Biogen
Biogen sponsors 334 registered US clinical trials on ClinicalTrials.gov, 21 of them currently recruiting, and 237 completed. 84 of these trials are in Phase 3-4 (later-stage) and 198 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Multiple Sclerosis, with 13 trials.
Trial Pipeline
334 total, page 6 of 7
BIIB033 Single Ascending Dose Study in Healthy Volunteer Subjects
NCT01052506
BIIB014 Cardiovascular Monitoring Study
NCT01035515
Hormone Receptor Positive Metastatic Breast Cancer (HR+ mBC) BIIB021 Plus Aromasin Schedule Finding
NCT01004081
Effect of Food and Antacid on BIIB021 With Advanced Solid Tumors
NCT01017198
A Study of BIIB022 in Combination With Paclitaxel and Carboplatin in Subjects With Non-Small Cell Lung Cancer
NCT00970580
Sorafenib With BIIB022 in Hepatocellular Carcinoma (HCC)
NCT00956436
Study to Investigate the Effect of GSK1014802 on Ambulatory Blood Pressure
NCT00955396
Efficacy and Safety Study of Peginterferon Beta-1a in Participants With Relapsing Multiple Sclerosis
NCT00906399
Trial to Determine the Effects of Bardoxolone Methyl on eGFR in Patients With Type 2 Diabetes and Chronic Kidney Disease
NCT00811889
BG9928 in Subjects With Hepatic Impairment
NCT00858156
BG00012 Monotherapy Safety and Efficacy Extension Study in Multiple Sclerosis (MS)
NCT00835770
Oral Tonapofylline (BG9928) in Patients With Heart Failure and Renal Insufficiency
NCT00745316
Evaluate the Safe and Effective Use of the Avonex® Single-Use Autoinjector in Multiple Sclerosis Subjects
NCT00828204
Study to Explore the Effect of Mefloquine in Participants With Progressive Multifocal Leukoencephalopathy (PML)
NCT00746941
A Pharmacokinetic (PK) Study of Natalizumab (Tysabri) at Steady State
NCT00744679
BIIB023 (Anti-TWEAK) in Subjects With Rheumatoid Arthritis
NCT00771329
Immunogenicity and Safety of Subcutaneously-administered Avonex (Interferon Beta-1a) in Multiple Sclerosis (MS) Patients
NCT00784836
Study of Natalizumab in Relapsed/Refractory Multiple Myeloma
NCT00675428
Mechanism of Action of Galiximab in Subjects With Previously Untreated Follicular Non-Hodgkin's Lymphoma
NCT00651443
Study to Assess the Safety and Tolerability of IV Tonapofylline in Subjects With Acute Decompensated Heart Failure (ADHF) and Renal Insufficiency
NCT00709865
CD INFORM: Investigating Natalizumab Through Further Observational Research and Monitoring
NCT00707512
Administration of BIIB028 to Subjects With Solid Tumors
NCT00725933
A Phase I Study of BIIB015 in Relapsed/Refractory Solid Tumors
NCT00674947
A Phase 2 Study of Interferon Beta-1a (Avonex®) in Ulcerative Colitis
NCT00616434
Phase IIa Trial to Determine the Effects of Bardoxolone Methyl on Renal Function in Patients With Diabetic Nephropathy
NCT00664027
A Multiple Dose Safety Study of PEG-IFN in Healthy Volunteers
NCT02125578
ATP Expression in Lymphocytes of MS Patients by Means of "ImmuKnow®" Assay.
NCT00618267
An Open-Label, 18FDG-PET Pharmacodynamic Assessment of the Effect of BIIB021 in Subjects With Gastrointestinal Stromal Tumors (GIST)
NCT00618319
Once or Twice Daily Administration of BIIB021 to Subjects With Advanced Solid Tumors
NCT00618735
Evaluation of Safety and Efficacy of Fludarabine, Cyclophosphamide, and Rituximab (FCR) +/- Lumiliximab in Subjects With Previously Untreated Chronic Lymphocytic Leukemia (CLL)
NCT00801060
The Effects of Tysabri Treatment on Vaccination Response and Lymphocyte Subsets in Subjects With Relapsing Forms of Multiple Sclerosis
NCT00536120
Phase 1 Study of BIIB022 (Anti-IGF-1R Monoclonal Antibody) in Relapsed/Refractory Solid Tumors
NCT00555724
CNF2024 (BIIB021) HER2- (QD) HER2+ (BIW w/Herceptin) PK/PD Study
NCT00412412
RTA 744 in Breast Cancer Patients With Progression of Previously Irradiated Brain Metastases
NCT00538343
Safety Study of Natalizumab to Treat Multiple Sclerosis (MS)
NCT00559702
Study With Gemcitabine and RTA 402 for Patients With Unresectable Pancreatic Cancer
NCT00529113
Evaluation of Natalizumab for thE Relief of MS Associated FatiGue
NCT00464074
BG9924 in Combination With Methotrexate Extension of Study 104RA203 (NCT 00458861)
NCT00523328
Efficacy and Safety Study of Oral BG00012 With Active Reference in Relapsing-Remitting Multiple Sclerosis
NCT00451451
Study to Assess the Safety, Tolerability, and Pharmacodynamics of RTA 402 in Patients With Hepatic Dysfunction
NCT00550849
Avonex 15 Year Long Term Follow-up Study
NCT00525343
BG9924 in Combination With Methotrexate for Participants With Active Rheumatoid Arthritis
NCT00458861
Efficacy and Safety of Oral BG00012 in Relapsing-Remitting Multiple Sclerosis
NCT00420212
Pregnancy Exposure Registry for Tysabri®
NCT00472992
TYSABRI Global Observational Program in Safety
NCT00477113
A Multicenter Study to Assess the Effect of Plasma Exchange in Accelerating the Clearance of Natalizumab in Subjects With Multiple Sclerosis (MS)
NCT00424788
Lumiliximab With Fludarabine, Cyclophosphamide, and Rituximab (FCR) Versus FCR Alone in Subjects With Relapsed Chronic Lymphocytic Leukemia (CLL)
NCT00391066
A Safety Study of RTA 744 in Recurrent, Progressive or Refractory Neoplastic Meningitis
NCT00527410
Natalizumab High Titer Immunogenicity and Safety
NCT00516893
Safety and Tolerability of Rituxan With Methotrexate and Etanercept or Methotrexate and Adalimumab in Patients With Active Rheumatoid Arthritis
NCT00298272
Phase Distribution
| Phase | Trial count |
|---|---|
| Phase 1 | 135 |
| Phase 2 | 63 |
| Phase 3 | 71 |
| Phase 4 | 13 |
What the Pipeline for Biogen Shows
According to the ClinicalTrials.gov registry, Biogen is linked to 334 US clinical trials across every stage of research activity. Of those, 21 studies are currently recruiting, about 6% of the sponsor's indexed portfolio, and 237 are already marked complete, representing roughly 71% of the total.
The phase mix for Biogen reports 84 late-stage studies (Phase 3 and Phase 4 combined) and 198 earlier-phase studies (Phase 1 and Phase 2).
The top therapeutic focus area indexed for Biogen is Multiple Sclerosis with 13 linked trials, and 9 other condition areas appear in the top list above.
How to read these pipeline numbers
Recruiting share is one of the more practical signals here: it reflects how much of a sponsor's research is presently open to new participants, while the completed share indicates the depth of finished work that has already contributed registry results. Both counts come directly from the public ClinicalTrials.gov dataset and are refreshed on the registry side; this page mirrors the latest data pull without altering it.
A portfolio weighted toward Phase 3 usually reflects an organization advancing candidates toward regulatory review, where the research centers on comparative efficacy and broader safety across larger populations. A heavier Phase 1 and Phase 2 tilt generally indicates exploratory work, safety, dosing, and early signal detection, and is common among research-forward sponsors that seed many early programs. Phase 4 entries, when present, track interventions already in real-world use and typically focus on long-term safety, effectiveness across subgroups, or formulation comparisons.
That distribution is a quick read of where the organization concentrates its research attention; it does not imply product availability, market share, or any clinical endorsement. All numbers on this page come from ClinicalTrials.gov maintained by the National Library of Medicine, and counts can shift as new studies are registered or existing ones update their status. This information is provided for reference and educational purposes only, not as medical, investment, or regulatory advice, verify current details directly with ClinicalTrials.gov before relying on any figure here.
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page aggregates every registered trial from this sponsor, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.