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BIIBNasdaq

BIOGEN INC.

Biological products·Commercial·Cambridge, MA, United States·CEO: Mr. Christopher A. Viehbacher
OncologyRare DiseaseGene TherapyNeurologyImmunologyOphthalmologyInfectious DiseasePainDermatologyNephrology

BIIB evidence brief

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BioSniper AI · BIIB

Biogen Inc. (BIIB) is a biotechnology company focused on neurology, immunology, and rare diseases, with a late-stage pipeline and growth products including SKYCLARYS, QALSODY, ZURZUVAE, and LEQEMBI. As of 2026-03-31, the company reported cash & equivalents of $3,382.7M, total revenue of $2,477.8M, net income of $319.5M, and total debt of $12,577.0M [sec].

Key risk: Pipeline execution risk

8.7/10

BioSniper Score

Based on 6 of 6 signals

Market Cap

$32.28B

Cash Runway

Lead Asset

BIIB080 (Phase 3)

Financial data as of Mar 31, 2026.

Tracking 14 pipeline candidates · 48 clinical trials · 17 catalysts · 7 FDA decisions for BIOGEN INC..

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AI OverviewAI overview is shown in English only.

Biogen Inc. (BIIB) is a biotechnology company focused on neurology, immunology, and rare diseases, with a late-stage pipeline and growth products including SKYCLARYS, QALSODY, ZURZUVAE, and LEQEMBI. As of 2026-03-31, the company reported cash & equivalents of $3,382.7M, total revenue of $2,477.8M, net income of $319.5M, and total debt of $12,577.0M [sec].

  • Biogen increased growth product revenue by 19% year-over-year to $3.3 billion in 2025, led by SKYCLARYS, QALSODY, ZURZUVAE, and VUMERITY [sec · filed 2026-04-28].
  • The company has a high-conviction late-stage pipeline in neurology, immunology, and rare disease, with key milestones including regulatory approvals for LEQEMBI, SKYCLARYS, and QALSODY across major global markets [sec · filed 2026-04-28].
  • As of 2026-03-31, Biogen had cash & equivalents of $3,382.7M, total revenue of $2,477.8M, net income of $319.5M, and total debt of $12,577.0M [sec].
  • Biogen entered strategic collaborations including a partnership with City to develop RNAi therapies, licensing an oral C5aR1 antagonist from Vanqua, and acquiring Alcyone to advance ASO delivery [sec · filed 2026-04-28].
  • The company achieved targeted productivity improvements and exceeded top talent retention goals, while establishing operational manufacturing expansion plans [sec · filed 2026-04-28].

What works

  • Biogen's growth product revenue increased 19% year-over-year to $3.3 billion in 2025, indicating strong commercial execution for newer products like SKYCLARYS, QALSODY, and ZURZUVAE [sec · filed 2026-04-28].
  • The company has a high-conviction late-stage pipeline with multiple Phase 3 trials ongoing, including felzartamab for IgA nephropathy and higher-dose nusinersen for spinal muscular atrophy, providing potential for future growth [sec · filed 2026-04-28].
  • Biogen has established strategic collaborations and acquisitions (e.g., RNAi partnership with City, Vanqua license, Alcyone acquisition) to expand its pipeline and technology platforms [sec · filed 2026-04-28].

What to weigh

  • Non-GAAP diluted earnings per share declined in 2025 compared to 2024, reflecting expected total revenue decline and planned investments in pipeline and launches [sec · filed 2026-04-28].
  • The company faces significant debt of $12,577.0M as of 2026-03-31, which may constrain financial flexibility [sec].
  • Biogen's legacy product performance is under pressure from generic competition, and the company is reliant on growth products to replace mature franchises [sec · filed 2026-04-28].

From the filings

Quoted directly from source documents.

  • Growth product revenue increased 19% year-over-year in 2025

    The Company increased growth product revenue by 19% year-over-year to $3.3 billion, led by SKYCLARYS, QALSODY, ZURZUVAE, VUMERITY

    SEC filings · April 28, 2026

  • Biogen is focused on neurology, immunology, and rare disease pipeline

    a high-conviction late-stage pipeline with the potential to drive both meaningful innovation and sustained growth. We made notable progress on this strategy in 2025, where execution on commercialization of our growth products and a sharpened development pipeline focused on neurology, immunology, and rare disease are laying a strong foundation for Biogen's future.

    SEC filings · April 28, 2026

Catalyst timeline

  • 2027-06-01 · Phase3_Topline · felzartamab — Phase 3 Topline: A Double-Blind, Placebo-Controlled, Multicenter, Randomized Phase 3 Trial Evaluating the Efficacy anTopline data for felzartamab in IgA nephropathy; will inform potential regulatory submission.
  • 2027-09-24 · Phase3_Topline — Phase 3 Topline: A Phase 3b Study to Evaluate Higher Dose Nusinersen (BIIB058) in Patients With Spinal Muscular AtropTopline data for higher-dose nusinersen in SMA; could expand SPINRAZA franchise.
  • 2027-12-14 · Phase3_Topline — Phase 3 Topline: A 2-Part Seamless Part A (Phase 2)/Part B (Phase 3) Randomized, Double-Blind, Placebo-Controlled, MuTopline data from a seamless Phase 2/3 study; specific indication not fully disclosed.
  • 2029-06-05 · Phase3_Topline · felzartamab — Phase 3 Topline: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study of Felzartamab in Adults With IgA NephSecond Phase 3 topline for felzartamab in IgA nephropathy; may support broader label.
  • 2029-06-30 · Phase3_Topline — Phase 3 Topline: A Placebo-Controlled, Double-Blind, Parallel-Group, 18-Month Study With an Open-Label Extension PhasTopline data from an 18-month study with open-label extension; likely for a rare disease candidate.
  • 2029-11-22 · Phase3_Topline — Phase 3 Topline: A Phase 3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of OmaveloxTopline data for omaveloxolone; potential Friedreich's ataxia treatment.
  • 2029-12-11 · Phase3_Topline — Phase 3 Topline: A Multicenter, Open-Label, Single-Arm, Phase 3, Long-Term Extension Study to Evaluate Continuous SafLong-term extension study topline; assesses safety and durability of an existing candidate.
  • 2030-03-29 · Phase3_Topline — Phase 3 Topline: A Multicenter, Randomized, Dose-Blind, Phase 3 Long-Term Extension Study to Evaluate ContinuousLong-term extension study topline; evaluates continuous dosing of a candidate.
Risks & what to watch (4)

Key risks

  • Pipeline execution riskDevelopment programs are subject to high risk and investment; status, timing, and scope may change [sec_mda · as of 2026-02-06].
  • Generic competition for legacy productsBiogen drove legacy product performance despite generic competition, indicating pressure on mature franchises [sec · filed 2026-04-28].
  • High debt burdenTotal debt of $12,577.0M as of 2026-03-31 may limit financial flexibility and increase interest costs [sec].
  • Dependence on growth productsGrowth product revenue is weighted 2.5 times more than total revenue, with ambitious assumptions for launches [sec · filed 2026-04-28].

What to watch

  • Phase 3 topline results for felzartamab in IgA nephropathy expected in 2027 and 2029 [catalyst timeline].
  • Phase 3 topline results for higher-dose nusinersen (BIIB058) in spinal muscular atrophy expected in 2027 [catalyst timeline].
  • Phase 3 topline results for omaveloxolone in an 18-month study expected in 2029 [catalyst timeline].
  • Execution of strategic collaborations (RNAi, Vanqua, Alcyone) and their impact on pipeline advancement [sec · filed 2026-04-28].

Sources: SEC filings · SEC MD&A · Generated August 29, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 6 of 6 signals · derived from public data

Cash Runway10.0

Profitable (positive operating cash flow)

Financial Health8.5

OCF $646M · Net income $320M · Debt/OCF 3.6×

Pipeline Maturity10.0

Lead: Approved

Pipeline Breadth10.0

14 candidates

Catalyst Momentum10.0

17 upcoming, next in ~275d

Insider Signal3.6

0 buys · 2 sells (180d)

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

1,000

Total value held

$25.65B

HolderSharesValue
vanguard capital management llc19,074,834$3.50B
blackrock, inc.15,974,601$2.93B
primecap management co/ca/14,757,607$2.71B
fmr llc12,807,541$2.35B
state street corp7,167,922$1.31B
vanguard portfolio management llc6,531,727$1.20B
geode capital management, llc4,342,602$793.4M
wellington management group llp2,961,641$543.0M
morgan stanley2,170,940$398.0M
aqr capital management llc1,923,557$346.2M

Showing top 10 of 1,000 institutional holders of BIOGEN INC.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
3.4%
Days to cover
3.2
Shares short
4,475,470
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

BIIB short interest

Governance

Frequently asked questions

What is the AI investment thesis for BIOGEN INC.?

Biogen Inc. (BIIB) is a biotechnology company focused on neurology, immunology, and rare diseases, with a late-stage pipeline and growth products including SKYCLARYS, QALSODY, ZURZUVAE, and LEQEMBI. As of 2026-03-31, the company reported cash & equivalents of $3,382.7M, total revenue of $2,477.8M, net income of $319.5M, and total debt of $12,577.0M [sec].

What is BIOGEN INC.'s lead drug candidate?

BIOGEN INC.'s most advanced tracked candidate is BIIB080 (Phase 3) for Healthy Volunteer.

What is BIOGEN INC.'s next catalyst?

BIOGEN INC.'s next tracked catalyst is a Phase3_Topline event — "Phase 3 Topline: A Double-Blind, Placebo-Controlled, Multicenter, Randomized Phase 3 Trial Evaluating the Efficacy an" — expected June 1, 2027.

Who is the CEO of BIOGEN INC.?

Mr. Christopher A. Viehbacher is the chief executive officer of BIOGEN INC. (BIIB).

Where is BIOGEN INC. headquartered?

BIOGEN INC. (BIIB) is headquartered in Cambridge, MA, United States.

925 companies232,681 SEC filings21,417 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.