UCB Cares
001 844 599 2273 · 001 844 599 2273 (UCB) · 0018445992273
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Trials
Studies that name UCB Cares as principal investigator, study chair or study director, newest first. Live from ClinicalTrials.gov, fetched 2026-11-11 23:55 UTC. Showing 200 of 236. Open this list on ClinicalTrials.gov
- Ph1NCT07849894 · A Study to Evaluate the Safety, Pharmacokinetics and Pharmacodynamics of UCB0159 in Participants With Mild to Moderate Psoriasis, Single Dose Pharmacokinetics and Safety in Healthy Participants.UCB Biopharma SRL · completed · Mild to Moderate Psoriasis, Healthy Volunteers · study director
- N/ANCT07531511 · SLC6A1-NDD Prospective Longitudinal Natural History StudyUCB Biopharma SRL · recruiting · SLC6A1 Neurodevelopmental Disorder (NDD), Developmental and Epileptic Encephalopathies (DEE) · study director
- Ph3NCT07503444 · A Phase 3 Study of Fenfluramine Hydrochloride in Rett SyndromeUCB BIOSCIENCES, Inc. · recruiting · Rett Syndrome · study director
- Ph1NCT07290036 · A Study to Learn if Bimekizumab Given in Different Ways is Safe and Moves Similarly Throughout the Body Over Time in AdultsUCB Biopharma SRL · recruiting · Psoriatic Arthritis, Axial Spondyloarthritis · study director
- Ph1NCT07286682 · A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of UCB5285 in Healthy Study ParticipantsUCB Biopharma SRL · active not recruiting · Healthy Participants · study director
- Ph2NCT07277660 · A Dose-ranging Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Galvokimig in Adult Study Participants With Atopic DermatitisUCB Biopharma SRL · active not recruiting · Atopic Dermatitis · study director
- Ph4NCT07246564 · Phase 4 Study Evaluating Efficacy and Safety of Rozanolixizumab in Adult Chinese Participants With Generalized Myasthenia GravisUCB Biopharma SRL · active not recruiting · Myasthenia Gravis · study director
- Ph1NCT07220551 · A Phase 1 Relative Bioavailability Study of UCB0022 Tablets in Healthy ParticipantsUCB Biopharma SRL · completed · Healthy Volunteers · study director
- Ph3NCT07219420 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Palmoplantar PustulosisUCB Biopharma SRL · recruiting · Palmoplantar Pustulosis · study director
- Ph1NCT07020988 · A Study to Assess the Time to Onset of Action of Staccato Alprazolam Versus Midazolam and Diazepam in Healthy ParticipantsUCB Biopharma SRL · completed · Healthy Participants · study director
- Ph1NCT06970301 · A Study to Assess the Safety and Tolerability, and Pharmacokinetics of UCB0022 in Healthy Caucasian, Japanese, and Chinese ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph1NCT06961747 · A Study to Assess Zilucoplan Concentration in Breast Milk of Healthy Lactating WomenUCB Biopharma SRL · recruiting · Healthy Participants · study director
- Ph3NCT06921850 · A Study to Assess the Pharmacokinetics and Safety of Bimekizumab in Children and Adolescents With Moderate to Severe Hidradenitis SuppurativaUCB Biopharma SRL · active not recruiting · Hidradenitis Suppurativa · study director
- Ph1NCT06888193 · A Study to Assess the Concentration of Bimekizumab in Mature Breast Milk From Mothers Receiving Treatment With Bimzelx® (Bimekizumab)UCB Biopharma SRL · recruiting · Moderate to Severe Plaque Psoriasis, Psoriatic Arthritis, Axial Spondyloarthritis · study director
- Ph1NCT06720714 · A Study to Assess the Concentration of Rozanolixizumab in the Breast Milk of Healthy Lactating WomenUCB Biopharma SRL · completed · Healthy Participants · study director
- Ph1NCT06716879 · A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of a Single Dose of Donzakimig in Healthy Chinese and Japanese ParticipantsUCB Biopharma SRL · completed · Healthy Participants · study director
- Ph1NCT06679413 · A Study to Assess Drug-drug Interaction of ZX008 in Healthy Male and Female Study ParticipantsUCB BIOSCIENCES, Inc. · completed · Healthy Study Participants · study director
- Ph3NCT06668181 · An Open-label Study to Evaluate the Pharmacokinetics and Safety of Bimekizumab in Pediatric Study Participants With Active Juvenile Idiopathic Arthritis Subtypes Enthesitis-related Arthritis (Including Juvenile-onset Ankylosing Spondylitis) and Juvenile Psoriatic ArthritisUCB Biopharma SRL · recruiting · Enthesitis-related Arthritis, Juvenile Psoriatic Arthritis · study director
- Ph3NCT06624228 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Study Participants With Active Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph3NCT06617325 · A Study to Evaluate the Efficacy and Safety of Dapirolizumab Pegol in Study Participants With Moderately to Severely Active Systemic Lupus ErythematosusUCB Biopharma SRL · recruiting · Systemic Lupus Erythematosus · study director
- N/ANCT06590493 · Doxecitine and Doxribtimine-Expanded AccessUCB BIOSCIENCES, Inc. · available · Thymine Kinase 2 Deficiency · study director
- Ph1NCT06555601 · A First-in-human Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of UCB3101 in Healthy ParticipantsUCB Biopharma SRL · terminated · Healthy Participants · study director
- Ph3NCT06540144 · An Extension Study Evaluating 6-week Treatment Cycles of Rozanolixizumab in Pediatric Study Participants With Generalized Myasthenia GravisUCB Biopharma SRL · active not recruiting · Generalized Myasthenia Gravis · study director
- Ph1NCT06511076 · A Study to Evaluate Zilucoplan Injected Subcutaneously Either by a Prefilled Syringe or an Auto-injector in Healthy Adult ParticipantsUCB Biopharma SRL · completed · Healthy Volunteers · study director
- Ph3NCT06506916 · A Study to Evaluate the Effect of Bimekizumab on Gene Expression Biomarkers in Study Participants With Moderate to Severe Plaque PsoriasisUCB Biopharma SRL · active not recruiting · Moderate to Severe Plaque Psoriasis, Psoriatic Arthritis · study director
- Ph3NCT06471361 · A Study to Evaluate the Safe and Effective Use of a Zilucoplan Auto-injector by Study Participants With Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT06435312 · An Open-label Extension Study to Evaluate Subcutaneous Zilucoplan in Pediatric Participants With Generalized Myasthenia GravisUCB Biopharma SRL · enrolling by invitation · Generalized Myasthenia Gravis · study director
- Ph3NCT06425549 · A 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 PsoriasisUCB Biopharma SRL · active not recruiting · Moderate to Severe Plaque Psoriasis · study director
- Ph1NCT06312566 · A Study to Assess the Bioequivalence Between Brivaracetam Tablet and Dry Syrup in Healthy Japanese Male Study ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph2/Ph3NCT06149559 · A Study of Rozanolixizumab in Pediatric Study Participants With Moderate to Severe Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT06118255 · A Study to Evaluate Safety, Tolerability, and Pharmacokinetics of Fenfluramine (Hydrochloride) in Infants 1 Year to Less Than 2 Years of Age With Dravet SyndromeUCB BIOSCIENCES, Inc. · completed · Dravet Syndrome · study director
- Ph2/Ph3NCT06055959 · A Study to Evaluate Subcutaneous Zilucoplan in Pediatric Participants With Generalized Myasthenia GravisUCB Biopharma SRL · recruiting · Generalized Myasthenia Gravis · study director
- Ph2NCT06055985 · A Study to Evaluate the Efficacy, Safety, Tolerability, and Pharmacokinetics of UCB0022 in Study Participants With Advanced Parkinson's DiseaseUCB Biopharma SRL · completed · Parkinson Disease · study director
- Ph3NCT06011733 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Chinese Adult Study Participants With Moderate to Severe Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis · study director
- Ph1NCT05845645 · A Study to Test Bioavailability of of 2 New Formulations of UCB0599 in Healthy Participants in Part A and to Test Safety, Tolerability, and Pharmacokinetic (PK) of UCB0599 in Healthy Japanese and Chinese Participants in Part BUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph3NCT05681715 · A Phase 3, Open-label, Crossover Study to Evaluate Self-administration of Rozanolixizumab by Study Participants With Generalized Myasthenia Gravis (gMG)UCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph2NCT05643794 · A Proof-of-concept Study to Evaluate the Efficacy and Safety of Rozanolixizumab to Treat Adult Study Participants With Severe Fibromyalgia SyndromeUCB Biopharma SRL · completed · Fibromyalgia · study director
- Ph1NCT05626439 · A Relative Bioavailability Study of Staccato Alprazolam Versus Oral Alprazolam in Healthy Study ParticipantsUCB Biopharma SRL · completed · Healthy Participants · study director
- Ph2NCT05543252 · An Extension Study to Evaluate the Long-Term Efficacy, Safety and Tolerability of Minzasolmin (UCB0599) in Study Participants With Parkinson's DiseaseUCB Biopharma SRL · terminated · Parkinson's Disease · study director
- Ph3NCT05514873 · An Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of Subcutaneous Zilucoplan in Participants With Generalized Myasthenia Gravis Who Were Previously Receiving Intravenous Complement Component 5 InhibitorsUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph1NCT05315947 · A Study to Assess the Bioequivalence Between Brivaracetam Tablet and Dry Syrup in Healthy Male Japanese Study ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph1NCT05292131 · A Bioequivalence Study of Bimekizumab Given as 1x2mL or 2x1mL Subcutaneous Injection Using an Autoinjector in Healthy Study ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph1/Ph2NCT05277571 · A Single-ascending Dose (Part A) and Repeat-dose (Part B) Study to Investigate the Safety, Pharmacokinetics and Efficacy (Part B Only) of UCB1381 in Healthy Study Participants (Part A) and in Study Participants With Moderate to Severe Atopic Dermatitis (Part B)UCB Biopharma SRL · completed · Atopic Dermatitis · study director
- Ph3NCT05109234 · A Study to Test the Long-term Safety, Tolerability and Efficacy of Brivaracetam in Study Participants 2 to 26 Years of Age With Childhood Absence Epilepsy or Juvenile Absence EpilepsyUCB Biopharma SRL · completed · Childhood Absence Epilepsy, Juvenile Absence Epilepsy · study director
- Ph3NCT05077904 · A Study to Test the Efficacy and Safety of Staccato Alprazolam in Study Participants 12 Years of Age and Older With Stereotypical Prolonged SeizuresUCB Biopharma SRL · recruiting · Stereotypical Prolonged Seizures · study director
- Ph3NCT05076617 · A Study to Test the Safety and Tolerability of Staccato Alprazolam in Study Participants 12 Years of Age and Older With Stereotypical Prolonged SeizuresUCB Biopharma SRL · enrolling by invitation · Stereotypical Prolonged Seizures · study director
- Ph3NCT05067335 · A Study to Test the Efficacy, Safety and Tolerability of Romosozumab Treatment in Postmenopausal Chinese Women With OsteoporosisUCB Biopharma SRL · completed · Osteoporosis · study director
- Ph3NCT05064878 · A Phase 3 Study to Examine the Efficacy and Safety of ZX008 in Subjects With CDKL5 Deficiency Disorder.Zogenix, Inc. · active not recruiting · CDKL5 Deficiency Disorder, Generalized Tonic Clonic Seizure, Epileptic Spasm · study director
- Ph3NCT05063162 · A Study to Evaluate the Efficacy and Safety of Rozanolixizumab in Adult Participants With Myelin Oligodendrocyte Glycoprotein (MOG) Antibody-associated Disease (MOGAD)UCB Biopharma SRL · active not recruiting · Myelin Oligodendrocyte Glycoprotein Antibody-associated Disease (MOGAD) · study director
- Ph1NCT05028127 · A Study to Evaluate the Relative Bioavailability and Tolerability of Bimekizumab in Healthy SubjectsUCB Celltech · completed · Healthy Volunteers · study director
- Ph3NCT05020249 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Korean Study Participants With Moderate to Severe Plaque PsoriasisUCB Biopharma SRL · completed · Moderate to Severe Plaque Psoriasis · study director
- N/ANCT05017818 · A Retrospective Study of Subjects With Thymidine Kinase 2 DeficiencyZogenix MDS, Inc. · completed · Thymidine Kinase 2 Deficiency · study director
- N/ANCT05014724 · CIDP07 Rozanolixizumab Post Trial Access Program (the PTA)UCB Biopharma SRL · no longer available · Chronic Inflammatory Demyelinating Polyneuropathy (CIDP) · study director
- Ph3NCT04976322 · A Study to Evaluate the Safety and Tolerability of Dapirolizumab Pegol in Study Participants With Systemic Lupus ErythematosusUCB Biopharma SRL · enrolling by invitation · Systemic Lupus Erythematosus · study director
- Ph3NCT04901195 · A Study to Test the Long-term Treatment of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis SuppurativaUCB Biopharma SRL · completed · Hidradenitis Suppurativa · study director
- Ph1NCT04882540 · A Study to Evaluate the Pharmacokinetics and Safety of Brivaracetam in Healthy Chinese SubjectsUCB Biopharma SRL · completed · Healthy Participants · study director
- Ph2NCT04875975 · A Study to Test the Efficacy, Safety, and Pharmacokinetics of Rozanolixizumab in Adult Study Participants With Leucine-Rich Glioma Inactivated 1 Autoimmune EncephalitisUCB Biopharma SRL · terminated · Leucine-Rich Glioma Inactivated 1 Autoimmune Encephalitis · study director
- Ph1NCT04875962 · A Study to Test the Safety, Tolerability, and Pharmacokinetics of UCB0599 in Healthy Study Participants and Patients With Parkinson's Disease (PD)UCB Biopharma S.P.R.L. · completed · Parkinson's Disease · study director
- Ph1NCT04867642 · A Study to Test the Safety, Tolerability, and Blood Levels of UCB0022 in Healthy Participants and Participants With Parkinson's DiseaseUCB Biopharma SRL · completed · Healthy Study Participants, Parkinson's Disease · study director
- Ph2NCT04867616 · A Study to Test the Efficacy, Safety, and Tolerability of Bepranemab (UCB0107) in Patients With Mild Cognitive Impairment or Mild Alzheimer's Disease (AD)UCB Biopharma SRL · completed · Alzheimer's Disease · study director
- Ph1NCT04857307 · A Study to Assess the Pharmacokinetics (PK) and Safety of Staccato Alprazolam in Adolescent Study Participants With EpilepsyUCB Biopharma SRL · completed · Epilepsy · study director
- Ph1NCT04828343 · A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Rozanolixizumab Administered Subcutaneously Via Manual Push Versus Syringe Driver to Healthy ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph1NCT04802746 · A Study to Assess the Pulmonary Safety of Staccato Alprazolam in Healthy Study Participants and in Study Participants With Mild AsthmaUCB Biopharma SRL · completed · Healthy Study Participants, Participants With Mild Asthma · study director
- Ph1NCT04782388 · Study to Assess the Safety, Tolerability, And Pharmacokinetics of Staccato Alprazolam in Healthy Japanese, Chinese, and Caucasian ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · study director
- Ph1NCT04740814 · A Study to Assess the Pharmacokinetics of Certolizumab Pegol in Adults With Active Rheumatoid ArthritisUCB Biopharma SRL · completed · Rheumatoid Arthritis · study director
- Ph2NCT04718896 · A Study to Assess the Pharmacokinetics, Safety, and Efficacy of Two Doses of Bimekizumab in Adolescent Study Participants With Moderate to Severe Plaque PsoriasisUCB Biopharma SRL · completed · Moderate to Severe Plaque Psoriasis · study director
- Ph3NCT04715646 · A Study to Test the Safety and Tolerability of Brivaracetam in Children and Adolescents With SeizuresUCB Biopharma SRL · recruiting · Epilepsy · study director
- Ph1NCT04705350 · A Study to Test Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Single Ascending Intravenous Doses of Zampilimab in Healthy ParticipantsUCB Biopharma SRL · completed · Healthy Study Participants · principal investigator
- Ph3NCT04666610 · A Study to Evaluate the Efficacy, Safety, and Tolerability of Brivaracetam as Monotherapy in Patients 2 to 25 Years of Age With Childhood Absence Epilepsy or Juvenile Absence EpilepsyUCB Biopharma SRL · completed · Childhood Absence Epilepsy, Juvenile Absence Epilepsy · study director
- Ph1NCT04658199 · A Study to Test the Safety and Tolerability of Long-term UCB0107 Administration in Study Participants With Progressive Supranuclear PalsyUCB Biopharma SRL · active not recruiting · Progressive Supranuclear Palsy · study director
- Ph2NCT04658186 · A 18-month Study to Evaluate the Efficacy, Safety, Tolerability and Pharmacokinetics of Oral UCB0599 in Study Participants With Early-stage Parkinson's DiseaseUCB Biopharma SRL · completed · Early-stage Parkinson's Disease · study director
- Ph3NCT04650854 · A Study to Evaluate Rozanolixizumab in Study Participants With Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph1NCT04651153 · A Safety and Pharmacokinetics Study of UCB7853 in Healthy Study Participants and Study Participants With Parkinson's Disease (PD)UCB Biopharma SRL · completed · Parkinson's Disease · study director
- Ph1/Ph2NCT04643457 · A Study to Test the Safety, Pharmacokinetics, and Efficacy of UCB9741 in Healthy Study Participants and in Study Participants With Atopic DermatitisUCB Biopharma SRL · completed · Atopic Dermatitis · study director
- Ph3NCT04643483 · A Study to Test Efficacy, Safety, and Pharmacokinetics of Certolizumab Pegol in Children and Adolescents With Moderately to Severely Active Crohn's DiseaseUCB Biopharma SRL · withdrawn · Crohn's Disease · study director
- Ph3NCT04627285 · A Study to Test the Long-term Use of Oral Lacosamide in Pediatric Study Participants Who Completed NCT01964560 (EP0034) or NCT00938912 (SP848) and Received Lacosamide TreatmentUCB Biopharma SRL · completed · Epilepsy · study director
- Ph3NCT04596995 · A Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Rozanolixizumab in Study Participants With Persistent or Chronic Primary Immune Thrombocytopenia (ITP)UCB Biopharma SRL · terminated · Primary Immune Thrombocytopenia · study director
- Ph3NCT04581733 · A Study of the Efficacy and Safety of MT1621 in Thymidine Kinase 2 (TK2) Deficiency (Treatment naïve)Zogenix MDS, Inc. · withdrawn · Thymidine Kinase 2 Deficiency · study director
- Ph2NCT04519645 · A Study to Evaluate the Efficacy, Safety, and Pharmacokinetics of Lacosamide in Neonates With Repeated Electroencephalographic Neonatal SeizuresUCB Biopharma SRL · terminated · Electroencephalographic Neonatal Seizures, Epilepsy · study director
- Ph1NCT04444466 · A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of UCB8600 in Healthy Participants, Atopic Participants, and Chronic Spontaneous Urticaria ParticipantsUCB Biopharma SRL · terminated · Healthy Study Participants, Chronic Spontaneous Urticaria · study director
- Ph3NCT04436640 · A Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Subjects With Active Axial Spondyloarthritis Including Ankylosing Spondylitis and Nonradiographic Axial SpondyloarthritisUCB Biopharma SRL · completed · Axial Spondyloarthritis, Ankylosing Spondylitis, r-axSpa · study director
- Ph1/Ph2NCT04393298 · A Study to Assess the Safety, Pharmacokinetics and Anti Tumor Activity of UCB6114 Administered Intravenously to Participants With Advanced Solid TumorsUCB Biopharma SRL · completed · Advanced Solid Tumors · study director
- Ph1/Ph2NCT04335578 · A Study to Evaluate Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Zampilimab in Adult Kidney Transplant Recipients With Chronic Allograft InjuryUCB Biopharma SRL · terminated · Chronic Allograft Injury · principal investigator
- Ph3NCT04294667 · A Study to Evaluate the Efficacy and Safety of Dapirolizumab Pegol in Study Participants With Moderately to Severely Active Systemic Lupus ErythematosusUCB Biopharma SRL · completed · Systemic Lupus Erythematosus · study director
- Ph1NCT04283136 · A Study to Test the Blood Concentration of 4 Padsevonil Product Variants and the Effect of Food on PadsevonilUCB Biopharma SRL · withdrawn · Healthy Participants, Epilepsy · study director
- Ph1NCT04255862 · A Study to Evaluate the Bioequivalence of Bimekizumab Given as 1x2mL or 2x1mL Subcutaneous Injection in Healthy Study ParticipantsUCB Biopharma SRL · terminated · Healthy Study Participants · study director
- Ph3NCT04242446 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis SuppurativaUCB Biopharma SRL · completed · Hidradenitis Suppurativa · study director
- Ph3NCT04242498 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Study Participants With Moderate to Severe Hidradenitis SuppurativaUCB Biopharma SRL · completed · Hidradenitis Suppurativa · study director
- Ph3NCT04225871 · Open-Label Extension of Zilucoplan in Subjects With Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT04224688 · A Study to Assess the Efficacy, Safety, and Tolerability of Rozanolixizumab in Adult Study Participants With Persistent or Chronic Primary Immune Thrombocytopenia (ITP)UCB Biopharma SRL · terminated · Primary Immune Thrombocytopenia · study director
- Ph3NCT04200456 · A Study to Evaluate the Efficacy, Safety, and Tolerability of Rozanolixizumab in Adult Study Participants With Persistent or Chronic Primary Immune Thrombocytopenia (ITP)UCB Biopharma SRL · terminated · Primary Immune Thrombocytopenia · study director
- Ph1NCT04185415 · A Study to Test the Safety and Tolerability of UCB0107 in Study Participants With Progressive Supranuclear Palsy (PSP)UCB Biopharma SRL · completed · Progressive Supranuclear Palsy · study director
- Ph1NCT04163016 · A Study in Pregnant Women With Chronic Inflammatory Diseases Treated With Cimzia (Certolizumab Pegol)UCB Biopharma SRL · completed · Rheumatoid Arthritis, Psoriatic Arthritis, Crohn's Disease · study director
- Ph1NCT04136444 · A Pharmacokinetic Study of Padsevonil in Study Participants With Either Normal or Moderately Impaired Hepatic FunctionUCB Biopharma S.P.R.L. · terminated · Healthy Study Participants, Impaired Hepatic Function · study director
- Ph1NCT04131517 · A Study to Test the Interaction of Padsevonil With Oral Contraceptives in Healthy Female ParticipantsUCB Biopharma SRL · terminated · Healthy Female Participants · study director
- Ph1NCT04126343 · A Study to Test the Cardiac Effects of Padsevonil in Healthy Study ParticipantsUCB Biopharma S.P.R.L. · terminated · Healthy Study Participants · study director
- Ph3NCT04124965 · A Study to Investigate the Long-term Safety, Tolerability, and Efficacy of Rozanolixizumab in Adult Patients With Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT04123795 · A Study to Evaluate the Pharmacokinetics, Safety, and Effectiveness of Certolizumab Pegol in Children With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Moderate Chronic Plaque Psoriasis, Severe Chronic Plaque Psoriasis, Mixed Guttate/Plaque Psoriasis · study director
- Ph3NCT04115293 · Safety, Tolerability, and Efficacy of Zilucoplan in Subjects With Generalized Myasthenia GravisRa Pharmaceuticals, Inc. · completed · Myasthenia Gravis, Generalized · study director
- Ph3NCT04109976 · A Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or the Auto-injector for the Subcutaneous Self-injection of Bimekizumab Solution by Subjects With Active Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph1NCT04075409 · A Study to Test the Safety, and Tolerability of Padsevonil in Healthy Male Japanese Study ParticipantsUCB Biopharma S.P.R.L. · completed · Healthy Japanese Participants · study director
- N/ANCT04053881 · A Study to Assess How Well Certolizumab Pegol Works in Patients With Moderate to Severe Plaque Psoriasis as Part of Routine Clinical PracticeUCB Biopharma SRL · completed · Plaque Psoriasis · study director
- Ph2NCT04051944 · A Study to Assess Long-term Safety, Tolerability and Efficacy of Rozanolixizumab in Subjects With Chronic Inflammatory Demyelinating PolyradiculoneuropathyUCB Biopharma SRL · completed · Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) · study director
- Ph1NCT04039919 · A Study to Test the Pharmacodynamic, Pharmacokinetic, Safety, and Tolerability of Padsevonil in Healthy Study Participants Receiving Either Ethanol or CannabidiolUCB Biopharma S.P.R.L. · terminated · Healthy Participants · study director
- Ph2NCT04025632 · Safety and Efficacy Study of Zilucoplan in Subjects With Immune-Mediated Necrotizing MyopathyRa Pharmaceuticals · terminated · Immune Mediated Necrotizing Myopathy · study director
- Ph1NCT04013191 · A Study to Test the Safety and Tolerability of Single and Multiple Doses of Padsevonil in Adult and Elderly Study ParticipantsUCB Biopharma S.P.R.L. · completed · Elderly Study Participants, Adult Study Participants · study director
- Ph3NCT04009499 · A Study to Assess the Long-term Safety, Tolerability, and Efficacy of Bimekizumab in the Treatment of Subjects With Active Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph3NCT03992196 · A Follow-up Study of Rotigotine Patch in Adolescent Subjects With Restless Legs SyndromeUCB Biopharma SRL · terminated · Restless Legs Syndrome · study director
- Ph3NCT03971422 · A Study to Test Efficacy and Safety of Rozanolixizumab in Adult Patients With Generalized Myasthenia GravisUCB Biopharma SRL · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT03936777 · A Study to Investigate the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride) Oral Solution in Children and Adults With Epileptic Encephalopathy Including Dravet Syndrome and Lennox-Gastaut SyndromeZogenix, Inc. · completed · Dravet Syndrome, Lennox Gastaut Syndrome, Epileptic Encephalopathy · study director
- Ph3NCT03928704 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Nonradiographic Axial SpondyloarthritisUCB Biopharma SRL · completed · Nonradiographic Axial Spondyloarthritis · study director
- Ph3NCT03928743 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Subjects With Active Ankylosing SpondylitisUCB Biopharma SRL · completed · Ankylosing Spondylitis · study director
- Ph3NCT03896581 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph3NCT03895203 · A Study to Test the Efficacy and Safety of Bimekizumab in the Treatment of Subjects With Active Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph1NCT03895385 · A Study to Evaluate the Antibody Response of Influenza Vaccination Following Concomitant Exposure to Bimekizumab in Healthy SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- Ph2NCT03861481 · A Study to Assess the Efficacy, Safety and Tolerability of Rozanolixizumab in Subjects With Chronic Inflammatory Demyelinating PolyradiculoneuropathyUCB Biopharma S.P.R.L. · completed · Chronic Inflammatory Demyelinating Polyradiculoneuropathy (CIDP) · study director
- Ph1NCT03859219 · A Study to Evaluate Safety and Tolerability of Single Ascending Doses of Rozanolixizumab Administered by Subcutaneous Infusion in Healthy Japanese, Chinese and Caucasian Study ParticipantsUCB Biopharma S.P.R.L. · completed · Healthy-volunteers · study director
- Ph2NCT03845712 · An Open-Label Study of Continuation Treatment With Combination Pyrimidine Nucleosides in Patients With TK2 DeficiencyUCB BIOSCIENCES, Inc. · completed · Thymidine Kinase 2 Deficiency · study director
- Ph3NCT03766685 · A Study to Evaluate the Safe and Effective Use of the Prefilled Safety Syringe or the Auto-injector for the Subcutaneous Self-injection of Bimekizumab Solution by Subjects With Moderate to Severe Chronic Plaque Psoriasis (PSO)UCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis · study director
- Ph3NCT03739840 · A Study to Test the Efficacy and Safety of Padsevonil as Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant EpilepsyUCB Biopharma SRL · terminated · Drug-Resistant Epilepsy, Focal-Onset Seizures · study director
- Ph3NCT03728933 · A Study of Rotigotine Patch in Adolescent Subjects With Restless Legs Syndrome of Unknown CauseUCB Biopharma SRL · terminated · Restless Legs Syndrome · study director
- Ph1NCT03707717 · A Study to Compare the Blood Level of Bimekizumab Injected Subcutaneously Either by a Prefilled Syringe or by an Auto-injector in Adult Healthy Volunteer ParticipantsUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- N/ANCT03701568 · A RETROspective Study of Patients With TK2dZogenix MDS, Inc. · completed · Thymidine Kinase 2 (TK2) · study director
- Ph1NCT03695094 · A Study in Participants With Epilepsy, to Evaluate the Pharmacokinetics, Safety and Tolerability of Oxcarbazepine on PadsevonilUCB Biopharma S.P.R.L. · completed · Epilepsy · study director
- Ph3NCT03685630 · A Study to Evaluate the Safety and Tolerability of Intravenous Brivaracetam (BRV) as Replacement for Oral Brivaracetam in Japanese Subjects >=16 Years of Age With Partial Seizures With or Without Secondary GeneralizationUCB Biopharma S.P.R.L. · completed · Partial Seizures With or Without Secondary Generalization, Epilepsy · study director
- Ph1NCT03605082 · A Study to Test the Safety and Tolerability and Pharmacokinetics of Single Doses of UCB0107 in Healthy Japanese SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Japanese Volunteers · study director
- Ph3NCT03598790 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis · study director
- N/ANCT03559660 · CUP Certolizumab Pegol (CDP-870) in Adults Suffering From Crohn's Disease (CD)UCB Biopharma SRL · no longer available · Crohn's Disease · study director
- N/ANCT03559673 · Compassionate Use Program With Lacosamide in Patients With Partial-onset or Generalized Tonic-clonic SeizuresUCB Biopharma S.P.R.L. · no longer available · Epilepsies, Partial · study director
- N/ANCT03559686 · Named Patient Program With Certolizumab Pegol in Adults Suffering From Rheumatoid Aarthritis (RA)UCB Biopharma SRL · no longer available · Rheumatoid Arthritis · study director
- Ph3NCT03536884 · A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis · study director
- N/ANCT03532516 · Compassionate Use Program With Brivaracetam for the Treatment of Patients With EpilepsyUCB Biopharma SRL · no longer available · Epilepsy · study director
- Ph1NCT03480243 · Study to Evaluate the Effect of Coadministered Erythromycin on the Pharmacokinetics and Safety of PadsevonilUCB Biopharma S.P.R.L. · completed · Pharmacokinetics · study director
- Ph1NCT03464227 · A Study to Test the Safety, Pharmacokinetics, and Pharmacodynamics of Single Ascending Intravenous Doses of UCB0107 in Healthy Male SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Male Volunteers · study director
- Ph3NCT03412747 · A Study to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Plaque Psoriasis · study director
- Ph3NCT03410992 · A Study With a Initial Treatment Period Followed by a Randomized-withdrawal Period to Evaluate the Efficacy and Safety of Bimekizumab in Adult Subjects With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis, Psoriatic Arthritis · study director
- Ph2NCT03405714 · A Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Intravenous Brivaracetam in Subjects >= 1 Month to < 16 Years of Age With EpilepsyUCB Biopharma S.P.R.L. · completed · Epilepsy · study director
- Ph2NCT03373383 · Study to Test the Efficacy and Safety of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adults With Drug-resistant EpilepsyUCB Biopharma S.P.R.L. · completed · Drug-resistant Epilepsy, Focal-Onset Seizures · study director
- Ph2NCT03370120 · Study to Test the Safety and Efficacy of Padsevonil as Adjunctive Treatment of Focal-onset Seizures in Adult Subjects With Drug-resistant EpilepsyUCB Biopharma SRL · terminated · Drug-Resistant Epilepsy, Focal-Onset Seizures · study director
- Ph3NCT03370133 · A Study to Evaluate the Efficacy and Safety of Bimekizumab Compared to Placebo and an Active Comparator in Adult Subjects With Moderate to Severe Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis, Moderate to Severe Chronic Plaque Psoriasis, Psoriatic Arthritis · study director
- Ph3NCT03357471 · Study to Test the Safe and Effective Use of an e-Device for the Self-injection of Certolizumab Pegol Solution by Subjects With Moderate to Severe Active Rheumatoid Arthritis, Active Ankylosing Spondylitis, Active Psoriatic Arthritis, or Moderately to Severely Active Crohn's DiseaseUCB Biopharma S.P.R.L. · completed · Moderate and Severe Active Rheumatoid Arthritis, Active Psoriatic Arthritis, Active Ankylosing Spondylitis · study director
- Ph3NCT03355209 · A Study to Investigate the Efficacy and Safety of ZX008 (Fenfluramine Hydrochloride) as an Adjunctive Therapy in Children and Adults With Lennox-Gastaut SyndromeZogenix International Limited, Inc., a subsidiary of Zogenix, Inc. · completed · Lennox Gastaut Syndrome · study director
- Ph2NCT03355573 · A Study to Evaluate the Long Term Safety and Efficacy of Bimekizumab in Subjects With Ankylosing SpondylitisUCB Biopharma SRL · completed · Ankylosing Spondylitis · study director
- Ph2NCT03347110 · A Study to Evaluate the Long-Term Safety and Efficacy of Bimekizumab in Subjects With Psoriatic ArthritisUCB Biopharma SRL · completed · Psoriatic Arthritis · study director
- Ph3NCT03340064 · A Study of Levetiracetam as Monotherapy or Adjunctive Treatment of Partial Seizures in Pediatric Epileptic Subjects Ranging From 1 Month to Less Than 4 Years of AgeUCB Japan Co. Ltd. · completed · Partial Seizures · study director
- Ph3NCT03325439 · A Study to Test the Pharmacokinetics, Efficacy, and Safety of Brivaracetam in Newborns With Repeated Electroencephalographic SeizuresUCB Biopharma SRL · terminated · Electroencephalographic Neonatal Seizures · study director
- Ph2NCT03315130 · Safety and Efficacy Study of RA101495 in Subjects With Generalized Myasthenia GravisRa Pharmaceuticals · completed · Generalized Myasthenia Gravis · study director
- Ph3NCT03299842 · A Study to Assess the Usability of the Embrace Seizure Detection Watch in Children and Young Adults With Dravet SyndromeZogenix International Limited, Inc., a subsidiary of Zogenix, Inc. · terminated · Dravet Syndrome · study director
- Ph3NCT03250377 · A Study to Test the Safety/ Efficacy of Brivaracetam (BRV) Used as Adjunctive Treatment in Subjects >=16 Years of Age With Partial Seizures With or Without Secondary GeneralizationUCB Biopharma SRL · completed · Partial Seizures With or Without Secondary Generalization, Epilepsy · study director
- Ph2NCT03248531 · A Study to Test the Efficacy, Safety and Pharmacokinetics of Bimekizumab in Subjects With Moderate to Severe Hidradenitis Suppurativa.UCB Biopharma SRL · completed · Hidradenitis Suppurativa · study director
- Ph2NCT03230292 · A Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Adult Patients With Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis · study director
- Ph2NCT03215277 · A Study to Test the Efficacy and Safety of Bimekizumab and Certolizumab Pegol in Patients With Active Ankylosing SpondylitisUCB Biopharma SRL · completed · Ankylosing Spondylitis · study director
- Ph1NCT03204474 · A Study to Investigate the Bioequivalence of Lacosamide 200mg Administered as Intravenous Solution and Oral Tablet in Healthy Chinese Male SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Male Chinese Volunteers · study director
- Ph1NCT03168984 · A Study to Investigate the Safety, Tolerability, and Pharmacokinetics of UCB0942 in Healthy Japanese and Caucasian SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Japanese and Caucasian Subjects · study director
- Ph4NCT03103919 · Study to Evaluate the Impact of Using Wearable Devices in Addition to Standard Clinical Practice on Parkinson´s Subject Symptoms ManagementUCB Biopharma S.P.R.L. · completed · Parkinson´s Disease · study director
- Ph1NCT03086382 · A Study to Investigate the Bioequivalence of Lacosamide Tablet (200mg) and Syrup (10mg/ml) in Healthy Chinese Male SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Male Volunteers · study director
- Ph3NCT03083665 · A Study to Evaluate the Efficacy and Safety of Brivaracetam in Study Participants (>=16 to 80 Years of Age) With EpilepsyUCB Biopharma SRL · completed · Partial Seizures With or Without Secondary Generalization, Epilepsy · study director
- Ph2NCT03052751 · Study to Test the Safety, Tolerability and Efficacy of UCB7665 in Subjects With Moderate to Severe Myasthenia GravisUCB Biopharma S.P.R.L. · completed · Myasthenia Gravis · study director
- Ph2/Ph3NCT03051217 · A Study to Test the Efficacy and Safety of Certolizumab Pegol in Japanese Subjects With Moderate to Severe Chronic PsoriasisUCB Biopharma S.P.R.L. · completed · Moderate to Severe Psoriasis, Generalized Pustular Psoriasis and Erythrodermic Psoriasis · study director
- Ph2NCT03025542 · A Study to Evaluate the Pharmacokinetics (PK), Pharmacodynamics (PD), and Safety of Bimekizumab in Patients With Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis · study director
- Ph4NCT03020992 · A Study to Assess the Effects of Certolizumab Pegol on the Reduction of Anterior Uveitis (AU) Flares in Axial Spondyloarthritis Subjects With a Documented History of AUUCB Biopharma SRL · completed · Axial Spondyloarthritis (axSpA), Anterior Uveitis (AU) · study director
- Ph2NCT03021018 · A Study to Assess the Efficacy and Safety of Brivaracetam as Treatment for Increased Seizure Activity in an Epilepsy Monitoring Unit SettingUCB Biopharma S.P.R.L. · completed · Epilepsy · study director
- Ph2NCT03010527 · A Study to Evaluate the Long-term Safety, Tolerability and Efficacy of Bimekizumab in Patients With Chronic Plaque PsoriasisUCB Biopharma SRL · completed · Chronic Plaque Psoriasis · study director
- Ph1NCT02972125 · A Study to Demonstrate the Bioequivalence of Lacosamide Tablets and Dry Syrup in Healthy Male Japanese SubjectsUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- Ph2NCT02969525 · A Study to Evaluate the Dose Response Based on the Efficacy, Safety and Tolerability of Bimekizumab in Subjects With Active Psoriatic Arthritis Which is a Type of Inflammatory ArthritisUCB Biopharma S.P.R.L. · completed · Psoriatic Arthritis · study director
- Ph2NCT02963506 · A Study to Evaluate the Efficacy and Safety of Different Doses of Bimekizumab in Subjects With Active Ankylosing SpondylitisUCB Biopharma S.P.R.L. · completed · Ankylosing Spondylitis · study director
- Ph2NCT02905006 · Study to Evaluate Safety and Efficacy of Different Doses of Bimekizumab in Patients With Chronic Plaque PsoriasisUCB Biopharma S.P.R.L. · completed · Chronic Plaque Psoriasis · study director
- Ph1NCT02879877 · A First-In-Human Study With a Single Ascending Dose of UCB7858 in Healthy VolunteersUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- Ph1NCT02873767 · A First-In-Human Study With a Single Dose UCB4019 in Healthy VolunteersUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- Ph2NCT02829827 · A Phase 2 Study of Radiprodil in Subjects With Drug-resistant Infantile Spasms (IS)UCB Biopharma S.P.R.L. · terminated · Infantile Spasms (IS) · study director
- Ph3NCT02823145 · An Open-Label Extension Trial to Assess the Long-Term Safety of ZX008 (Fenfluramine Hydrochloride HCl) Oral Solution in Children and Young Adults With Dravet SyndromeZogenix International Limited, Inc., a subsidiary of Zogenix, Inc. · completed · Dravet Syndrome · study director
- Ph1NCT02806219 · Open-label, Bioequivalence Study of Certolizumab Pegol 200 mg Solution Injected Either by a Prefilled Syringe (Reference) or by an E-Device (Test) in Healthy SubjectsUCB BIOSCIENCES, Inc. · completed · Healthy · study director
- Ph2NCT02804763 · A Phase 2 Efficacy and Safety Study of Dapirolizumab Pegol (DZP) in Systemic Lupus ErythematosusUCB Biopharma S.P.R.L. · completed · Systemic Lupus Erythematosus (SLE) · study director
- N/ANCT02775656 · UCB Cimzia Pregnancy Follow-up StudyUCB BIOSCIENCES, Inc. · terminated · Rheumatoid Arthritis (RA), Crohn's Disease (CD), Psoriatic Arthritis (PsA) · study director
- Ph2NCT02718716 · Study to Evaluate Safety, Tolerability and Efficacy of UCB7665 in Subjects With Primary Immune ThrombocytopeniaUCB Biopharma SRL · completed · Thrombocytopenia · study director
- Ph2/Ph3NCT02710890 · Study to Investigate Safety and Tolerability of Intravenous Lacosamide in Children.UCB BIOSCIENCES, Inc. · completed · Epilepsy · study director
- N/ANCT02687711 · Study to Look at How Effective Briviact is as add-on Treatment for Patients With Epilepsy With Partial Onset SeizuresUCB Biopharma S.P.R.L. · completed · Epilepsy With POS With or Without Secondary Generalization · study director
- Ph3NCT02682927 · A Trial of Two Fixed Doses of ZX008 (Fenfluramine HCl) in Children and Young Adults With Dravet SyndromeZogenix International Limited, Inc., a subsidiary of Zogenix, Inc. · completed · Dravet Syndrome, Seizure Disorder · study director
- Ph1NCT02647697 · Study to Evaluate Properties of Radiprodil Given in Oral Solution to Healthy VolunteersUCB Biopharma S.P.R.L. · completed · Healthy Volunteers · study director
- Ph2NCT02625090 · An Open-label Extension Study of UCB0942 in Adult Patients With Highly Drug-resistant Focal EpilepsyUCB Biopharma SRL · terminated · Highly Drug-resistant Focal Epilepsy · study director
- Ph2NCT02610543 · UCB Proof of Concept Study in Patients With Primary Sjögren's SyndromeUCB Celltech · terminated · Primary Sjögren's Syndrome · study director
- Ph1NCT02602860 · A Brain Imaging Study With Positron Emission Tomography and the Radiotracer [11C]UCB-J to Estimate How Fast Brivaracetam and Levetiracetam Enter the Brain in Healthy VolunteersUCB Pharma · completed · Healthy Volunteers · study director
- Ph3NCT02582866 · A Clinical Study to Investigate the Long-term Use of Lacosamide as Monotherapy in Subjects Who Completed Study SP0994UCB Biopharma S.P.R.L. · completed · Epilepsy · study director
- Ph3NCT02552212 · Multicenter Study Evaluating Certolizumab Pegol Compared to Placebo in Subjects With axSpA Without X-ray Evidence of ASUCB BIOSCIENCES GmbH · completed · Axial Spondyloarthritis, Nonradiographic Axial Spondyloarthritis, Nr-axSpA · study director
- Ph3NCT02505542 · Study to Evaluate Maintenance of Sustained Remission of axSpA With CZP Compared to PlaceboUCB BIOSCIENCES GmbH · completed · Axial Spondyloarthrithis, Ankylosing Spondylitis · study director
- Ph2NCT02495844 · A Study of UCB0942 in Adult Patients With Highly Drug-resistant Focal EpilepsyUCB Biopharma S.P.R.L. · completed · Highly Drug-resistant Focal Epilepsy · study director
- Ph3NCT02477839 · Efficacy and Safety of Lacosamide as Adjunctive Therapy in Subjects ≥1 Month to <4 Years With Partial-onset SeizuresUCB BIOSCIENCES, Inc. · completed · Epilepsy With Partial-onset Seizures · study director
- Ph2NCT02430909 · Multiple Dose Study of UCB4940 as add-on to Certolizumab Pegol in Subjects With Rheumatoid ArthritisUCB Celltech · completed · Rheumatoid Arthritis · study director
- Ph3NCT02408549 · Safety and Efficacy of Lacosamide as Additional Therapy in Patients Suffering From Epileptic Tonic-Clonic SeizuresUCB BIOSCIENCES, Inc. · completed · Epilepsy · study director
- Ph3NCT02408523 · A Study to Assess the Safety and Efficacy of Lacosamide Versus Placebo (a Pill Without Active Medication) in Patients With Idiopathic Generalised Epilepsy Who Are Already Taking Anti-epileptic MedicationsUCB BIOSCIENCES, Inc. · completed · Epilepsy · study director
- N/ANCT02354105 · A Study to Assess the Effectiveness of Certolizumab Pegol in Patients With Axial Spondyloarthritis in Daily LifeUCB Biopharma S.P.R.L. · completed · Axial Spondyloarthritis · study director
- Ph3NCT02346240 · Efficacy and Safety Study of Certolizumab Pegol (CZP) Versus Active Comparator and Placebo in Subjects With Plaque Psoriasis (PSO)UCB Biopharma S.P.R.L. · completed · Psoriasis, Plaque Psoriasis · study director
- Ph3NCT02326272 · A Study to Evaluate the Efficacy and Safety of Two Dose Levels of Certolizumab Pegol (CZP) in Subjects With Plaque Psoriasis (PSO)UCB Biopharma S.P.R.L. · completed · Psoriasis, Plaque Psoriasis · study director
- Ph3NCT02326298 · An Efficacy and Safety Study of Two Dose Levels of Certolizumab Pegol (CZP) in Subjects With Plaque Psoriasis (PSO)UCB Biopharma S.P.R.L. · completed · Psoriasis, Plaque Psoriasis · study director
- Ph3NCT02319642 · An Open-label Extension Study of Certolizumab Pegol in Chinese Patients With Rheumatoid Arthritis Who Enrolled in RA0044UCB Pharma SA · completed · Rheumatoid Arthritis · study director
- Ph1NCT02303509 · Study to Assess Safety, Tolerability, Pharmacokinetic & Pharmacodynamic Effect of UCB5857 in Healthy & Psoriatic SubjectUCB Pharma · completed · Psoriasis · study director
- N/ANCT02276053 · Study of Lacosamide as an Adjunctive Drug Treatment for Epilepsy in Patients With Brain TumorsUCB BIOSCIENCES GmbH · completed · Brain Tumor Related Epilepsy (BTRE) · study director
- Ph1NCT02154425 · A Multicenter, Postmarketing Study Evaluating the Concentration of Cimzia® in Mature Breast Milk of Lactating MothersUCB BIOSCIENCES, Inc. · completed · Axial Spondyloarthritis (AxSpA), Non-radiographic Evidence-AxSpA, Ankylosing Spondylitis · study director
- Ph3NCT02151851 · A Study of Certolizumab Pegol as Additional Therapy in Chinese Patients With Active Rheumatoid ArthritisUCB Pharma SA, Belgium · completed · Rheumatoid Arthritis · study director
- Ph3NCT02124564 · A Trial to Evaluate the Long Term Safety and Tolerability of Lacosamide Taken as Monotherapy in Adults With Partial-onset SeizuresUCB Japan Co. Ltd. · completed · Epilepsy, Partial-onset Seizures · study director
Grants
NIH projects from RePORTER, fetched 2026-11-11 23:55 UTC. A project is listed only when its grant number is on one of the trials above, or when the awardee institution matches an affiliation the registry gives for this name. Coverage is US federal funding only; UK and EU funders are not searched yet.
No NIH project could be tied to this name by a shared trial or a matching institution.
Most cited trial papers
PubMed returned no clinical-trial papers for this author name.