17. 多系統萎縮症 Multiple system atrophy Clinical trials / Disease details
臨床試験数 : 119 / 薬物数 : 138 - (DrugBank : 44) / 標的遺伝子数 : 59 - 標的パスウェイ数 : 111
Showing 1 to 10 of 119 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 | NCT05634876 (ClinicalTrials.gov) | April 2023 | 23/11/2022 | UB-312 in Patients With Synucleinopathies | A Phase 1b Clinical Trial of UB-312 in Patients With Synucleinopathies | Multiple System Atrophy;Parkinson Disease | Biological: UB-312 Injection;Biological: Placebo Injection | NYU Langone Health | NULL | Not yet recruiting | 40 Years | 75 Years | All | 8 | Phase 1/Phase 2 | United States |
2 | NCT04680065 (ClinicalTrials.gov) | April 2023 | 15/12/2020 | GDNF Gene Therapy for Multiple System Atrophy | Randomized, Double-Blind, Placebo-controlled Safety Study of Glial Cell Line-Derived Neurotrophic Factor Gene Transfer (AAV2-GDNF) in Multiple System Atrophy Randomized, Double-Blind, Placebo-controlled Safety Study of Glial Cell Line-Derived Neurotrophic Fa ... | Multiple System Atrophy | Biological: AAV2-GDNF gene therapy;Procedure: Sham (Placebo) Surgery | Brain Neurotherapy Bio, Inc. | NULL | Recruiting | 35 Years | 75 Years | All | 9 | Phase 1 | United States |
3 | NCT05732415 (ClinicalTrials.gov) | March 1, 2023 | 8/2/2023 | Biomarker Study of ATH434 in Participants With MSA | An Open-Label Biomarker Study of ATH434 in Multiple System Atrophy | Multiple System Atrophy | Drug: ATH434 | Alterity Therapeutics | NULL | Not yet recruiting | 30 Years | 75 Years | All | 15 | Phase 2 | United States |
4 | NCT05696717 (ClinicalTrials.gov) | March 2023 | 13/1/2023 | Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participants With Multiple System Atrophy Phase 3 Efficacy and Durability of Ampreloxetine for the Treatment of Symptomatic nOH in Participant ... | A Phase 3, Multi-center, Randomized Withdrawal and Long Term Extension Study of Ampreloxetine for the Treatment of Symptomatic Neurogenic Orthostatic Hypotension in Participants With Multiple System Atrophy A Phase 3, Multi-center, Randomized Withdrawal and Long Term Extension Study of Ampreloxetine for th ... | Symptomatic Neurogenic Orthostatic Hypotension;MSA - Multiple System Atrophy | Drug: Ampreloxetine;Drug: Placebo | Theravance Biopharma | NULL | Not yet recruiting | 30 Years | N/A | All | 102 | Phase 3 | NULL |
5 | NCT05695378 (ClinicalTrials.gov) | February 27, 2023 | 22/12/2022 | Trial to Evaluate the Efficacy and Safety of KM-819 Treatment to Slow the Progression of Multiple System Atrophy (MSA) Trial to Evaluate the Efficacy and Safety of KM-819 Treatment to Slow the Progression of Multiple Sy ... | A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of KM-819 Treatment to Slow the Progression of Multiple System Atrophy A Phase 2, Randomized, Double-Blind, Placebo-Controlled Trial to Evaluate the Efficacy and Safety of ... | Multiple System Atrophy | Drug: KM-819;Drug: Placebo | Kainos Medicine Inc. | Parexel | Recruiting | 30 Years | 80 Years | All | 78 | Phase 2 | Korea, Republic of |
6 | NCT05486806 (ClinicalTrials.gov) | February 1, 2023 | 2/8/2022 | Longitudinal Tracking of Patients Diagnosed With Neurodegenerative Movement Disorders | Longitudinal Tracking of Patients Diagnosed With Neurodegenerative Movement Disorders | Neurodegenerative Diseases;sca3;MSA - Multiple System Atrophy;Ataxia;Synucleinopathies | Drug: 18F-PBR06;Radiation: 18F-PBR06 | Brigham and Women's Hospital | NULL | Not yet recruiting | 18 Years | N/A | All | 50 | NULL | |
7 | EUCTR2022-000336-28-DE (EUCTR) | 12/12/2022 | 28/07/2022 | A Study to evaluate Efficacy, Safety, Tolerability and Effects of TAK-341 in the human body in patients with Multiple System Atrophy A Study to evaluate Efficacy, Safety, Tolerability and Effects of TAK-341 in the human body in patie ... | A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous TAK-341 in Subjects With Multiple System Atrophy A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy, Safety, Tole ... | Multiple System Atrophy MedDRA version: 21.1;Level: PT;Classification code 10064060;Term: Multiple system atrophy;System Organ Class: 10029205 - Nervous system disorders;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] Multiple System Atrophy MedDRA version: 21.1;Level: PT;Classification code 10064060;Term: Multiple s ... | Product Name: TAK-341 Product Code: TAK-341 INN or Proposed INN: Not assigned Other descriptive name: Human IgG1 monoclonal antibody against alpha-synuclein Product Name: TAK-341 Product Code: TAK-341 INN or Proposed INN: Not assigned Other descriptive name: H ... | Takeda Development Center Americas, Inc. | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 138 | Phase 2 | United Kingdom;Italy;Japan;Denmark;Austria;Germany;Portugal;France;United States;Spain | ||
8 | NCT05526391 (ClinicalTrials.gov) | November 9, 2022 | 1/9/2022 | A Study of TAK-341 in Treatment of Multiple System Atrophy | A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy, Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of Intravenous TAK-341 in Subjects With Multiple System Atrophy A Randomized, Double-blind, Placebo-Controlled, Phase 2 Study to Evaluate the Efficacy, Safety, Tole ... | Multiple System Atrophy | Drug: TAK-341;Drug: Placebo | Takeda | AstraZeneca | Recruiting | 40 Years | N/A | All | 138 | Phase 2 | United States;Austria;Denmark;France;Germany;Italy;Japan;Portugal;Spain;United Kingdom |
9 | NCT05698017 (ClinicalTrials.gov) | November 7, 2022 | 16/1/2023 | Study to Evaluate Investigational Allogeneic Cell Therapy Product hOMSC300 for Treatment of Early- to Moderate Stage MSA Study to Evaluate Investigational Allogeneic Cell Therapy Product hOMSC300 for Treatment of Early- t ... | Phase 1/2a Randomized Controlled Study for Treatment of Early- to Moderate Stage Multiple System Atrophy Patients With the Investigational Allogeneic Cell Therapy Product, hOMSC300 Phase 1/2a Randomized Controlled Study for Treatment of Early- to Moderate Stage Multiple System Atr ... | Multiple System Atrophy;MSA - Multiple System Atrophy | Drug: hOMSC300;Other: Sham Procedure | Cytora Ltd. | NULL | Recruiting | 50 Years | 80 Years | All | 18 | Phase 1/Phase 2 | Israel |
10 | NCT04165486 (ClinicalTrials.gov) | July 21, 2022 | 14/11/2019 | Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ION464 Administered to Adults With Multiple System Atrophy (HORIZON) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of ION464 Administered to Adults Wi ... | A Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of ION464 Administered Intrathecally to Adults With Multiple System Atrophy A Phase 1 Study to Assess the Safety, Tolerability, and Pharmacokinetics of ION464 Administered Intr ... | Multiple System Atrophy | Drug: ION464;Drug: Placebo | Ionis Pharmaceuticals, Inc. | NULL | Recruiting | 40 Years | 70 Years | All | 40 | Phase 1 | Austria;France;Germany;United Kingdom;Portugal |