Antibody Treatment for Advanced Celiac Disease
- Celiac disease is a condition where the immune system attacks the cells of the small intestine. The intestine becomes inflamed and cannot digest food properly. The disease most often causes a reaction to foods that contain gluten. Most people can treat celiac disease with a gluten-free diet. However, some people have digestion problems even on a gluten-free diet. Researchers want to try a new antibody therapy for celiac disease. The treatment may block the immune reaction that causes the disease. They will test this antibody in people who have celiac disease that has not responded to a gluten-free diet.
- To see if antibody therapy is a safe and effective treatment for celiac disease that has not responded to standard treatments.
- Individuals at least 18 years of age who have been on a gluten-free diet for 6 to 12 months but still have symptoms of celiac disease.
- Participants will be screened with a physical exam and medical history. Blood samples will be collected. These samples will help determine if the specific antibody treatment is likely to work.
- Before the start of the study, participants will have a biopsy of the small intestine.
- Participants will receive three doses of the study antibody as injections. These doses will be given 3 weeks apart.
- Treatment will be monitored with blood tests and heart function tests. Participants will also have a second small intestine biopsy within a week after the last dose of the antibody.
Biological: Hu-Mik- Beta-1
|Study Design:||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||Phase I Study of the Humanized Mik-Beta-1 Monoclonal Antibody Directed Toward IL-2/IL-15R Beta (CD122) That Blocks IL-15 Action In Patients With Refractory Celiac Disease|
- safety of Hu MIK Beta 1 in celiac disease pts [ Time Frame: end of week 9 ] [ Designated as safety issue: Yes ]
|Study Start Date:||June 2013|
|Estimated Study Completion Date:||June 2015|
|Estimated Primary Completion Date:||June 2015 (Final data collection date for primary outcome measure)|
Hu-Mik-Beta-1 every 3 weeks
Biological: Hu-Mik- Beta-1
Hu-Mik-Beta-1 every 3 weeks for a total of 3 doses (given on day 1, week 3 and week 6)
Show Detailed Description
Please refer to this study by its ClinicalTrials.gov identifier: NCT01893775
|Contact: Thomas A Waldmann, M.D.||(301) firstname.lastname@example.org|
|United States, Minnesota|
|Mayo Clinic, Rochester||Recruiting|
|Rochester, Minnesota, United States, 55905|
|Contact: Carol Van Dyke 507-266-7842 email@example.com|
|Contact: Deanna Brogan (507) 538-1206 firstname.lastname@example.org|
|Principal Investigator:||Thomas A Waldmann, M.D.||National Cancer Institute (NCI)|