Latest News - Biogen

Top Corporates Hub

Biogen

BIIB | NASDAQ | United States
865
-305
Rank
$32.85B
Market Cap
$9.67B
-$ 0.16B
-1.63%
Revenue
$1.90B
+$ 0.61B
+47.29%
Earnings
7.6K
+0K
+0.46%
Employees
Ionis Pharmaceuticals Eyes Big Year With TRYNGOLZA Decision, 5 Phase 3 Readouts

26.05.2026 00:06

Ionis Pharmaceuticals (NASDAQ:IONS) highlighted a busy slate of regulatory decisions, clinical readouts and partnered programs during a presentation at RBC Capital Markets’ Global Healthcare Conference, with Chief Development Officer Holly Kordasiewicz saying the company is moving from recent launch

Read More

Immunic Appoints Seasoned Biopharmaceutical Executive Michael W. Bonney as Chair of the Board of Directors

19.05.2026 10:30

Immunic, Inc. (Nasdaq: IMUX), a late-stage biotechnology company pioneering the development of novel oral therapies for neurologic diseases, today announced the appointment of Michael "Mike" W. Bonney, a highly experienced biopharmaceutical executive and board leader, as Chair of its Board of Directors, effective May 16, 2026. Simona Skerjanec, M.Pharm, MBA, will transition from Interim Chairperson to continue serving as a member of the Board.

Read More

How The Alector (ALEC) Investment Story Is Shifting With Tau Readthroughs And BBB Shuttle Focus

19.05.2026 04:34

Alector’s updated analyst framework now points to a fair value move from US$2.88 to US$3.10, a modest shift that still signals a meaningful recalibration of expectations. This change is closely tied to how analysts are weighing CELIA’s readthrough for tau-targeting therapies and Alector’s pivot toward blood brain barrier shuttle based designs, balancing the scientific promise against execution risks and the memory of prior trial setbacks. As you read on, you will see how to track these moving...

Read More

BIIB SHAREHOLDER INVESTIGATION: SueWallSt Investigates Biogen Inc. for Possible Securities Law Violations

18.05.2026 09:03

Biogen Phase 2 CELIA trial data sent shares down 6.4% after it was revealed that topline data missed its primary endpoint.NEW YORK, May 18, 2026 /PRNewswire/ -- Biogen Inc. shareholders lost 6.4% per...

Read More

Cisco upgraded, Doximity downgraded: Wall Street's top analyst calls

15.05.2026 13:45

Cisco upgraded, Doximity downgraded: Wall Street's top analyst calls

Read More

Biogen completes $5.3B Apellis Pharmaceuticals acquisition

15.05.2026 11:44

Apellis, maker of eye disease drug SYFOVRE and kidney drug EMPAVELI, is now a wholly owned Biogen subsidiary

Read More

Biogen: Apellis Acquisition, Alzheimer's Fail Sums Up Mixed Investment Opportunity

15.05.2026 11:10

Biogen Inc. upgraded to Hold: Apellis deal adds revenue, MS stable but pipeline delays persist. Click for this updated look at BIIB following Q1 earnings.

Read More

The ADDF Highlights Encouraging Progress Toward Targeting Multiple Alzheimer's Pathologies in Biogen's Phase 2 Tau Study

15.05.2026 00:48

Today, Biogen announced topline results from the Phase 2 CELIA study of diranersen, an investigational therapy designed to target tau in people with early Alzheimer's disease. While the study did not meet its primary endpoint, Biogen reported reductions in tau and signals of slowed cognitive decline and plans to advance the drug into further trials.

Read More

Ionis partner Biogen announces topline results from Phase 2 CELIA study of diranersen (BIIB080): first study to show reduction in tau pathology and cognitive benefit in patients with early Alzheimer’s disease

14.05.2026 11:05

CARLSBAD, Calif., May 14, 2026--Ionis Pharmaceuticals, Inc. (Nasdaq: IONS) today announced that its partner, Biogen, shared compelling topline results from the Phase 2 CELIA study evaluating diranersen (IONIS-MAPTRx/BIIB080), an investigational antisense oligonucleotide (ASO) therapy targeting tau, in individuals with early Alzheimer’s disease (AD). The CELIA results provide the first evidence from a randomized Phase 2 study of a tau-directed therapy demonstrating both robust biomarker impact an

Read More

Topline Results from Phase 2 CELIA Study of Diranersen (BIIB080): First Study to Show Reduction in Tau Pathology and Cognitive Benefit in Patients with Early Alzheimer’s Disease

14.05.2026 10:59

CELIA did not meet its primary endpoint assessing dose response; based on the strength of the biomarker and efficacy data, Biogen plans to advance diranersen to registrational developmentRobust reductions in tau pathology were observed across all studied doses, with results generally consistent with those observed in the Phase 1b study1Pre-specified analyses of cognitive endpoints demonstrated slowing of clinical decline across all studied doses, particularly at the lowest doseThe safety and tol

Read More

Biogen to advance experimental Alzheimer's drug despite mid-stage trial miss

14.05.2026 08:08

Biogen said on Thursday itwas advancing its experimental Alzheimer’s drug to late-stagetrials despite the treatment failing to meet the main goal of amid-stage study. Shares of the...

Read More

Topline results from phase 2 Celia study of diranersen, first study to show reduction in tau pathology and cognitive benefit in patients with early Alzheimer's disease

14.05.2026 07:45

Biogen Inc: Topline results from phase 2 Celia study of diranersen : first study to show reduction in tau pathology and cognitive benefit in patients with early Alzheimer's disease Biogen -...

Read More

3 Healthcare Stocks We’re Skeptical Of

14.05.2026 04:52

Healthcare companies are pushing the status quo by innovating in areas like drug development and digital health. Despite the rosy long-term prospects, short-term headwinds such as COVID inventory destocking have caused the industry to lag recently - over the past six months, the collective 3.7% gain for healthcare stocks has fallen short of the S&P 500’s 7.1% rise.

Read More

Biogen Inc. (BIIB) Presents at Bank of America Global Healthcare Conference 2026 Transcript

13.05.2026 17:10

Biogen Inc. (BIIB) Bank of America Global Healthcare Conference 2026 May 13, 2026 2:20 PM EDTCompany ParticipantsAdam MeyersConference Call...

Read More

Transcript : Biogen Inc. Presents at Bank of America Global Healthcare Conference 2026, May-13-2026 11

13.05.2026 15:35

Presenter SpeechJason Zemansky Annual Healthcare Conference in Tasty Las Vegas. My name is Jason Zemansky. I'm one of the mid-cap analysts here at the bank. Very pleased to have join me Biogen and...

Read More

3 Value Stocks We Approach with Caution

12.05.2026 10:28

Value investing has produced some of the world’s most famous investing billionaires, including Warren Buffett, David Einhorn, and Seth Klarman, who built their fortunes by purchasing wonderful businesses at reasonable prices. But these hidden gems are few and far between - many stocks that appear cheap often stay that way because they face structural issues.

Read More

Is Biogen Inc. (BIIB) one of the Best Biotech Stocks to Invest In According to Billionaire Steve Cohen?

12.05.2026 00:05

Biogen Inc. (NASDAQ:BIIB) is the Best Biotech Stock. On April 20, 2026, Reuters reported that Biogen Inc. (NASDAQ:BIIB) had agreed to pay up to $850 million for the exclusive Greater China rights to felzartamab. It is an experimental immune therapy developed by Chinese biotech TJ Biopharma, bringing the drug’s global commercial coverage to a close. TJ […]

Read More

Update on FDA Priority Review of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection as a Starting Dose for Early Alzheimer’s Disease

08.05.2026 06:30

TOKYO and CAMBRIDGE, Mass., May 08, 2026 (GLOBE NEWSWIRE) -- Eisai Co., Ltd. and Biogen Inc. (Nasdaq: BIIB) today announced that the U.S. Food and Drug Administration (FDA) has extended the review period by three months for the supplemental Biologics License Application (sBLA) for a once-weekly lecanemab-irmb subcutaneous injection (U.S. brand name: LEQEMBI® IQLIK™) as a starting dose for the treatment of early Alzheimer’s disease. The new Prescription Drug User Fee Act (PDUFA) action date is Au

Read More

Update on FDA Priority Review of LEQEMBI® IQLIK™ (lecanemab-irmb) Subcutaneous Injection as a Starting Dose for Early Alzheimer's Disease

08.05.2026 06:30

Eisai Co., Ltd. and Biogen Inc. (Nasdaq: BIIB) today announced that the U.S. Food and Drug Administration (FDA) has extended the review period by three months for the supplemental Biologics License Application (sBLA) for a once‑weekly lecanemab‑irmb subcutaneous injection (U.S. brand name: LEQEMBI® IQLIK™) as a starting dose for the treatment of early Alzheimer's disease. The new Prescription Drug User Fee Act (PDUFA) action date is August 24, 2026.

Read More