Fampridine-SR
( DrugBank: Fampridine / KEGG DRUG: Dalfampridine )
1 disease
告示番号 | 疾患名(ページ内リンク) | 臨床試験数 |
---|---|---|
13 | 多発性硬化症/視神経脊髄炎 | 8 |
13. 多発性硬化症/視神経脊髄炎
臨床試験数 : 3,340 / 薬物数 : 2,163 - (DrugBank : 383) / 標的遺伝子数 : 241 - 標的パスウェイ数 : 238
Showing 1 to 8 of 8 trials
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 | NCT01656148 (ClinicalTrials.gov) | June 201220120600 | 31/7/201220120731 | FAME - Fampyra Outcome Measures Study: a Study of Different Outcome Measures on the Effect of Fampyra FAME - Fampyra Outcome Measures Study: a Study of Different Outcome Measures on the Effect of Fampyr ... | Fampyra Outcome Measures Study: a Study of Different Outcome Measures on the Effect of Fampyra | Multiple Sclerosis | Drug: Fampridine-SR | University of Southern Denmark | Region of Southern Denmark;Biogen | Completed | 18 Years | 60 Years | All | 108 | Phase 4 | Denmark |
2 | NCT01235221 (ClinicalTrials.gov) | December 201020101200 | 4/11/201020101104 | Open Label Extension Study to Evaluate the Safety and Tolerability of Oral Fampridine-Sustained Release (SR) in Canadian Participants With Multiple Sclerosis Who Participated in Acorda Extension Trials. Open Label Extension Study to Evaluate the Safety and Tolerability of Oral Fampridine-Sustained Rele ... | Open-Label Extension Study to Evaluate the Safety and Tolerability of Oral Fampridine SR in Canadian Subjects With Multiple Sclerosis Who Participated in Acorda Extension Trials Open-Label Extension Study to Evaluate the Safety and Tolerability of Oral Fampridine SR in Canadian ... | Multiple Sclerosis | Drug: BIIB041 (Fampridine-SR) | Biogen Idec | Acorda Therapeutics | Completed | 18 Years | 70 Years | Both | 38 | Phase 3 | Canada |
3 | NCT00649792 (ClinicalTrials.gov) | August 200720070800 | 28/3/200820080328 | Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis Who Participated in the MS-F204 Trial Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SRin ... | Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis Who Participated in the MS-F204 Trial Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Famprid ... | Multiple Sclerosis | Drug: Fampridine-SR | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 214 | Phase 3 | United States;Canada |
4 | NCT00483652 (ClinicalTrials.gov) | May 200720070500 | 6/6/200720070606 | Study of Fampridine-SR Tablets in Multiple Sclerosis Patients | Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampridine-SR (10 mg b.i.d. [Bis in Die, Twice Daily]) in Patients With Multiple Sclerosis Double-Blind, Placebo-Controlled, Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampr ... | Multiple Sclerosis | Drug: Fampridine-SR;Drug: Placebo | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 240 | Phase 3 | United States;Canada |
5 | NCT00648908 (ClinicalTrials.gov) | June 200620060600 | 28/3/200820080328 | Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR Tablets in Multiple Sclerosis Patients Who Participated in the MS-F203 Trial Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SRTa ... | Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Subjects With Multiple Sclerosis Who Participated in the MS-F203 Trial Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Famprid ... | Multiple Sclerosis | Drug: Fampridine-SR | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 269 | Phase 3 | United States;Canada |
6 | NCT00127530 (ClinicalTrials.gov) | May 200520050500 | 4/8/200520050804 | Study of Oral Fampridine-SR in Multiple Sclerosis | Double-Blind, Placebo-Controlled, 21-Week, Parallel Group Study to Evaluate Safety and Efficacy of Oral Fampridine-SR in Subjects With Multiple Sclerosis Double-Blind, Placebo-Controlled, 21-Week, Parallel Group Study to Evaluate Safety and Efficacy of O ... | Multiple Sclerosis | Drug: Fampridine-SR;Drug: Placebo | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 300 | Phase 3 | United States;Canada |
7 | NCT00654927 (ClinicalTrials.gov) | November 200320031100 | 4/4/200820080404 | Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SRin ... | Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients With Multiple Sclerosis Phase 3 Open-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Famprid ... | Multiple Sclerosis | Drug: Fampridine-SR b.i.d. (Twice Daily) | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 177 | Phase 3 | United States;Canada |
8 | NCT00053417 (ClinicalTrials.gov) | February 200320030200 | 29/1/200320030129 | Safety and Efficacy Study of Oral Fampridine-SR in Patients With Multiple Sclerosis | Double-Blind, Placebo-Controlled, 20-Week, Parallel Group Study to Evaluate Safety, Tolerability and Activity of Oral Fampridine-SR in Subjects With Multiple Sclerosis Double-Blind, Placebo-Controlled, 20-Week, Parallel Group Study to Evaluate Safety, Tolerability and ... | Multiple Sclerosis | Drug: Placebo;Drug: 10 milligram (mg) fampridine-SR (4-aminopyridine, 4-AP);Drug: 15 mg fampridine-SR (4-aminopyridine, 4-AP);Drug: 20 mg fampridine-SR (4-aminopyridine, 4-AP) Drug: Placebo;Drug: 10 milligram (mg) fampridine-SR(4-aminopyridine, 4-AP);Drug: 15 mg fampridine-SR ... | Acorda Therapeutics | NULL | Completed | 18 Years | 70 Years | All | 206 | Phase 2 | United States;Canada |