13. 多発性硬化症/視神経脊髄炎 Multiple sclerosis/Neuromyelitis optica Clinical trials / Disease details
臨床試験数 : 3,342 / 薬物数 : 2,355 - (DrugBank : 406) / 標的遺伝子数 : 269 - 標的パスウェイ数 : 241
Showing 1 to 10 of 160 diseases
No. | TrialID | Date_ enrollment | Date_ registration | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
1 | NCT05265728 (ClinicalTrials.gov) | March 25, 2022 | 23/2/2022 | A Study to Evaluate Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of Natalizumab (BG00002) Administered Subcutaneously to Japanese Participants With Relapsing-Remitting Multiple Sclerosis A Study to Evaluate Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of Na ... | A Single-Arm, Open-Label, Phase 3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of Natalizumab (BG00002) Administered to Japanese Participants With Relapsing-Remitting Multiple Sclerosis Via a Subcutaneous Route of Administration A Single-Arm, Open-Label, Phase 3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Phar ... | Multiple Sclerosis, Relapsing-Remitting | Drug: Natalizumab | Biogen | NULL | Not yet recruiting | 18 Years | 65 Years | All | 20 | Phase 3 | NULL |
2 | JPRN-jRCT2051210146 | 24/02/2022 | 26/12/2021 | Phase 3 Study to Evaluate Efficacy, Safety, PK, and PD of SC Natalizumab in Japanese Participants With RRMS Phase 3 Study to Evaluate Efficacy, Safety, PK, and PD of SC Natalizumabin Japanese Participants Wit ... | A Single-Arm, Open-Label, Phase 3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Pharmacodynamics of Multiple Doses of Natalizumab (BG00002) Administered to Japanese Participants With Relapsing-Remitting Multiple Sclerosis via a Subcutaneous Route of Administration A Single-Arm, Open-Label, Phase 3 Study to Evaluate the Efficacy, Safety, Pharmacokinetics, and Phar ... | Relapsing-Remitting Multiple Sclerosis | Participants will receive natalizumab 300 mg SC Q4W for 48 weeks. | Amir Hadi Maghzi | NULL | Pending | >= 18age old | <= 65age old | Both | 20 | Phase 3 | Japan |
3 | NCT05177718 (ClinicalTrials.gov) | January 1, 2022 | 13/12/2021 | Natalizumab and Chronic Inflammation | Assessing the Effect of Natalizumab of Magnetic Resonance Imaging Measures of Blood Brain Barrier Permeability and Myelin Integrity Assessing the Effect of Natalizumabof Magnetic Resonance Imaging Measures of Blood Brain Barrier Per ... | Multiple Sclerosis | Drug: Natalizumab 300 MG in 15 ML Injection | Vanderbilt University Medical Center | Biogen | Recruiting | 18 Years | 65 Years | All | 36 | Phase 4 | United States |
4 | NCT04777539 (ClinicalTrials.gov) | June 17, 2021 | 23/2/2021 | Comparing the Safety and Benefit of Natalizumab (Tysabri®) At-home Infusion vs At-hospital Infusion in Multiple Sclerosis Comparing the Safety and Benefit of Natalizumab(Tysabri®) At-home Infusion vs At-hospital Infusion i ... | Assessing the Safety and Benefit of Home-hospitalization Program in the Management of Natalizumab (Tysabri®) Medication in Multiple Sclerosis Assessing the Safety and Benefit of Home-hospitalization Program in the Management of Natalizumab(Ty ... | Multiple Sclerosis (MS) | Other: At-home natalizumab treated MS patient | Nantes University Hospital | Rennes University Hospital | Recruiting | 18 Years | N/A | All | 315 | France | |
5 | NCT04964700 (ClinicalTrials.gov) | May 6, 2021 | 27/5/2021 | Analysis of MS Patients Who Have Had Greater Than 60 Infusions of Natalizumab | Analysis of Multiple Sclerosis Patients Who Have Had Greater Than 60 Infusions of Natalizumab: Safety and Efficacy Analysis of Multiple Sclerosis Patients Who Have Had Greater Than 60 Infusions of Natalizumab: Safet ... | Multiple Sclerosis | Drug: Natalizumab | Multiple Sclerosis Center of Northeastern New York | NULL | Active, not recruiting | 18 Years | N/A | All | 60 | United States | |
6 | NCT04580381 (ClinicalTrials.gov) | September 1, 2020 | 2/10/2020 | Real World Effectiveness of Natalizumab Extended Interval Dosing in a French Cohort | Real World Effectiveness of Natalizumab Extended Interval Dosing in Relapsing-Remitting Multiple Sclerosis in a French Cohort Real World Effectiveness of NatalizumabExtended Interval Dosing in Relapsing-Remitting Multiple Scle ... | Multiple Sclerosis, Relapsing-Remitting | Drug: Natalizumab Injection [Tysabri] | University Hospital, Caen | Biogen | Completed | 18 Years | N/A | All | 500 | France | |
7 | EUCTR2019-003127-38-NL (EUCTR) | 09/04/2020 | 09/04/2020 | Research on the effect of add-on high dosage simvastatin treatment on progression in MS patients treated with ocrelizumab and natalizumab. Research on the effect of add-on high dosage simvastatin treatment on progression in MS patients tre ... | Efficacy of add-on high dose simvastatin on markers for disease progression in MS patients treated with ocrelizumab and natalizumab (SIMSON), a phase II clinical trial. - SIMSON trial Efficacy of add-on high dose simvastatin on markers for disease progression in MS patients treated w ... | Multiple sclerosis;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] | Product Name: Simvastatin INN or Proposed INN: SIMVASTATIN Other descriptive name: Simvastatine | VUmc Neurology Department | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 100 | Phase 2 | Netherlands | ||
8 | NCT04178005 (ClinicalTrials.gov) | February 19, 2020 | 21/11/2019 | Cladribine Tablets After Treatment With Natalizumab (CLADRINA) | Cladribine Tablets After Treatment With Natalizumab (CLADRINA) | Multiple Sclerosis | Drug: Cladribine | University of Texas Southwestern Medical Center | EMD Serono | Recruiting | 18 Years | 60 Years | All | 40 | Phase 4 | United States |
9 | NCT04225312 (ClinicalTrials.gov) | February 3, 2020 | 3/1/2020 | Personalized Extended Interval Dosing of Natalizumab in Relapsing Remitting Multiple Sclerosis | Personalized Extended Interval Dosing of Natalizumab in Relapsing Remitting Multiple Sclerosis | Relapsing Remitting Multiple Sclerosis | Drug: Personalized extended interval dosing of natalizumab;Drug: Standard interval dosing | VU University Medical Center | Stichting MS Research;Innovatiefonds Zorgverzekeraard | Recruiting | 18 Years | N/A | All | 300 | Phase 4 | Netherlands |
10 | EUCTR2019-002566-13-NL (EUCTR) | 19/12/2019 | 29/10/2019 | Personalizing the treatment with natalizumab in patients with multiple sclerosis | Personalized extended interval dosing of natalizumab in relapsing remitting multiple sclerosis - NEXT-MS Personalized extended interval dosing of natalizumabin relapsing remitting multiple sclerosis - NEXT ... | Relapsing remitting multiple sclerosis MedDRA version: 20.1;Level: LLT;Classification code 10070425;Term: Multiple sclerosis exacerbation;System Organ Class: 100000004852 ;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] Relapsing remitting multiple sclerosis MedDRA version: 20.1;Level: LLT;Classification code 10070425; ... | Trade Name: Tysabri Product Name: natalizumab | Amsterdam University Medical Center | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 300 | Human pharmacology (Phase 1): no Therapeutic exploratory (Phase 2): no Therapeutic confirmatory - (Phase 3): no Therapeutic use (Phase 4): yes Human pharmacology (Phase 1): no Therapeutic exploratory (Phase 2): no Therapeutic confirmatory - (P ... | Netherlands |