NCT07595367

Evaluate the Effectiveness and Safety of BBD-1 Multi-target Immune Enhancement Targeting Agent in the Treatment of Hypersensitivity Reaction (IgA) Vasculitis

Enrolling by Invitation
PHASE2All AgesInterventionalTreatment
Qifeng Zhang
~30 participants
Updated 2026-05-19 on ClinicalTrials.gov
What's tested:BBD-1 Multi target Immune Enhancement Targeting Agent

At a glance

Recruiting sites
0 of 2 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Allergic reaction (IgA) vasculitis
Measured over 7 days
Allergic Reaction (IgA) Vasculitis
2 sites across 2 states
Maryland1
Shandong1

This trial hasn't published a contact. View it on ClinicalTrials.gov

  • Allergic reaction (IgA) vasculitis7 days

    1. The disappearance of palpable purpura is a direct manifestation of recovery. Observe whether there are new subcutaneous bleeding points on the patient's body, and whether the original purpura color gradually changes from purple red to yellow brown until it disappears. Some patients may have temporary pigmentation, but it will not continue to expand or recur. 2. Joint pain disappears. Patients with hypersensitivity reaction (IgA) vasculitis answered in the questionnaire that the swollen joint pain was relieved and their mobility was restored, indicating that the inflammation was under control. Diagnosis can also be made through C-reactive protein testing. 3. No proteinuria (24-hour urine protein below 0.4g/24 hours). Urine routine examination can detect protein indicators in urine to evaluate kidney function. 4. The serum albumin level is 35g-55g/L. Serum creatinine is below 1.24mg/dL. Perform blood biochemical tests on serum albumin and serum creatinine to evaluate renal function.