Evaluation of PROCHYMAL® Adult Human Stem Cells for Treatment-resistant Moderate-to-severe Crohn's Disease
Launched by MESOBLAST, INC. · May 31, 2007
Trial Information
Current as of May 08, 2025
Completed
Keywords
ClinConnect Summary
A significant number of individuals with Crohn's disease do not find relief with existing steroidal, immunosuppressive, or biologic therapies, and are forced to seek surgery or other drastic measures for treatment.
PROCHYMAL® adult human stem cells are manufactured from healthy, volunteer donors, extensively tested, and are stored to be available as needed. Human and animal studies have shown that the cells do not require any donor-recipient matching. The cells may have both immunosuppressive and healing benefits in Crohn's disease. The cells naturally migrate specifically to sites of infl...
Gender
ALL
Eligibility criteria
- Inclusion Criteria:
- • failed (within last 2 yr) or intolerant of at least one steroid AND at least one immunosuppressant AND at EXACTLY one biologic
- • CDAI between 250 and 450, inclusive
- • endoscopically or radiographically confirmed Crohn's disease of ileus or colon or both
- • C-Reactive Protein Test (CRP) of at least 5 mg/l (0.5 mg/dl)\*OR\* CDAI of at least 300
- • weight between 40 and 150 kg, inclusive
- • adequate renal function
- • negative tuberculosis skin (PPD) test (or evaluated low risk of TB activation)
- Exclusion Criteria:
- • HIV or hepatitis infection active
- • allergy to CT contrast agents, or to bovine or porcine products
- • symptomatic fibrostenotic Crohn's disease
- • permanent ostomy
- • biologic therapy within past 90 d
- • prednisone greater than 20 mg/d within past month
- • short-bowel syndrome
- • total parenteral nutrition
- • abnormal liver function
- • malignancy active within past 5 years (except completely resected basal or squamous cell carcinoma of skin)
- • enteric pathogens, including C. difficile
- • history of colonic mucosal dysplasia
- • current or prior evidence of tuberculosis (TB) (unless risk of activation or re-activation deemed low)
About Mesoblast, Inc.
Mesoblast, Inc. is a leading regenerative medicine company focused on developing innovative cellular therapies to address unmet medical needs across various therapeutic areas, including orthopedic, cardiovascular, and autoimmune diseases. With a strong emphasis on harnessing the potential of allogeneic mesenchymal stem cells, Mesoblast aims to provide transformative treatment options that improve patient outcomes and quality of life. The company is committed to advancing its robust pipeline of clinical programs through rigorous research and development, collaboration with key stakeholders, and adherence to the highest standards of regulatory compliance.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Burlington, Vermont, United States
Pittsburgh, Pennsylvania, United States
San Francisco, California, United States
Boston, Massachusetts, United States
Lebanon, New Hampshire, United States
Calgary, Alberta, Canada
New York, New York, United States
Winston Salem, North Carolina, United States
Urbana, Illinois, United States
Louisville, Kentucky, United States
Toronto, Ontario, Canada
Dallas, Texas, United States
Rochester, New York, United States
Nashville, Tennessee, United States
Boston, Massachusetts, United States
Bethesda, Maryland, United States
Galveston, Texas, United States
Chicago, Illinois, United States
Adelaide, South Australia, Australia
Indianapolis, Indiana, United States
Tulsa, Oklahoma, United States
Clearwater, Florida, United States
Richmond, Virginia, United States
Atlanta, Georgia, United States
Norfolk, Virginia, United States
London, Ontario, Canada
Chevy Chase, Maryland, United States
Winter Park, Florida, United States
Rochester, New York, United States
Charlotte, North Carolina, United States
Worcester, Massachusetts, United States
Baltimore, Maryland, United States
Jacksonville, Florida, United States
Winnipeg, Manitoba, Canada
Los Angeles, California, United States
Wheat Ridge, Colorado, United States
Hamilton, , New Zealand
Houston, Texas, United States
Lexington, Kentucky, United States
Troy, Michigan, United States
Seattle, Washington, United States
Edmonton, Alberta, Canada
Topeka, Kansas, United States
Baton Rouge, Louisiana, United States
Dearborn, Michigan, United States
Minneapolis, Minnesota, United States
Saint Louis, Missouri, United States
New York, New York, United States
Stony Brook, New York, United States
Pinehurst, North Carolina, United States
Tulsa, Oklahoma, United States
Pittsburgh, Pennsylvania, United States
Germantown, Tennessee, United States
Nashville, Tennessee, United States
Melbourne, Victoria, Australia
Christchurch, , New Zealand
Patients applied
Trial Officials
Mahboob Rahman, MD
Study Director
Mesoblast, Inc.
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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