UCB Pharma

Closed portfolio with a later-stage archive tilt

According to ClinicalTrials.gov-derived indexes, UCB Pharma sits in the top decile of US sponsors by registered trial count (#240 of 15,742 sponsors by registered trial count).

100 total trials none currently recruiting 90 completed later-stage tilt top decile by trial count

UCB Pharma: 100 sponsored US clinical trials, none currently recruiting.

UCB Pharma sponsors 100 registered US clinical trials on ClinicalTrials.gov, none currently recruiting, and 90 completed. 66 of these trials are in Phase 3-4 (later-stage) and 28 in Phase 1-2 (earlier-stage). The most-studied condition in this pipeline is Partial Epilepsies, with 2 trials.

Top-decile sponsor footprint

UCB Pharma ranks in the top decile of sponsors by registered trial count (#240 of 15,742 sponsors by registered trial count). Volume at this scale usually reflects a long institutional pipeline, read phase tilt and therapeutic areas below before treating it as current-year activity.

Trial completion reliability score

C 65/100

90 of 100 decided trials (Completed vs. Terminated on ClinicalTrials.gov) reached their planned completion (90.0%), vs. national p10 68.4% / p90 100% among 1,234 sponsors with at least 10 decided trials. Still-open trials (Recruiting, Active-not-recruiting, Not-yet-recruiting) are excluded since they have not reached an outcome yet.

Indexed trials (enrollment closed)

100 total, page 2 of 2

COMPLETED Phase 3

Conversion to Monotherapy Study With Keppra XR for Partial Seizures

NCT00419094

COMPLETED Phase 3

Trial to Assess Parkinson's Disease (PD) Symptom Control to Four Doses of Rotigotine in a Transdermal Patch

NCT00522379

TERMINATED Phase 3

Long-term Extension of RECOVER- Long-term Effect of the 24h Transdermal Delivery of Rotigotine in Subjects With Idiopathic Parkinson's Disease

NCT00519532

COMPLETED Phase 3

Randomized Evaluation of the 24-Hour Coverage: Efficacy of Rotigotine

NCT00474058

TERMINATED Phase 2

Placebo Controlled Study in Subjects With Relapsing Forms of MS to Evaluate the Safety, Tolerability and Effects of CDP323

NCT00484536

COMPLETED Phase 2

The Use of Rotigotine for Treatment of Reducing Signs and Symptoms of Fibromyalgia in Adults.

NCT00464737

COMPLETED

Evaluation of Treatment Satisfaction in Children With an Allergy and Who Received an Antihistamine

NCT00453583

COMPLETED Phase 2

A Study Designed to Test the Effectiveness and Safety of Treating Patients With Lacosamide for Migraine Prophylaxis

NCT00440518

COMPLETED Phase 3

Examining the Long Term Safety, Efficacy, and Corticosteroid-sparing Effect of Certolizumab Pegol in Crohn's Disease

NCT00356408

COMPLETED Phase 3

Brivaracetam as add-on Treatment of Unverricht-Lundborg Disease (ULD) in Adolescents and Adults

NCT00368251

TERMINATED Phase 3

Corticosteroid Sparing Effect of Certolizumab in Crohn's Disease

NCT00349752

COMPLETED Phase 2

Assessing Efficacy and Safety of Lacosamide Compared to Placebo in Reducing Signs and Symptoms of Fibromyalgia Syndrome.

NCT00401830

COMPLETED Phase 3

Follow-up to Welcome Study C87042 [NCT00308581] Examining Certolizumab Pegol (CDP870) in Subjects With Crohn's Disease

NCT00333788

COMPLETED Phase 2

Study of Epratuzumab in Systemic Lupus Erythematosus

NCT00383513

COMPLETED Phase 3

Certolizumab in Crohn's Disease Patients With Loss of Response or Intolerance to Infliximab

NCT00308581

COMPLETED Phase 3

An Extension Trial to Investigate Long-Term Treatment With Transdermal Rotigotine in Idiopathic Restless Legs Syndrome

NCT00263068

COMPLETED Phase 2

A Dose-ranging Study With Brivaracetam in Patients From 16 to 65 Years With Refractory Partial Onset Seizures.

NCT00175825

COMPLETED Phase 3

A Study of the Safety and Effectiveness of Liquid Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis

NCT00160641

COMPLETED Phase 4

Trial to Compare Time to Response in the Symptoms of Anxiety to Concomitant Treatment With Niravam™ and an SSRI or SNRI to Treatment With an SSRI or SNRI Alone in Subjects With Generalized Anxiety Disorder or Panic Disorder

NCT00266409

COMPLETED Phase 3

Follow-up Trial to Evaluate Long-term Safety and Efficacy of Brivaracetam in Subjects Suffering From Epilepsy

NCT00175916

COMPLETED Phase 2

Study With Subjects 18-65 Years Old With Partial Onset Seizures Who Are Currently Taking Levetiracetam

NCT00152503

COMPLETED Phase 3

A Study of Liquid Certolizumab Pegol as Additional Medication to Methotrexate in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis

NCT00160602

COMPLETED NA

A Randomized, Open-label, Two-way Crossover Trial to Determine the Pharmacokinetics of Metoclopramide When Administered as the Orally Disintegrating Tablet Compared to Reglan® Tablets in Subjects With Diabetic Gastroparesis

NCT00139893

COMPLETED Phase 3

A Study of the Safety and Effectiveness of Lyophilized Certolizumab Pegol in the Treatment of Signs and Symptoms of Rheumatoid Arthritis and in Prevention of Joint Damage in Patients With Active Rheumatoid Arthritis

NCT00175877

COMPLETED Phase 3

A Single Center, Randomized, Double-blind, Crossover Pilot Trial Comparing the Onset of Action of Parcopa™ With Sinemet® in Subjects With Stable Parkinson's Disease

NCT00139880

TERMINATED Phase 3

Study of Epratuzumab in Systemic Lupus Erythematosus

NCT00111306

COMPLETED Phase 3

Four Different Transdermal Doses of Rotigotine in Subjects With Idiopathic Restless Legs Syndrome

NCT00135993

TERMINATED Phase 3

Study of Epratuzumab in Systemic Lupus Erythematosus (SLE)

NCT00383214

COMPLETED Phase 1

An Open-Label Interaction Study to Look at the Effects of Brivaracetam on Phenytoin When Taken Together in 15 Adult Patients With Epilepsy.

NCT00426673

TERMINATED Phase 2

Pharmacokinetics Study of Epratuzumab in Systemic Lupus Erythematosus (SLE)

NCT00113971

COMPLETED Phase 3

An Open-Label Extension Trial to Assess the Safety and Tolerability of Long Term Treatment of Rotigotine in Subjects With Idiopathic Parkinson's Disease

NCT00505687

COMPLETED Phase 2

Safety and Tolerability of Intravenous SPM 927 as Replacement for Oral SPM 927 in Subjects With Partial Seizures

NCT00151879

COMPLETED Phase 3

A Placebo Controlled Study to Assess Efficacy and Safety of Certolizumab Pegol in the Treatment of Rheumatoid Arthritis

NCT00152386

COMPLETED Phase 3

A Multicenter, Open-label Randomized Crossover Trial to Assess Subject Preference for Kemstro™ Compared to Conventional Baclofen Tablets in Subjects With Stable Multiple Sclerosis

NCT00139789

COMPLETED

UCB Antiepileptic Drugs (AED) Pregnancy Registry (Formerly the Keppra® Pregnancy Registry)

NCT00345475

COMPLETED Phase 3

A Trial To Assess Switching From Ropinirole, Pramipexole Or Cabergoline To The Rotigotine Transdermal System In Idiopathic Parkinson's Disease

NCT00242008

COMPLETED Phase 3

Trial to Assess the Efficacy and Safety of SPM 927 (200, 400, and 600mg/Day) in Subjects With Painful Distal Diabetic Neuropathy

NCT00135109

COMPLETED Phase 3

A Placebo-controlled Study of Levetiracetam In Children (1mo to 4yrs of Age) With Partial Onset Seizures.

NCT00175890

COMPLETED Phase 3

Long-Term, Follow-Up Study Of the Safety And Efficacy Of Levetiracetam In Children With Partial Onset Seizures

NCT00152516

COMPLETED Phase 2

A 19-week Cognition Study of Levetiracetam in Children With Partial Onset Seizures

NCT00105040

COMPLETED Phase 2

A Follow-On Trial to Assess the Long Term Safety and Efficacy of SPM 927 in Painful Distal Diabetic Neuropathy

NCT00235443

COMPLETED Phase 3

A Multicenter, Open-Label, Randomized Crossover Trial to Assess Subject Preference for Alprazolam Orally Disintegrating Tablets Compared to Conventional Alprazolam Tablets in Subjects With Anxiety

NCT00139854

COMPLETED Phase 3

A follow-on Safety Study of CDP870 in Subjects With Crohn's Disease (CD) Who Have Completed a 26-week Double Blind Study CDP870-031 [NCT00152490] or CDP870-032 [NCT00152425]

NCT00160524

COMPLETED Phase 2

A Trial to Assess the Efficacy and Safety of SPM 927 in Subjects With Painful Distal Diabetic Neuropathy

NCT00235469

COMPLETED Phase 3

A follow-on Safety Study in Subjects With Crohn's Disease Who Have Previously Been Withdrawn From the Double-blind Study CDP870-031 [NCT00152490] or CDP870-032 [NCT00152425] Due to an Exacerbation of Crohn's Disease

NCT00160706

COMPLETED Phase 3

A Multicenter, Open-label Trial to Assess Subject Preference of PARCOPA, Carbidopa/Levodopa Orally Disintegrating Tablets, Compared to Conventional Carbidopa/Levodopa Tablets in Subjects With Stable Parkinson's Disease

NCT00139867

COMPLETED Phase 3

Open Label Long-Term Safety Study of Certolizumab Pegol (CZP) for Patients With Rheumatoid Arthritis

NCT00160693

COMPLETED Phase 3

An Open-Label Extension Trial to Assess the Safety of Long-Term Treatment of Rotigotine in Advance-Stage Parkinson's Disease

NCT00594386

COMPLETED Phase 3

An Open-Label Extension Trial to Assess the Safety of Long-Term Treatment of Rotigotine in Early-Stage Parkinson's Disease.

NCT00594165

COMPLETED Phase 2

To Determine Tolerability and Efficacy of Long-term Oral Lacosamide in Patients With Partial Seizures

NCT00552305

← Previous Page 2 of 2

How the UCB Pharma archive is shaped

100 indexed studies, none listed as recruiting (0% open); 90 completed (90%).

Phase mix: 66 late (III/IV) vs 28 early (I/II) (later-stage heavy).

Top condition: Partial Epilepsies (2 trials), 9 others listed.

How to read a closed sponsor archive

When recruiting_count is zero, the indexed set is completed or otherwise not open. Phase tilt still describes where archived studies sat on the investigational pathway. Re-check ClinicalTrials.gov before acting.

UCB Pharma: archived-pipeline peers nationwide

Peers matched on 100 indexed studies with no current recruiting: volume and archive shape, not condition overlap.

UCB Pharma sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot). 2×2 strategic matrix plotting 9 entities by Total trials (X) and Recruiting share (Y), with a crosshair dividing the plot into four quadrants. Higher volume & more openFocused & more openHigher volume, mostly closedSmaller & mostly closed 050100150 0%5%10%15%20% Total trials Recruiting share UCB PharmaWake Forest UniversitySpaulding Rehabilitation HospitalGE HealthcareJohnson & Johnson Pharmaceutical Research & Development, L.L.C.10xBio22nd Century Group23andMe3-C Institute for Social Development
UCB Pharma sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together. Source: ClinicalTrials.gov (2026-08-08 snapshot).

UCB Pharma sits at or above the median trial volume and at or above the median recruiting share among these 9 nationwide peers -- the two do not always move together.

Sponsors near 100 archived trials

Sponsors with similar archive density (± trial count)

What to do with this UCB Pharma page

100 registered trials is a research-attention snapshot, not an endorsement of UCB Pharma or any single study.

  • None of UCB Pharma's trials are currently recruiting in this registry; that can change as new trials post, or check the broader research index. Browse research indexes
  • Partial Epilepsies is the condition UCB Pharma studies most, compare against other sponsors active in the same condition before evaluating a specific study. See Partial Epilepsies trials
  • Bring the specific trial ID (NCT number) to your own doctor before enrolling, this page is a directory, not medical guidance. Read the trial-finding guide

Trial and recruiting counts reflect ClinicalTrials.gov registry status as of the data vintage above; individual trial eligibility and enrollment status can change.

UCB Pharma pipeline card: 100 registered trials from official public datasets.Report a data error.