Celulas madre mesenquimales troncales adultas alogenicas de médula ósea no expandida ( DrugBank: - )


1 disease
IDDisease name (Link within this page)Number of trials
274Osteogenesis Imperfecta1

274. Osteogenesis Imperfecta


Clinical trials : 91 Drugs : 101 - (DrugBank : 20) / Drug target genes : 11 - Drug target pathways : 48
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agemin
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agemax
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PhaseCountries
1EUCTR2012-002553-38-ES
(EUCTR)
09/08/201309/04/2013Mesenchymal stem cell based therapy for the treatment of osteogenesis imperfectaMesenchymal stem cell based therapy for the treatment of osteogenesis imperfecta - TERCELOI Osteogenesis imperfecta (OI) is a rare genetic disorder with increased bone fragility of varying severity. In the majority of patients the disease is caused by mutations in collagen type I. Severe OI is characterized by osteopenia, frequent fractures, progressive deformity, short stature, loss of mobility, chronic pain and can lead to premature death. At present a cure does not exist.;Therapeutic area: Body processes [G] - Cell Physiological Phenomena [G04]Product Name: celulas madre mesenquimales troncales adultas alogenicas de médula ósea no expandida
Product Code: REF CRUZADA PEI Nº 12-088
INN or Proposed INN: células mesenquimales troncales adultas alogénicas de médula ósea no expandidas
Other descriptive name: células mesenquimales troncales adultas alogénicas de médula ósea no expandidas(ref cruzada PEI nº 12-088)
Itziar Astigarraga AguirreNULLAuthorised-recruitment may be ongoing or finishedFemale: yes
Male: yes
Spain