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Clinical Trials in China / NCT06663618
Recruiting Not applicable

Short-term Glucocorticoid Combined with MMF for IgG4-RD

NCT06663618 · tracked via the Priya Life Science China tracker
Sponsor
Wen Zhang
Phase
Not applicable
Started
2023-09-01
Last updated
2024-10-29

Condition(s) studied

IgG4-related Disease

Investigational drug(s) / intervention(s)

prednisonMycophenolate mofetil

prednison: Oral prednison starts at 0.6-0.8mg/kg/d, then tapered and withdrawal in 6 months.

Mycophenolate mofetil: Oral Mycophenolate mofetil 0.75g bid for 6 months.

Study summary

Comparison of short-term glucocorticoid monotherapy and short-term glucocorticoid combined with MMF in the treatment of IgG4 Related Disease

Eligibility

Sex
ALL
Min age
18 Years
Max age
80 Years
Healthy volunteers
No
Inclusion Criteria: 1. 18-80 years old; 2. All patients must meet the comprehensive diagnostic criteria of IgG4-RD revised in Japan in 2020 or the classification criteria of IgG4-RD formulated by ACR/EULAR in 2019; 3. Active IgG4-RD (at least one organ has an IgG4-RD reaction score \>=2 at the time of enrollment.); 4. No previous medication or recurrence after withdrawal. Exclusion Criteria: 1. Combined with other autoimmune diseases as the main diagnosis. 2. Pregnant or lactating women 3. Patients with malignant tumor 4. Active bacterial, fungal, viral or mycobacterial infections. 5. Severe complications of important organs, and the expected survival time is less than 6 months.

Primary outcome measure(s)

Trial sites (1)

FacilityCityRegionStatus
Peking Union Medical College Hospital Beijing Beijing Municipality Recruiting

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06663618 on ClinicalTrials.gov ↗ ← All trials in China