Traitements2programmes
Essais1liés
Publications2liées
SourceDBlocale

Traitements

2
MoléculeIndication / populationPhaseObjectifPaysRésultat
HB-adMSCsThis individual patient expanded access IND is requested for a patient diagnosed with LMNA-related congenital muscular dystrophy (L-CMD). In this expanded access, the patient will receive the investigational product through 14 intravenous infusions, followed by Follow-Up visit and an End of Study. Myopathies À vérifier À vérifier United States À vérifier
HB-adMSCsThis individual patient expanded access IND is requested for a patient diagnosed with LMNA-related congenital muscular dystrophy (L-CMD). In this expanded access, the patient will receive the investigational product through 14 intravenous infusions, followed by Follow-Up visit and an End of Study. Myopathies À vérifier À vérifier United States À vérifier

Essais cliniques

1
MoléculeIndication / populationPhaseNCTTitreStatut
HB-adMSCs Myopathies À vérifier NCT05154851 HBCMD01- Expanded Access for the Treatment of Congenital Muscular Dystrophy. NO_LONGER_AVAILABLE

Publications

2
MoléculeIndication / populationTitreJournalDate
HB-adMSCs Autologous adipose-derived mesenchymal stromal cells for chronic traumatic brain injury. Brain : a journal of neurology
HB-adMSCs Evaluation of Multiple Intravenous Infusions of Autologous Adipose-Derived Mesenchymal Stem Cells in Parkinson's Disease: A Randomized, Double-Blind Clinical Trial. Parkinson's disease