11. Myasthenia gravis Clinical trials / Disease details
Clinical trials : 332 / Drugs : 234 - (DrugBank : 81) / Drug target genes : 45 - Drug target pathways : 127
Showing 1 to 10 of 332 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 |
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1 | NCT05681715 (ClinicalTrials.gov) | March 9, 2023 | 4/1/2023 | A Phase 3, Open-label, Crossover Study to Evaluate Self-administration of Rozanolixizumab by Study Participants With Generalized Myasthenia Gravis (gMG) A Phase 3, Open-label, Crossover Study to Evaluate Self-administration of Rozanolixizumab by Study P ... | An Open-label, Crossover Study to Evaluate Rozanolixizumab Self-administration by Study Participants With Generalized Myasthenia Gravis An Open-label, Crossover Study to Evaluate Rozanolixizumab Self-administration by Study Participants ... | Generalized Myasthenia Gravis | Drug: Rozanolixizumab | UCB Biopharma SRL | NULL | Not yet recruiting | 18 Years | N/A | All | 30 | Phase 3 | NULL |
2 | NCT05644561 (ClinicalTrials.gov) | January 2, 2023 | 1/12/2022 | Evaluation of Pharmacokinetics, Pharmacodynamics, Efficacy, Safety, and Immunogenicity of Ravulizumab Administered Intravenously in Pediatric Participants With Generalized Myasthenia Gravis (gMG) Evaluation of Pharmacokinetics, Pharmacodynamics, Efficacy, Safety, and Immunogenicity of Ravulizuma ... | A Phase 3, Open-label, Single-arm, Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Efficacy, Safety, and Immunogenicity of Ravulizumab Administered Intravenously in Pediatric Participants (6 to < 18 Years of Age) With Generalized Myasthenia Gravis (gMG) A Phase 3, Open-label, Single-arm, Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynam ... | Generalized Myasthenia Gravis;gMG | Drug: Ravulizumab | Alexion Pharmaceuticals | NULL | Not yet recruiting | 6 Years | 18 Years | All | 12 | Phase 3 | NULL |
3 | NCT05451212 (ClinicalTrials.gov) | November 23, 2022 | 30/6/2022 | Open-label Study to Evaluate the Safety of Various Dosing Regimens of MuSK-CAART for MuSK Myasthenia Gravis Open-label Study to Evaluate the Safety of Various Dosing Regimens of MuSK-CAART for MuSK Myasthenia ... | A Phase 1, Open-label, Safety and Dose-finding Study of Autologous Muscle-specific Tyrosine Kinase Chimeric Autoantibody Receptor T Cells (MuSK-CAART) in Subjects With Anti-MuSK-antibody-positive Myasthenia Gravis A Phase 1, Open-label, Safety and Dose-finding Study of Autologous Muscle-specific Tyrosine Kinase C ... | MuSK Myasthenia Gravis | Biological: MuSK-CAART | Cabaletta Bio | NULL | Recruiting | 18 Years | N/A | All | 24 | Phase 1 | United States |
4 | NCT05514873 (ClinicalTrials.gov) | October 31, 2022 | 22/8/2022 | 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 Inhibitors An Open-label Study to Evaluate the Safety, Tolerability, and Efficacy of Subcutaneous Zilucoplan in ... | A Phase 3b, Multicenter, Open-Label, Single-Arm Study to Evaluate the Safety, Tolerability, and Efficacy of Zilucoplan in Participants With Generalized Myasthenia Gravis Switching From Intravenous Complement Component 5 Inhibitors to Subcutaneous Zilucoplan A Phase 3b, Multicenter, Open-Label, Single-Arm Study to Evaluate the Safety, Tolerability, and Effi ... | Generalized Myasthenia Gravis | Drug: zilucoplan (RA101495) | UCB Biopharma SRL | NULL | Recruiting | 18 Years | 85 Years | All | 20 | Phase 3 | United States |
5 | JPRN-jRCT2031220102 | 28/10/2022 | 31/05/2022 | A Study of Nipocalimab in Children Aged 2 to less than 18 Years with Generalized Myasthenia Gravis | An Open-Label Uncontrolled Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Activity of Nipocalimab in Children Aged 2 to less than 18 years with Generalized Myasthenia Gravis An Open-Label Uncontrolled Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Saf ... | Myasthenia Gravis | Nipocalimab will be administered as an IV infusion. Participants aged 2 to less than [<] 18 years of age will receive nipocalimab once every two weeks for 24 weeks. After Week 24, all participants will have the option to enroll in long term extension (LTE). Nipocalimabwill be administered as an IV infusion. Participants aged 2 to less than [<] 18 years of a ... | Nakano Masayoshi | NULL | Pending | >= 2age old | <= 17age old | Both | 12 | Phase 2 | Canada;Netherlands;nitedStates of America;Japan |
6 | EUCTR2021-002460-46-AT (EUCTR) | 16/09/2022 | 23/05/2022 | Evaluating Long-term Safety of Efgartigimod Administered Intravenously in Children With Generalized Myasthenia Gravis Evaluating Long-term Safety of Efgartigimod Administered Intravenously in Children With Generalized ... | A Long-term, Single-Arm, Open-label, Multicenter, Follow-on Trial of ARGX113-2006 to Evaluate Safety of Efgartigimod Administered Intravenously inChildren With Generalized Myasthenia Gravis - ADAPT JR.+ A Long-term, Single-Arm, Open-label, Multicenter, Follow-on Trial of ARGX113-2006 to Evaluate Safety ... | Generalized Myasthenia Gravis MedDRA version: 21.1;Level: PT;Classification code 10028417;Term: Myasthenia gravis;System Organ Class: 10029205 - Nervous system disorders;Therapeutic area: Diseases [C] - Immune System Diseases [C20] Generalized Myasthenia Gravis MedDRA version: 21.1;Level: PT;Classification code 10028417;Term: Myas ... | Product Name: efgartigimod Product Code: argx-113 INN or Proposed INN: EFGARTIGIMOD ALFA | argenx BV | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 12 | Phase 2;Phase 3 | France;United States;Canada;Belgium;Spain;Poland;Austria;Georgia;Germany;Netherlands;United Kingdom;Italy France;United States;Canada;Belgium;Spain;Poland;Austria;Georgia;Germany;Netherlands;United Kingdom; ... | ||
7 | NCT05374590 (ClinicalTrials.gov) | August 18, 2022 | 1/4/2022 | Evaluating Long-term Safety of Efgartigimod Administered Intravenously in Children With Generalized Myasthenia Gravis Evaluating Long-term Safety of Efgartigimod Administered Intravenously in Children With Generalized ... | A Long-term, Single-Arm, Open-label, Multicenter, Follow-on Trial of ARGX-113-2006 to Evaluate Safety of Efgartigimod Administered Intravenously in Children With Generalized Myasthenia Gravis A Long-term, Single-Arm, Open-label, Multicenter, Follow-on Trial of ARGX-113-2006 to Evaluate Safet ... | Generalized Myasthenia Gravis | Biological: Efgartigimod IV | argenx | NULL | Recruiting | 2 Years | 18 Years | All | 12 | Phase 2/Phase 3 | Netherlands;Poland |
8 | NCT05390840 (ClinicalTrials.gov) | August 2022 | 20/5/2022 | A Study to Investigate the Effect on Central Macular Thickness of Treatment With MG-O-1002 Eye Drops in Participants Aged Over 45 With Neovascular Age-related Macular Degeneration (nAMD) A Study to Investigate the Effect on Central Macular Thickness of Treatment With MG-O-1002 Eye Drops ... | A Phase II Trial to Evaluate the Efficacy and Safety of Topical Ocular MG-O-1002 in Patients With Neovascular Age-Related Macular Degeneration (nAMD) A Phase II Trial to Evaluate the Efficacy and Safety of Topical Ocular MG-O-1002 in Patients With Ne ... | Age-Related Macular Degeneration | Drug: MG-O-1002;Other: Placebo | Theratocular Biotek Co. | NULL | Not yet recruiting | 45 Years | N/A | All | 36 | Phase 2 | NULL |
9 | NCT05067348 (ClinicalTrials.gov) | July 21, 2022 | 23/9/2021 | Efficacy and Safety of Tocilizumab in the Treatment of Generalized Myasthenia Gravis | A Multi-center, Randomized, Double-blind, Placebo-controlled Clinical Trial of the Efficacy and Safety of Tocilizumab in the Treatment of Generalized Myasthenia Gravis A Multi-center, Randomized, Double-blind, Placebo-controlled Clinical Trial of the Efficacy and Safe ... | Myasthenia Gravis, Generalized | Drug: Tocilizumab Injectable Product | Tang-Du Hospital | NULL | Recruiting | 18 Years | 80 Years | All | 64 | Phase 2 | China |
10 | NCT05265273 (ClinicalTrials.gov) | July 20, 2022 | 22/2/2022 | A Study of Nipocalimab in Children Aged 2 to Less Than 18 Years With Generalized Myasthenia Gravis | An Open-Label Uncontrolled Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Safety and Activity of Nipocalimab in Children Aged 2 to Less Than 18 Years With Generalized Myasthenia Gravis An Open-Label Uncontrolled Multicenter Study to Evaluate the Pharmacokinetics, Pharmacodynamics, Saf ... | Myasthenia Gravis | Drug: Nipocalimab | Janssen Research & Development, LLC | NULL | Recruiting | 2 Years | 17 Years | All | 12 | Phase 2/Phase 3 | United States;Canada;Japan;Netherlands;Poland |