- Trials with a EudraCT protocol (79)
- Paediatric studies in scope of Art45 of the Paediatric Regulation (0)
79 result(s) found for: Autoimmune Diseases of the Nervous System.
Displaying page 2 of 4.
EudraCT Number: 2022-003870-21 | Sponsor Protocol Number: MG0020 | Start Date*: 2023-07-25 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: An open-label, crossover study to evaluate rozanolixizumab self-administration by study participants with generalized Myasthenia Gravis | |||||||||||||
Medical condition: Generalized Myasthenia Gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) ES (Ongoing) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001579-30 | Sponsor Protocol Number: TV5600-CNS-20006 | Start Date*: 2014-11-27 | |||||||||||
Sponsor Name:Teva Pharmaceutical Industries Ltd. | |||||||||||||
Full Title: A Multinational, Multicenter, Randomized, Double-Blind, Parallel-Group, Placebo-Controlled Study to Evaluate the Efficacy, Safety, and Tolerability of Once Daily Oral Administration of Laquinimod (... | |||||||||||||
Medical condition: Primary Progressive Multiple Sclerosis | |||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||
Trial protocol: GB (Completed) IT (Completed) ES (Completed) DE (Completed) NL (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2020-003230-20 | Sponsor Protocol Number: MG0007 | Start Date*: 2020-11-30 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: An Open-Label Extension Study to Evaluate Rozanolixizumab in Study Participants With Generalized Myasthenia Gravis | |||||||||||||
Medical condition: Generalized myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) DE (Completed) CZ (Completed) FR (Completed) PL (Completed) HU (Completed) DK (Completed) BE (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2016-002698-36 | Sponsor Protocol Number: MG0002 | Start Date*: 2017-02-09 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Multicenter, Randomized, Investigator- and Subject-Blind, Placebo-Controlled, Treatment Sequence Study Evaluating the Safety, Tolerability, and Efficacy of UCB7665 in Subjects with Moderate to Se... | |||||||||||||
Medical condition: Moderate to severe myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) BE (Completed) ES (Completed) CZ (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2018-000780-91 | Sponsor Protocol Number: ML40359 | Start Date*: 2018-04-26 | |||||||||||||||||||||
Sponsor Name:ROCHE | |||||||||||||||||||||||
Full Title: AN OPEN-LABEL, SINGLE-ARM PHASE IV STUDY TO ASSESS OCRELIZUMAB EFFICACY, SAFETY AND IMPACT ON PATIENT REPORTED OUTCOMES (PROS) IN PATIENTS WITH ACTIVE RELAPSING MULTIPLE SCLEROSIS (PRO-MSACTIVE) | |||||||||||||||||||||||
Medical condition: ACTIVE RELAPSING MULTIPLE SCLEROSIS (Active RMS) | |||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: FR (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2017-004886-29 | Sponsor Protocol Number: MN39158 | Start Date*: 2018-05-22 | ||||||||||||||||||||||||||
Sponsor Name:Roche Farma SA (Soc unipersonal) que realiza el ensayo en España y que actúa como representante F.Hoffmann-La Roche Ltd | ||||||||||||||||||||||||||||
Full Title: A SINGLE ARM, OPEN LABEL MULTICENTRE EXTENSION STUDY TO EVALUATE THE EFFECTIVENESS AND SAFETY OF OCRELIZUMAB IN PATIENTS WITH MULTIPLE SCLEROSIS PREVIOUSLY ENROLLED IN A F. HOFFMANN-LA ROCHE SPONSO... | ||||||||||||||||||||||||||||
Medical condition: Multiple sclerosis (MS) | ||||||||||||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||||||||||||
Trial protocol: ES (Prematurely Ended) EE (Completed) IE (Completed) CZ (Completed) FR (Trial now transitioned) DK (Trial now transitioned) SE (Trial now transitioned) FI (Completed) NL (Trial now transitioned) GB (GB - no longer in EU/EEA) BE (Trial now transitioned) SI (Trial now transitioned) PL (Trial now transitioned) PT (Trial now transitioned) SK (Trial now transitioned) BG (Trial now transitioned) HU (Trial now transitioned) IT (Trial now transitioned) HR (Trial now transitioned) | ||||||||||||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2018-002133-37 | Sponsor Protocol Number: ARGX-113-1705 | Start Date*: 2019-06-06 | |||||||||||||||||||||
Sponsor Name:argenx BVBA | |||||||||||||||||||||||
Full Title: A Long-Term, Single-Arm, Open-Label, Multicenter, Phase 3 Follow-on Trial of ARGX-113-1704 to Evaluate the Safety and Tolerability of ARGX-113 in Patients with Myasthenia Gravis having Generalized... | |||||||||||||||||||||||
Medical condition: Myasthenia Gravis | |||||||||||||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||||||||||||
Trial protocol: NL (Completed) CZ (Completed) DE (Completed) DK (Completed) BE (Completed) HU (Completed) IT (Completed) | |||||||||||||||||||||||
Trial results: View results |
EudraCT Number: 2015-000097-35 | Sponsor Protocol Number: CCFZ533X2204 | Start Date*: 2015-09-02 | |||||||||||
Sponsor Name:Novartis Pharma Services AG | |||||||||||||
Full Title: A multi-center, randomized, double-blind, placebo-controlled, parallel group study to preliminarily evaluate the safety, tolerability, pharmacokinetics and efficacy of CFZ533 in patients with moder... | |||||||||||||
Medical condition: Acquired myasthenia gravis (MG) is an autoimmune disease that leads to fluctuating muscle weakness and fatigue. In the most common cases, muscle weakness is caused by circulating antibodies that bi... | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Completed) DK (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000969-21 | Sponsor Protocol Number: MG0004 | Start Date*: 2019-12-04 | |||||||||||
Sponsor Name:UCB Biopharma SPRL | |||||||||||||
Full Title: A Randomized, Open-Label Extension Study to Investigate the Long-Term Safety, Tolerability, and Efficacy of Rozanolixizumab in Adult Patients With Generalized Myasthenia Gravis | |||||||||||||
Medical condition: Generalized myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: HU (Completed) GB (GB - no longer in EU/EEA) DK (Completed) BE (Completed) DE (Completed) ES (Restarted) CZ (Completed) PL (Completed) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2013-001422-25 | Sponsor Protocol Number: ITA-BGT-12-10389 | Start Date*: 2013-06-11 | |||||||||||
Sponsor Name:Biogen Idec Italia S.r.l. | |||||||||||||
Full Title: Single country study assessing cognition in Relapsing Remitting Multiple Sclerosis patients treated with BG00012 | |||||||||||||
Medical condition: Relapsing Remitting Multiple Sclerosis (RRMS) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000968-18 | Sponsor Protocol Number: MG0003 | Start Date*: 2019-09-06 | |||||||||||
Sponsor Name:UCB Biopharma SRL | |||||||||||||
Full Title: A Phase 3, Randomized, Double-Blind, Placebo-Controlled Study Evaluating Efficacy and Safety of Rozanolixizumab in Adult Patients With Generalized Myasthenia Gravis. | |||||||||||||
Medical condition: Generalized myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) GB (GB - no longer in EU/EEA) PL (Completed) DE (Completed) HU (Completed) CZ (Completed) BE (Completed) ES (Restarted) IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2019-000895-40 | Sponsor Protocol Number: BETA-MG-01 | Start Date*: 2019-03-28 | |||||||||||
Sponsor Name:Aarhus University Hospital | |||||||||||||
Full Title: Beta-agonist Efficacy and Tolerability as Adjuvant therapy in Myasthenia Gravis | |||||||||||||
Medical condition: Myasthenia Gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DK (Completed) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-001313-93 | Sponsor Protocol Number: MN39159 | Start Date*: 2018-05-03 | ||||||||||||||||
Sponsor Name:F. Hoffmann-La Roche Ltd | ||||||||||||||||||
Full Title: AN OPEN-LABEL, SINGLE-ARM 4-YEAR STUDY TO EVALUATE EFFECTIVENESS AND SAFETY OF OCRELIZUMAB TREATMENT IN PATIENTS WITH PROGRESSIVE MULTIPLE SCLEROSIS | ||||||||||||||||||
Medical condition: Progressive multiple sclerosis (PMS) | ||||||||||||||||||
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Population Age: Adults | Gender: Male, Female | |||||||||||||||||
Trial protocol: IE (Completed) DK (Trial now transitioned) ES (Ongoing) PL (Trial now transitioned) FR (Trial now transitioned) CZ (Trial now transitioned) HU (Completed) IT (Trial now transitioned) DE (Trial now transitioned) | ||||||||||||||||||
Trial results: (No results available) |
EudraCT Number: 2020-003146-36 | Sponsor Protocol Number: RIAlta-1 | Start Date*: 2023-11-15 |
Sponsor Name:Vall d'Hebron Research Institute (VHIR) | ||
Full Title: Safety of Rifampicin at High Dose for the Treatment of Adult Subjects with Complex Drug Susceptible Pulmonary and Extrapulmonary Tuberculosis | ||
Medical condition: Pulmonary and extrapulmonary tuberculosis | ||
Disease: | ||
Population Age: Adults, Elderly | Gender: Male, Female | |
Trial protocol: NL (Ongoing) ES (Ongoing) | ||
Trial results: (No results available) |
EudraCT Number: 2020-000949-14 | Sponsor Protocol Number: VIB0551.P3.S1 | Start Date*: 2020-11-16 | |||||||||||
Sponsor Name:Viela Bio, Inc. | |||||||||||||
Full Title: A RANDOMIZED, DOUBLE-BLIND, MULTICENTER, PLACEBO-CONTROLLED PHASE 3 STUDY WITH OPEN-LABEL PERIOD TO EVALUATE THE EFFICACY AND SAFETY OF INEBILIZUMAB IN ADULTS WITH MYASTHENIA GRAVIS | |||||||||||||
Medical condition: Myasthenia Gravis which is either due to acetylcholine receptor antibodies (AChR) or muscle specific kinase antibodies (MuSK). | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: FR (Trial now transitioned) DK (Prematurely Ended) DE (Trial now transitioned) IT (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2019-003107-35 | Sponsor Protocol Number: ARGX-113-1902 | Start Date*: 2020-07-15 | |||||||||||
Sponsor Name:argenx BVBA | |||||||||||||
Full Title: Open-label Extension of the ARGX-113-1802 Trial to Investigate the Long-term Safety, Tolerability, and Efficacy of Efgartigimod PH20 SC in Patients With Chronic Inflammatory Demyelinating Polyneuro... | |||||||||||||
Medical condition: Chronic Inflammatory Demyelinating Polyneuropathy | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: DE (Trial now transitioned) CZ (Completed) BE (Trial now transitioned) HU (Completed) PL (Trial now transitioned) GB (GB - no longer in EU/EEA) NL (Trial now transitioned) ES (Trial now transitioned) BG (Trial now transitioned) DK (Trial now transitioned) AT (Trial now transitioned) FR (Trial now transitioned) IT (Trial now transitioned) RO (Trial now transitioned) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-003008-30 | Sponsor Protocol Number: 16/0730 | Start Date*: 2020-07-01 | |||||||||||
Sponsor Name:University College London | |||||||||||||
Full Title: A double-blind, randomised, placebo-controlled single-site study of high dose simvastatin treatment for secondary progressive multiple sclerosis: impact on vascular perfusion and oxidative damage | |||||||||||||
Medical condition: Multiple Sclerosis (Secondary Progressive) | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: GB (GB - no longer in EU/EEA) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004018-25 | Sponsor Protocol Number: MSK-002 | Start Date*: 2018-02-22 | |||||||||||
Sponsor Name:CATALYST PHARMACEUTICALS INC. | |||||||||||||
Full Title: A Randomized, Placebo-Controlled, Parallel Group Study to Evaluate the Effect of Amifampridine Phosphate in Patients with MuSK Antibody Positive Myasthenia Gravis, and a Sample of AChR Antibody Pos... | |||||||||||||
Medical condition: MuSK antibody positive myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Completed) | |||||||||||||
Trial results: View results |
EudraCT Number: 2014-001355-23 | Sponsor Protocol Number: 40960 | Start Date*: 2014-08-29 | |||||||||||
Sponsor Name:Leiden University Medical Center | |||||||||||||
Full Title: Ephedrine as add-on therapy for patients with myasthenia gravis | |||||||||||||
Medical condition: myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: NL (Ongoing) | |||||||||||||
Trial results: (No results available) |
EudraCT Number: 2017-004777-14 | Sponsor Protocol Number: MSK-003 | Start Date*: 2018-06-05 | |||||||||||
Sponsor Name:CATALYST PHARMACEUTICALS INC. | |||||||||||||
Full Title: Long term safety study of amifampridine phosphate in patients with MuSK antibody positive and AChR antibody positive myasthenia gravis patients | |||||||||||||
Medical condition: MuSK antibody and AChR antibody positive myasthenia gravis | |||||||||||||
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Population Age: Adults, Elderly | Gender: Male, Female | ||||||||||||
Trial protocol: IT (Prematurely Ended) | |||||||||||||
Trial results: (No results available) |
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