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Purpose

The goal of this clinical trial is to learn if efgartigimod can treat IgG4-related disease in adults. The main questions it aims to answer are: In patients with IgG4-related disease, does treatment with efgartigimod reduce the volume of the: - lacrimal gland(s) and/or - salivary gland(s) and/or - pancreas Participants will: - Receive efgartigimod once weekly for up to 12 weeks - Visit the clinic every one to six weeks for checkups and tests - Be asked to complete questionnaires to see how they feel on efgartigimod

Condition

Eligibility

Eligible Ages
Between 18 Years and 90 Years
Eligible Sex
All
Accepts Healthy Volunteers
No

Inclusion Criteria

  • Have a clinical diagnosis of IgG4-related disease that requires treatment in the opinion of the investigator - Meet the 2019 ACR/EULAR Classification Criteria for IgG4-Related Disease - Have a serum IgG4 concentration greater than or equal to 2 times the upper limit of normal at Screening - Have involvement of the lacrimal gland(s), salivary gland(s), and/or pancreas - If lacrimal and/or salivary glands are involved, it must be symptomatic, including but not limited to discomfort, pain, dryness, headache, or vision changes - If the pancreas is involved, it must be asymptomatic, diffuse enlargement without signs or symptoms of obstruction or evidence of major organ dysfunction in the opinion of the investigator - Have a prior inadequate response to, or intolerance of, glucocorticoids, or who have experienced recurrent symptoms after previous treatment with glucocorticoids - Are not receiving current treatment with immunosuppressive medications - All women must test negative for pregnancy and agree to use a reliable method of birth control

Exclusion Criteria

  • Any exclusion criteria listed in the 2019 ACR/EULAR Classification Criteria for IgG4-Related Disease - Prior treatment with an FcRn inhibitor - Have conventional synthetic disease-modifying antirheumatic drug (csDMARD) or immunosuppressive use as follows: - Treatment with glucocorticoids within 28 days prior to Baseline or planned treatment during the study - Treatment with csDMARDs including but not limited to hydroxychloroquine, methotrexate, leflunomide, or sulfasalazine within 28 days prior to Baseline or planned treatment during the study - Treatment with cytotoxic or immunosuppressive drugs including but not limited to cyclophosphamide, mycophenolic acid, azathioprine, cyclosporine, sirolimus, or tacrolimus within 28 days prior to Baseline or planned treatment during the study - Treatment with a janus kinase (JAK) inhibitor including but not limited to tofacitinib, baricitinib, upadacitinib, or filgotinib within 28 days prior to Baseline or planned treatment during the study - Treatment with a Bruton's tyrosine kinase (BTK) inhibitor including but not limited to ibrutinib, zanubrutinib, acalabrutinib, pirtobrutinib, or rilzabrutinib within 28 days prior to Baseline or planned treatment during the study - Have biologic disease-modifying antirheumatic drug (bDMARD) use as follows: - Treatment with etanercept, adalimumab, or anakinra within 28 days before Baseline or planned treatment during the study - Treatment with infliximab, certolizumab pegol, golimumab, abatacept, or tocilizumab within 56 days before Baseline or planned treatment during the study - Treatment with a B cell depleting agent including but not limited to rituximab, ocrelizumab, obinutuzumab, ofatumumab, inebilizumab, ianalumab, or obexelimab ≤ 6 months prior to Baseline - Patients who received B-cell targeted therapy > 6 and ≤ 12 months prior to Baseline must have a B-cell count that is within the laboratory reference range at Screening - Treatment with a BAFF antagonist including but not limited to belimumab or tabalumab within 6 months before Baseline or planned treatment during the study - Treatment with an IL-17 antagonist including but not limited to secukinumab, ixekizumab, or brodalumab within 6 months before Baseline or planned treatment during the study - Prior treatment with other bDMARDs may be allowed at the discretion of the investigator - A history of, or current, inflammatory or autoimmune disease (that could affect the interpretation of safety or efficacy outcomes) other than IgG4-related disease - Evidence of active tuberculosis, HIV, or hepatitis B or C infection - History of cancer except for skin basal or squamous cell carcinoma, cervical dysplasia or carcinoma in situ that has been treated and is considered cured > 1 year prior to Baseline, prostate cancer considered cured for > 5 years with a normal prostate specific antigen, or colon cancer considered cured > 5 years

Study Design

Phase
Phase 2
Study Type
Interventional
Allocation
N/A
Intervention Model
Single Group Assignment
Primary Purpose
Treatment
Masking
None (Open Label)

Arm Groups

ArmDescriptionAssigned Intervention
Experimental
efgartigimod 		Participants will be treated with efgartigimod 1000 mg subcutaneously once weekly for up to 12 weeks
  • Drug: Efgartigimod
    efgartigimod 1000 mg subcutaneous injection given once weekly
    Other names:
    • efgartigimod alfa and hyaluronidase-qvfc

Recruiting Locations

Stanford University
Palo Alto 5380748, California 5332921 94304-2210
Contact:
Travis Deal
650-723-7416
tdeal1@stanford.edu

More Details

Status
Recruiting
Sponsor
Stanford University

Study Contact

Travis Deal
650-723-7416
tdeal1@stanford.edu

Notice

Study information shown on this site is derived from ClinicalTrials.gov (a public registry operated by the National Institutes of Health). The listing of studies provided is not certain to be all studies for which you might be eligible. Furthermore, study eligibility requirements can be difficult to understand and may change over time, so it is wise to speak with your medical care provider and individual research study teams when making decisions related to participation.