefing related to the company's investigational Alzheimer's drug aducanumab. Despite the huge bullish move, at least one trader is speculating Biogen's big run may be just getting started ahead of Friday's aducanumab Adcom meeting.

Option Trader Bets $2.5M On Biogen After FDA's Favorable Alzheimer's Drug Support

Biogen submitted its application for approval of Alzheimer's treatment aducanumab in early July. And it's still targeting a coronavirus treatment with Vir.

Is Biogen Stock A Buy As FDA Panel Considers Key Alzheimer's Drug?

A close look into why Biogen stock is surging toward its best day ever.

Pharma Stock Eyes Best Day Ever On FDA Backing

Biogen soared as much as 47% on Wednesday after a FDA review panel found the efficacy of its Alzheimer's drug, aducanumab, was "exceptionally persuasive." The FDA's staff said data from a large trial of the experimental drug supports its eventual approval, boosting chances that Biogen's drug could the market for Alzheimer's patients in the future. The next step for the drug to be approved is Friday's review of aducanumab by FDA's independent experts, who will then make a recommendation to the agency.

Biogen soars 47% after FDA scientists say its Alzheimer's drug's efficacy is 'exceptionally persuasive' (BIIB)

The first disease-modifying Alzheimer's drug got a step closer to federal approval on Wednesday, as US regulators signaled support for the controversial treatment's efficacy.  The US Food and Drug Administration released documents summarizing Biogen's application for its experimental drug, aducanumab. Investors were eagerly anticipating these briefing docs to see if they suggest, one way or the other, that the agency is supportive of the drug. 

Biogen just gained $16 billion in market value, as investors increasingly expect approval of the first Alzheimer's drug in over 15 years. Here's what comes next.

Biogen Inc (NASDAQ: BIIB) shares were soaring Wednesday in reaction to an FDA  briefing document released ahead of Friday's Adcom meeting on the investigational Alzheimer's drug aducanumab, an amyloid beta-targeting antibody. What Happened: The Study 302 that evaluated aducanumab showed primary evidence of effectiveness, and the results of Study 103 were appropriately viewed as supportive evidence of the effectiveness, according to the briefing document prepared by Biogen and the FDA for the panel members of the Peripheral and Central Nervous System Drugs Advisory Committee.

Biogen Surges On Favorable FDA Briefing Doc For Alzheimer's Candidate

Shares of Biogen soared 42.2% in trading on Wednesday after the Food and Drug Administration said there is "substantial evidence" that the company's experimental Alzheimer's disease drug is an effective treatment option. The agency's review of the drug, aducanumab, was shared in a document released Wednesday in advance of a planned meeting of an FDA advisory committee on Friday.

News for Biogen Stock (BIIB)