Title

An Australian Study of Mesenchymal Stromal Cells for Crohn's Disease
A Multicentre Australian Phase 2 Study to Evaluate Safety and Efficacy of Mesenchymal Stromal Cells for Treating Biologic Refractory Crohn's Disease
  • Phase

    Phase 2
  • Study Type

    Interventional
  • Status

    Completed No Results Posted
  • Study Participants

    21
Despite the advent of newer biologic therapies such as infliximab for Crohn's disease, a form of autoimmune inflammatory bowel disease, a proportion of patients are refractory to such therapy and require surgery. The hypothesis is that mesenchymal stromal cell therapy using third party human cultured cells will be safe and effective
Study Started
Jan 31
2010
Primary Completion
Jun 30
2014
Study Completion
Jun 30
2015
Last Update
Jun 09
2015
Estimate

Drug Mesenchymal stromal cells (MSC) for infusion

MSC 2X10E6/kg recipient weight are infused over 15 minutes intravenously weekly for 4 weeks

  • Other names: No other names

Mesenchymal stromal cells Experimental

Mesenchymal stromal cells administered weekly for 4 weeks

Criteria

Inclusion Criteria:

Colonic or small bowel Crohn's disease based on endoscopic appearances and histology
Refractory to induction with infliximab or adalimumab; or have lost response to these agents; or have had side effects precluding their further use
Where there has been loss of response to one of these agents, the other must be tried before being eligible
Crohn's disease activity score (CDAI) 250 or more.
C-reactive protein >10mg/L
Surgery must have been offered to the subject (if appropriate) and declined
Signed informed consent

Exclusion Criteria:

Active sepsis, perforating disease. Coexistent perianal fistulous disease is permitted, providing no co-existent infection within previous 4 weeks
Chronic stricturing disease in isolation
Coexistent CMV disease
Prior history of malignancy
Pregnant or unwilling to practice contraceptive therapy or breast feeding females
Last biologic therapy must be greater than 4 weeks prior, must be on stable corticosteroid dose for 14 days prior, during therapy and for 14 days after therapy, must be on stable immunomodulator dose (eg, azathioprine) for 14 days prior, during therapy and for 14 days after.
No Results Posted