Brussels, Belgium, Belgium · Est. 1868 · 8,000 employees
UCB is a biopharmaceutical company focused on discovering and developing innovative medicines in immunology and neurology.
Pipeline Programs↗
Distinct drugs in development (Preclinical–Phase 3)
Indications↗
Distinct diseases across all programs
Clinical Trials↗
All sponsored trials (all statuses)
Orange Book Patents
Across 6 drugs with upcoming expirations
Pipeline
By Phase
7 drugs in development
By Therapeutic Area
top 2
R&D Momentum
65/100
Pipeline Velocity
39/100
Trial Completion Rate
88/100
Pipeline Concentration
63/100
Pipeline Freshness
80/100
Strategic Signals
Activity
Last 14 days
A Phase 3 Randomized, Double-Blind, Placebo Controlled, Parallel Group, Multicenter Study With Open-Label Extension to Evaluate the Efficacy And Safety of Fenfluramine Hydrochloride in Study Participants With Rett Syndrome
A Multicenter, Randomized, Parallel-Group, Double-Blind, Active-Controlled Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Ustekinumab in Children and Adolescents From 6 Years to Less Than 18 Years of Age With Moderate to Severe Plaque Psoriasis
A Multicenter, Open-Label Extension Study to Assess the Long-Term Safety and Tolerability of Dapirolizumab Pegol Treatment in Study Participants With Systemic Lupus Erythematosus
A Multicenter Open-label, Prospective Study to Assess the Concentration of Bimekizumab in Mature Breast Milk From Mothers Receiving Treatment With Bimzelx® (Bimekizumab)
Open-Label, Single-Arm, Phase 3 Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Fenfluramine (Hydrochloride) in Infants 1 Year to Less Than 2 Years of Age With Dravet Syndrome
A First-in-Human, Randomized, Investigator-Blind, Participant-Blind, Placebo-Controlled Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single Ascending Doses of UCB3101 in Healthy Participants
A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled Study of 24 to 52 Weeks Treatment to Evaluate The Efficacy And Safety of Galvokimig in Study Participants With Moderate-to-Severe Chronic Obstructive Pulmonary Disease With Chronic Bronchitis (SCALA)
An Open-label, Single-arm Study Evaluating the Activity, Safety, and Pharmacokinetics of Rozanolixizumab in Pediatric Study Participants With Moderate to Severe Generalized Myasthenia Gravis
A Double-Blind, Randomized, Placebo-Controlled, Multicenter, Outpatient, Parallel-Group Study to Assess the Efficacy and Safety of Staccato Alprazolam in Study Participants 12 Years of Age and Older With Stereotypical Prolonged Seizures
A Phase 2, Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group Study of 24 to 52 Weeks Treatment to Evaluate The Efficacy And Safety of Galvokimig in Adult Study Participants With Non-Cystic Fibrosis Bronchiectasis (ATMOS)
A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Dose-Ranging Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Galvokimig in Adult Study Participants With Moderate to Severe Atopic Dermatitis
A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Ocular Myasthenia Gravis
Details
Company Overview
$20.0B
Mkt Cap
$5.3B
Revenue
—
Cash
Therapeutic Focus
Pipeline
Regulatory
Vimpat — VIMPAT
Application NDA022253 (NDA)
Vimpat — VIMPAT
Application NDA022255 (NDA)
Keppra — LEVETIRACETAM IN SODIUM CHLORIDE
Application NDA202543 (NDA)
Neupro — NEUPRO
Application NDA021829 (NDA)
Keppra — SPRITAM
Application NDA207958 (NDA)
Briviact — BRIVIACT
Application NDA205837 (NDA)
Briviact — BRIVIACT
Application NDA205838 (NDA)
Briviact — BRIVIACT
Application NDA205836 (NDA)
Keppra — ELEPSIA XR
Application NDA204417 (NDA)
Fintepla — FINTEPLA
Application NDA212102 (NDA)
Zilbrysq — ZILBRYSQ
Application NDA216834 (NDA)
Bimzelx — BIMZELX
Application BLA761151
Bimzelx — BIMZELX
Application BLA761151 (BLA)
Rysodeg — RYSTIGGO
Application BLA761286 (BLA)
Vimpat — MOTPOLY XR
Application NDA216185 (NDA)
Bimzelx — BIMZELX
Application BLA761151
Bimzelx — BIMZELX
Application BLA761151
Bimzelx — BIMZELX
Application BLA761151
Bimzelx — BIMZELX
Application BLA761151
Bimzelx — BIMZELX
Application BLA761151
Data sources: ClinicalTrials.gov (NIH) · OpenFDA (FDA) · ChEMBL (EMBL-EBI) · Open Targets (EBI/Sanger) · MedlinePlus (NIH) · PubMed (NIH) · SEC EDGAR (SEC)