113. Muscular dystrophy Clinical trials / Disease details


Clinical trials : 622 Drugs : 485 - (DrugBank : 99) / Drug target genes : 59 - Drug target pathways : 168

  
2 trials found
No.TrialIDDate_
enrollment
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registration
Public_titleScientific_titleConditionInterventionPrimary_
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agemin
Inclusion_
agemax
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gender
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PhaseCountries
1EUCTR2004-000622-67-GB
(EUCTR)
03/06/200510/02/2005A Double-Blind, Placebo-Controlled, Randomized, Multiple Ascending Dose, Safety Study of MYO-029 Administered to Adult Patients with Becker, Facioscapulohumeral and Limb-Girdle Muscular Dystrophy.A Double-Blind, Placebo-Controlled, Randomized, Multiple Ascending Dose, Safety Study of MYO-029 Administered to Adult Patients with Becker, Facioscapulohumeral and Limb-Girdle Muscular Dystrophy. Becker Muscular Dystrophy, Facioscapulohumeral Muscular Dystrophy, Limb-Girdle Muscular Dystrophy.Product Name: MYO-029
INN or Proposed INN: Not Available
Other descriptive name: Recombinant human anti-GDF-8 antibody
Wyeth Research Division of Wyeth Pharmaceuticals Inc.NULLNot Recruiting Female: yes
Male: yes
136 Human pharmacology (Phase 1): no Therapeutic exploratory (Phase 2): yes Therapeutic confirmatory - (Phase 3): no Therapeutic use (Phase 4): noUnited Kingdom
2NCT00104078
(ClinicalTrials.gov)
February 200522/2/2005Study Evaluating MYO-029 in Adult Muscular DystrophyBecker Muscular Dystrophy;Facioscapulohumeral Muscular Dystrophy;Limb-Girdle Muscular DystrophyDrug: MYO-029Wyeth is now a wholly owned subsidiary of PfizerNULLCompleted18 YearsN/ABoth108Phase 1/Phase 2United States