Overview

Study of Treatment Response on IgG4 Related Disease (IgG4RD)

Status:
Unknown status
Trial end date:
2018-06-01
Target enrollment:
0
Participant gender:
All
Summary
This is an open-label randomized controlled trial to compare the efficacy of Prednisone alone and combination therapy of Prednisone and Mycophenolate mofetil in IgG4RD patients.
Phase:
Phase 2
Accepts Healthy Volunteers?
No
Details
Lead Sponsor:
Peking Union Medical College Hospital
Treatments:
Immunoglobulin G
Mycophenolate mofetil
Mycophenolic Acid
Prednisolone
Prednisone
Criteria
Inclusion Criteria:

- Males and females

- Aged 18 to 70 years old with informed consent

- All patients must meet the following diagnostic criteria of IgG4RD (2011):

1. swelling, sclerosing and inflammatory involvement of one or more organ, including
sclerosing pancreatitis, sialadenitis (Mikulicz disease), sclerosing cholangitis,
inflammatory pseudotumors, retroperitoneal or mediastinal fibrosis, interstitial
nephritis, hypophysitis, sclerosing dacryoadenitis, inflammatory aortic aneurysm,
lymphadenopathy, or other inflammatory conditions;

2. elevated serum IgG4 (>1.35 g/L);

3. histopathologic features of fibrosis and/or lymphocytic and polyclonal plasma
cell infiltration (and IgG4+ plasma cells on immunohistology when performed).
Patients fulfill 1)+2)+3) are diagnosed as definite IgD4RD, 1)+2): possible
IgG4RD; 1)+3): probable IgG4RD;

4. exclusion of other diseases.

Exclusion Criteria:

- Patients will not be included if meets any of the following criteria:

1. Patients who were diagnosed as other autoimmune diseases;

2. Patients who were diagnosed as malignant diseases;

3. Pregnant and lactating women;

4. Active infection: HIV, HCV, HBV, TB;

5. Serious organ function failure, expected life time less than 6 months.

6. Presenting with Mikulicz disease without other manifestations.