201. アンジェルマン症候群 [臨床試験数:12,薬物数:15(DrugBank:7),標的遺伝子数:22,標的パスウェイ数:20]
Searched query = "Angelman syndrome"
The queries were searched in Public_title, Scientific_title, and Condition of the data. Export date: 11/20/2019, 11/21/2019. Trials are sorted by Date_enrolment from most recent to oldest in the table.
No. | TrialID | Date_ enrollement | Last_Refreshed_ on | 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 | NCT04106557 | September 9, 2019 | 14 October 2019 | A Study of OV101 in Individuals With Angelman Syndrome (AS) | A Multicenter, Randomized, Double-Blind, Placebo-Controlled, Parallel-Group, Phase 3 Study to Evaluate the Efficacy and Safety of OV101 in Pediatric Individuals With Angelman Syndrome | Primary Disease or Condition Being Studied: Angelman Syndrome (AS) | Drug: Gaboxadol;Drug: Placebo | Ovid Therapeutics Inc. | Recruiting | 2 Years | 12 Years | All | 65 | Phase 3 | United States | |
2 | NCT03882918 | February 25, 2019 | 8 April 2019 | An Open-Label Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of OV101 in Individuals With Angelman Syndrome | An Open-Label Study to Evaluate the Long-Term Safety, Tolerability, and Efficacy of OV101 in Individuals With Angelman Syndrome | Angelman Syndrome | Drug: OV101 | Ovid Therapeutics Inc. | Recruiting | 13 Years | 49 Years | All | 82 | Phase 2 | United States | |
3 | NCT03644693 | August 13, 2018 | 3 September 2018 | Nutritional Formulation for Angelman Syndrome | Evaluation of the Safety and Tolerability of a Nutritional Formulation in Angelman Syndrome | Angelman Syndrome | Dietary Supplement: Nutritional Formulation Containing Exogenous Ketones;Dietary Supplement: Placebo Formulation | Vanderbilt University Medical Center | Recruiting | 4 Years | 11 Years | All | 15 | N/A | United States | |
4 | NCT03109756 | April 3, 2017 | 16 December 2017 | Single Dose Pharmacokinetic (PK) Study | A Phase 1 Single Dose PK Study in Adolescent Subjects With Fragile X Syndrome or Angelman Syndrome | Angelman Syndrome;Fragile X Syndrome | Drug: OV101 | Ovid Therapeutics Inc. | Not recruiting | 13 Years | 17 Years | All | 12 | Phase 1 | United States | |
5 | NCT02996305 | January 2016 | 20 August 2018 | A Study in Adults and Adolescents With Angelman Syndrome | A Phase 2 Adult and Adolescent Angelman Syndrome Clinical Trial: A Randomized, Double-Blind, Safety and Efficacy Study of Gaboxadol | Angelman Syndrome | Drug: OV101 Regimen 1;Drug: OV101 regimen 2;Other: Placebo | Ovid Therapeutics Inc. | Not recruiting | 13 Years | 49 Years | All | 88 | Phase 2 | United States;Israel | |
No. | TrialID | Date_ enrollement | Last_Refreshed_ on | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
6 | NCT02056665 | January 2014 | 2 November 2015 | Study to Evaluate the Efficacy and Safety of Minocycline in Angelman Syndrome | Randomized Clinical Trial, Placebo Compared to Evaluate the Efficacy and Safety of Minocycline in Angelman Syndrome | Angelman Syndrome | Drug: MINOCYCLINE;Drug: PLACEBO (for Minocycline) | Puerta de Hierro University Hospital | Not recruiting | 6 Years | 30 Years | Both | 32 | Phase 2 | Spain | |
7 | EUCTR2013-002154-67-ES | 26/12/2013 | 27 January 2014 | STUDY TO EVALUATE THE EFFICACY AND SAFETY OF MINOCYCLINE IN ANGELMAN SYNDROME (A-MANECE STUDY) | RANDOMIZED CLINICAL TRIAL, PLACEBO COMPARED TO EVALUATE THE EFFICACY AND SAFETY OF MINOCYCLINE IN ANGELMAN SYNDROME (A-MANECE STUDY) - A-MANECE | Angelman Syndrome MedDRA version: 16.0 Level: PT Classification code 10049004 Term: Angelman's syndrome System Organ Class: 10010331 - Congenital, familial and genetic disorders ;Therapeutic area: Diseases [C] - Nervous System Diseases [C10] | Trade Name: Aknemin 50 Pharmaceutical Form: Capsule INN or Proposed INN: MINOCYCLINE CAS Number: 13614-98-7 Current Sponsor code: PL 33016/0005 Other descriptive name: MINOCYCLINE HYDROCHLORIDE Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 50- Pharmaceutical form of the placebo: Capsule Route of administration of the placebo: Oral use | Dra. Cristina Avendaño Solá | Authorised | Female: yes Male: yes | Spain | |||||
8 | NCT03235037 | November 26, 2013 | 29 April 2019 | Clinical Trial of Levodopa/Carbidopa ( Sinemet) Therapy in Angel Man Syndrome | Clinical Trial of Levodopa/Carbidopa ( Sinemet) Therapy in Angel Man Syndrome | Angelman Syndrome | Drug: Levodopa | Bennett Lavenstein | Not recruiting | 18 Months | 16 Years | All | 10 | N/A | ||
9 | NCT01531582 | April 2012 | 19 February 2015 | Minocycline in the Treatment of Angelman Syndrome | The Efficacy of Minocycline in the Treatment of Angelman Syndrome | Angelman Syndrome | Drug: minocycline | University of South Florida | Not recruiting | 4 Years | 12 Years | Both | 25 | N/A | United States | |
10 | NCT01281475 | January 2011 | 19 October 2017 | A Trial of Levodopa in Angelman Syndrome | A Phase 2 Randomized Placebo-Controlled Trial of Levodopa in Angelman Syndrome | Angelman Syndrome | Drug: Placebo Oral Capsule;Drug: Levodopa | Wen-Hann Tan | Rady Children's Hospital, San Diego;University of California, San Francisco;Baylor College of Medicine;Vanderbilt University;Greenwood Genetic Center;Children's Hospital Medical Center, Cincinnati;Angelman Syndrome Foundation, Inc. | Not recruiting | 4 Years | 12 Years | All | 67 | Phase 2/Phase 3 | United States |
No. | TrialID | Date_ enrollement | Last_Refreshed_ on | Public_title | Scientific_title | Condition | Intervention | Primary_ sponsor | Secondary_ sponsor | Recruitment_ Status | Inclusion_ agemin | Inclusion_ agemax | Inclusion_ gender | Target_ size | Phase | Countries |
11 | NCT00829439 | January 2009 | 19 October 2017 | Study on Tolerability of Levodopa/Carbidopa in Children With Angelman Syndrome | A Dose-escalation Tolerability Study of Levodopa/Carbidopa in Angelman Syndrome | Angelman Syndrome | Drug: Levodopa/Carbidopa (4:1) | Boston Children’s Hospital | Not recruiting | 4 Years | 12 Years | All | 16 | Phase 1 | United States | |
12 | NCT00348933 | July 2006 | 19 October 2017 | Dietary Supplements for the Treatment of Angelman Syndrome | Efficacy of a Therapeutic Treatment Trial in Angelman Syndrome | Angelman Syndrome;Nervous System Diseases | Drug: Betaine;Drug: Creatine;Drug: Metafolin;Drug: Vitamin B12 | University of California, San Diego | Baylor College of Medicine;Rady Children's Hospital, San Diego;Boston Children’s Hospital;Greenwood Genetic Center;Rare Diseases Clinical Research Network | Not recruiting | N/A | 5 Years | All | 90 | N/A | United States |