113. 筋ジストロフィー
[臨床試験数:567,薬物数:442(DrugBank:93),標的遺伝子数:55,標的パスウェイ数:151

Searched query = "Muscular dystrophy", "Dystrophinopathies", "Myotilinopathy", "Laminopathy", "Caveolinopathy", "LGMD1C", "Desminopathy", "Sarcoglycanopathy", "α-dystroglycanopathy", "FCMD", "Walker-Warburg syndrome", "Muscle-eye-brain disease", "Myotonic dystrophy", "Integrin α7 deficient CMD", "Rigid spine syndrome"
The queries were searched in Public_title, Scientific_title, and Condition. Export date: 03/15/2021. Trials are sorted by Date_enrollment from most recent to oldest in the table.

Search in Page e.g. "Phase 3", "Not recruiting", "Japan"
2 trials found
No.TrialIDDate_
enrollment
Date_
registration
Public_titleScientific_titleConditionInterventionPrimary_
sponsor
Secondary_
sponsor
Recruitment_
Status
Inclusion_
agemin
Inclusion_
agemax
Inclusion_
gender
Target_
size
PhaseCountries
1NCT00243789
(ClinicalTrials.gov)
September 200521/10/2005Study of Daily Pentoxifylline as a Rescue Treatment in Duchenne Muscular DystrophyA Double-Blinded Randomized Placebo Controlled Study of Daily Pentoxifylline as a Rescue Treatment in DMDMuscular Dystrophy, DuchenneDrug: PentoxifyllineCooperative International Neuromuscular Research GroupNULLCompleted7 YearsN/AMale64Phase 1/Phase 2United States;Argentina;Australia;Canada;Israel;Italy
2NCT00102453
(ClinicalTrials.gov)
March 200229/1/2005Pentoxifylline in Duchenne Muscular DystrophyAn Open-Label Pilot Study of Pentoxifylline in Steroid-naive Duchenne Muscular DystrophyMuscular Dystrophy, DuchenneDrug: PentoxifyllineCooperative International Neuromuscular Research GroupNULLCompleted4 Years7 YearsMale17Phase 1/Phase 2United States