8. ハンチントン病 Huntington disease Clinical trials / Disease details
臨床試験数 : 242 / 薬物数 : 205 - (DrugBank : 62) / 標的遺伝子数 : 85 - 標的パスウェイ数 : 159
Showing 1 to 10 of 242 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 | NCT05686551 (ClinicalTrials.gov) | January 30, 2023 | 16/12/2022 | GENERATION HD2. A Study to Evaluate the Safety, Biomarkers, and Efficacy of Tominersen Compared With Placebo in Participants With Prodromal and Early Manifest Huntington's Disease. GENERATION HD2. A Study to Evaluate the Safety, Biomarkers, and Efficacy of Tominersen Compared With ... | A Phase II, Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Study to Evaluate the Safety, Biomarkers, and Efficacy of Tominersen in Individuals With Prodromal and Early Manifest Huntington's Disease A Phase II, Randomized, Double-Blind, Placebo-Controlled, Dose-Finding Study to Evaluate the Safety, ... | Huntington Disease | Drug: Tominersen 60 mg;Drug: Placebo;Drug: Tominersen 100 mg | Hoffmann-La Roche | NULL | Recruiting | 25 Years | 50 Years | All | 360 | Phase 2 | United States;Spain |
2 | EUCTR2022-001991-32-ES (EUCTR) | 22/12/2022 | 23/12/2022 | A Study to Evaluate the Safety, Biomarkers, and Efficacy of Tominersen in Individuals with Prodromal and Early Manifest Huntington’s Disease A Study to Evaluate the Safety, Biomarkers, and Efficacy of Tominersen in Individuals with Prodromal ... | A PHASE II, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, BIOMARKERS, AND EFFICACY OF TOMINERSEN IN INDIVIDUALS WITH PRODROMAL AND EARLY MANIFEST HUNTINGTON’S DISEASE A PHASE II, RANDOMIZED, DOUBLE-BLIND, PLACEBO-CONTROLLED, DOSE-FINDING STUDY TO EVALUATE THE SAFETY, ... | Huntington's disease (HD) MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntington's disease;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Huntington's disease(HD) MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntingto ... | Product Code: RO7234292 INN or Proposed INN: Tominersen Other descriptive name: N/A | Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La Roche Ltd Roche Farma S. A. U. que realiza el ensayo en España y que actúa como representante F. Hoffmann-La R ... | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 360 | Phase 2 | Canada;Argentina;Spain;Australia;United Kingdom;New Zealand;Japan | ||
3 | NCT05655520 (ClinicalTrials.gov) | December 14, 2022 | 9/12/2022 | A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Huntington's Disease A Study to Evaluate the Safety and Tolerability of SAGE-718 in Participants With Huntington's Diseas ... | A Phase 3, Multicenter, Open-label Safety Study to Evaluate the Long-term Safety and Tolerability of SAGE-718 in Participants With Huntington's Disease A Phase 3, Multicenter, Open-label Safety Study to Evaluate the Long-term Safety and Tolerability of ... | Huntington Disease | Drug: SAGE-718 | Sage Therapeutics | NULL | Recruiting | 25 Years | 65 Years | All | 300 | Phase 3 | United States |
4 | NCT05541627 (ClinicalTrials.gov) | October 12, 2022 | 13/9/2022 | A Study to Evaluate AB-1001 Striatal Administration in Adults With Early Manifest Huntington's Disease A Study to Evaluate AB-1001 Striatal Administration in Adults With Early Manifest Huntington's Disea ... | An Open-Label Phase I/II Dose Finding Study to Evaluate the Safety, Tolerability, and Preliminary Efficacy of Striatal Administration of AB-1001 in Adult Subjects With Early Manifest Huntington's Disease (HD) An Open-Label Phase I/II Dose Finding Study to Evaluate the Safety, Tolerability, and Preliminary Ef ... | Huntington Disease | Genetic: AB-1001 Gene Therapy | Brainvectis, a subsidiary of Asklepios BioPharmaceutical, Inc. (AskBio) | NULL | Recruiting | 18 Years | 65 Years | All | 18 | Phase 1/Phase 2 | France |
5 | NCT05475483 (ClinicalTrials.gov) | August 2, 2022 | 22/7/2022 | Efficacy and Safety on SOM3355 in Huntington's Disease Chorea | Phase IIb, Randomized, Double-blind, Placebo-controlled Study in Parallel Groups Assessing the Efficacy and Safety of Two Doses of SOM3355 in Patients Suffering From Huntington's Disease With Choreic Movements Phase IIb, Randomized, Double-blind, Placebo-controlled Study in Parallel Groups Assessing the Effic ... | Huntington Chorea | Drug: SOM3355 capsules;Drug: Placebo capsules | SOM Innovation Biotech SA | NULL | Recruiting | 21 Years | N/A | All | 129 | Phase 2 | France;Germany;Italy;Poland;Spain;Switzerland;United Kingdom |
6 | EUCTR2021-003052-16-FR (EUCTR) | 20/07/2022 | 08/12/2021 | Phase I/II Safety and Tolerability Study of striatal administration of BV-101 in adult subjects with Early Manifest Huntington's Disease (HD) Phase I/II Safety and Tolerability Study of striatal administration of BV-101 in adult subjects with ... | An Open-Label Phase I/II Dose Finding Study to evaluate the Safety, Tolerability, and Preliminary Efficacy of Striatal Administration of BV-101 in Adult Subjects with Early Manifest Huntington's Disease (HD) An Open-Label Phase I/II Dose Finding Study to evaluate the Safety, Tolerability, and Preliminary Ef ... | Huntington's disease MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntington's disease;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] Huntington's disease MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntington's ... | Product Name: AAVrh10.CAG.hCYP46A1 Product Code: BV-101 INN or Proposed INN: AAVrh10.CAG.hCYP46A1 Other descriptive name: ADENO-ASSOCIATED VIRAL VECTOR SEROTYPE RH10 CONTAINING THE HUMAN CHOLESTEROL 24-HYDROXYLASE GENE Product Name: AAVrh10.CAG.hCYP46A1 Product Code: BV-101 INN or Proposed INN: AAVrh10.CAG.hCYP46A1 Other ... | Brainvectis | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 18 | Phase 1;Phase 2 | United States;France | ||
7 | NCT05358821 (ClinicalTrials.gov) | June 22, 2022 | 27/4/2022 | A Study to Evaluate the Effect of SAGE-718 on Functioning Capacity in Participants With Huntington's Disease A Study to Evaluate the Effect of SAGE-718 on Functioning Capacity in Participants With Huntington's ... | A 28-Day Randomized, Placebo-Controlled, Double-Blind, Parallel Groups and Normative Comparison Study to Evaluate the Effect of SAGE-718 on Functioning Capacity in Participants With Huntington's Disease A 28-Day Randomized, Placebo-Controlled, Double-Blind, Parallel Groups and Normative Comparison Stud ... | Huntington Disease | Drug: SAGE-718;Drug: Placebo | Sage Therapeutics | NULL | Recruiting | 25 Years | 65 Years | All | 80 | Phase 2 | United States |
8 | NCT04478734 (ClinicalTrials.gov) | June 1, 2022 | 11/2/2020 | Trial of the Combined Use of Thiamine and Biotin in Patients With Huntington's Disease | Multicentric Trial on the Use of Combined Therapy of Thiamine and Biotine in Patients With Huntington´s Disease Multicentric Trial on the Use of Combined Therapy of Thiamine and Biotine in Patients With Huntingto ... | Huntington Disease | Drug: Moderate doses of Thiamine y Biotin;Drug: High doses of Thiamine y Biotin | Fundación Pública Andaluza para la gestión de la Investigación en Sevilla | Ciberned (Centro de Investigación Biomédica en Red) | Not yet recruiting | 18 Years | N/A | All | 24 | Phase 2 | Spain |
9 | EUCTR2021-003852-18-DE (EUCTR) | 06/05/2022 | 18/02/2022 | A Phase 2A study of PTC518 in patients with Huntington's Disease | A PHASE 2A, RANDOMIZED, PLACEBO-CONTROLLED, DOSE-RANGING STUDY TO EVALUATE THE SAFETY AND EFFICACY OF PTC518 IN SUBJECTS WITH HUNTINGTON'S DISEASE - PIVOT-HD A PHASE 2A, RANDOMIZED, PLACEBO-CONTROLLED, DOSE-RANGING STUDY TO EVALUATE THE SAFETY AND EFFICACY O ... | Huntington’s disease MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntington's disease;System Organ Class: 10010331 - Congenital, familial and genetic disorders;Therapeutic area: Diseases [C] - Congenital, Hereditary, and Neonatal Diseases and Abnormalities [C16] Huntington’s disease MedDRA version: 20.0;Level: PT;Classification code 10070668;Term: Huntington's ... | Product Name: PTC518 tablet 5 mg Product Code: PTC518 INN or Proposed INN: Not available Other descriptive name: PTC518 Product Name: PTC518 tablet 20 mg Product Code: PTC518 INN or Proposed INN: Not available Other descriptive name: PTC518 Product Name: PTC518tablet 5 mg Product Code: PTC518 INN or Proposed INN: Not available Other descripti ... | PTC Therapeutics, INC | NULL | Authorised-recruitment may be ongoing or finished | Female: yes Male: yes | 162 | Phase 2 | France;United States;Australia;Netherlands;Germany;United Kingdom | ||
10 | NCT05358717 (ClinicalTrials.gov) | April 25, 2022 | 27/4/2022 | A Study to Evaluate the Safety and Efficacy of PTC518 in Participants With Huntington's Disease (HD) | A Phase 2A, Randomized, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety and Efficacy of PTC518 in Subjects With Huntington's Disease A Phase 2A, Randomized, Placebo-Controlled, Dose-Ranging Study to Evaluate the Safety and Efficacy o ... | Huntington Disease | Drug: PTC518;Drug: Placebo | PTC Therapeutics | NULL | Recruiting | 25 Years | N/A | All | 162 | Phase 2 | United States;Australia;France;Germany;Netherlands;United Kingdom |