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Biogen

Biogen logo
🇺🇸United States
Ownership
Private
Established
1978-01-01
Employees
7.5K
Market Cap
$29.6B
Website
https://www.biogen.com
Introduction

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.

Clinical Trials

522

Active:17
Completed:363

Trial Phases

6 Phases

Early Phase 1:2
Phase 1:176
Phase 2:99
+3 more phases

Drug Approvals

9

FDA:9

Drug Approvals

Vumerity

Approval Date
Mar 25, 2024
FDA

Tecfidera

Approval Date
Mar 14, 2024
FDA

TYSABRI

Approval Date
Oct 27, 2023
FDA

Byooviz

Approval Date
Oct 6, 2023
FDA

Aduhelm

Approval Date
Aug 31, 2023
FDA

AVONEX

Approval Date
Jul 31, 2023
FDA

Plegridy

Approval Date
Jul 31, 2023
FDA

QALSODY

Approval Date
Apr 25, 2023
FDA

Spinraza

Approval Date
Feb 24, 2023
FDA

Clinical Trials

Distribution across different clinical trial phases (418 trials with phase data)• Click on a phase to view related trials

Phase 1
176 (42.1%)
Phase 2
99 (23.7%)
Phase 3
94 (22.5%)
Phase 4
42 (10.0%)
Not Applicable
5 (1.2%)
Early Phase 1
2 (0.5%)

A Study to Learn if Taking BIIB141 (Omaveloxolone) Affects How Omeprazole is Processed in the Body and About BIIB141's Safety in Healthy Adults Aged 18 to 55

Not Applicable
Recruiting
Conditions
Healthy Volunteer
Interventions
First Posted Date
2025-09-02
Last Posted Date
2025-09-19
Lead Sponsor
Biogen
Target Recruit Count
22
Registration Number
NCT07149415
Locations
🇺🇸

Austin Clinical Research Unit, Austin, Texas, United States

A Study to Learn About the Safety of BIIB142 and How it is Processed in the Body of Healthy Adult Participants Aged 18 to 55 Years Old

Not Applicable
Recruiting
Conditions
Healthy Volunteer
Interventions
Drug: BIIB142
Drug: BIIB142-Matching Placebo
First Posted Date
2025-08-21
Last Posted Date
2025-09-11
Lead Sponsor
Biogen
Target Recruit Count
78
Registration Number
NCT07133828
Locations
🇺🇸

PPD Development, LP, Las Vegas, Nevada, United States

A Study to Learn More About How Zuranolone Affects Postpartum Depression Symptoms in Participants Who Took it Within 1 Year After The End of Their Pregnancy

Recruiting
Conditions
Depression, Postpartum
Interventions
First Posted Date
2025-07-02
Last Posted Date
2025-08-03
Lead Sponsor
Biogen
Target Recruit Count
200
Registration Number
NCT07047820
Locations
🇺🇸

CVS Health, Woonsocket, Rhode Island, United States

A Study to Learn How BIIB141 (Omaveloxolone) is Processed in the Body When Taken as Capsules Compared to Sprinkled on Yogurt in Healthy Adults Aged 18 to 55

Phase 1
Completed
Conditions
Healthy Volunteer
Interventions
First Posted Date
2025-06-13
Last Posted Date
2025-09-22
Lead Sponsor
Biogen
Target Recruit Count
52
Registration Number
NCT07019064
Locations
🇺🇸

Trialmed formerly PPD, Austin Clinic, Austin, Texas, United States

A Study to Learn More About the Effects and Safety of Felzartamab Infusions in Adults With Primary Membranous Nephropathy (PMN)

Phase 3
Recruiting
Conditions
Primary Membranous Nephropathy
Interventions
Drug: Standard of Care IST
First Posted Date
2025-05-08
Last Posted Date
2025-07-28
Lead Sponsor
Biogen
Target Recruit Count
180
Registration Number
NCT06962800
Locations
🇺🇸

James J Peters Veterans Administration Medical Center - NAVREF - PPDS, Bronx, New York, United States

🇺🇸

Academic Medical Research Institute, Los Angeles, California, United States

🇺🇸

Elixia Health - Michigan Kidney Consultants, LLC - Elixia - PPDS, Pontiac, Michigan, United States

and more 1 locations
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News

Indivi and Clouds of Care Partner to Advance Deep Phenotyping Technologies for Alzheimer's and Parkinson's Drug Development

Two TechBio companies, Indivi and Clouds of Care, announced a strategic partnership to advance precision medicine tools in early-phase neuroscience drug development for Alzheimer's and Parkinson's disease.

CD40-Targeted Therapies Advance Toward First Approval by 2027 with Over 35 Candidates in Clinical Development

Over 35 CD40-targeted therapies are currently in clinical trials, with the first approval expected by 2027 according to new market research.

Stoke Therapeutics Appoints Ian Smith as CEO as Phase 3 Trial for Dravet Syndrome Treatment Advances

Stoke Therapeutics has appointed Ian Smith as Chief Executive Officer after he served as Interim CEO since March 2025, bringing over 30 years of rare disease drug development experience.

Ultragenyx Appoints Eric Olson as Chief Business Officer to Lead Rare Disease Pipeline Expansion

Ultragenyx Pharmaceutical appointed Eric Olson as Chief Business Officer and Executive Vice President effective September 22, 2025, following Thomas Kassberg's planned retirement after 14 years with the company.

Biogen Acquires Alcyone Therapeutics for $85M to Advance Implantable Drug Delivery System for Neurological Therapies

Biogen will acquire Alcyone Therapeutics for $85 million upfront plus development milestones to gain full rights to the ThecaFlex DRx implantable drug delivery system.

Drug Hunter Secures Seed Investment to Expand Knowledge Platform for Pharmaceutical R&D

Drug Hunter, a knowledge platform serving over 200 pharmaceutical R&D organizations including Eli Lilly, Biogen, and NIH, announced seed funding led by Teamworthy Ventures to accelerate drug discovery insights.

FDA Moves to Eliminate Expert Advisory Panels for Individual Drug Reviews Under Trump Administration

The FDA under President Trump is abandoning its decades-old policy of convening outside expert panels to review individual drug applications, with officials claiming these meetings are redundant and time-consuming.

GE HealthCare Acquires Icometrix to Strengthen Brain MRI Analysis Capabilities for Alzheimer's Drug Monitoring

GE HealthCare has acquired brain analysis company Icometrix for an undisclosed sum to expand its Alzheimer's disease diagnostic capabilities.

FDA Accepts IND Application for BIIB142, First IRAK4 Degrader to Enter Clinical Development for Autoimmune Diseases

The FDA has accepted Biogen's IND application for BIIB142, an IRAK4 protein degrader developed through collaboration with C4 Therapeutics, marking the first IRAK4 degrader to advance toward clinical trials for autoimmune diseases.

FDA Approves Weekly Autoinjector for Eisai's Alzheimer's Drug Leqembi, Enabling At-Home Treatment

The FDA has approved a once-weekly autoinjector version of Eisai's Alzheimer's drug Leqembi, branded as Leqembi IQLIK, marking the first at-home dosing option for amyloid-based Alzheimer's therapy.

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