A Study to Evaluate the Efficacy and Safety of VIB4920 in Participants With Sjögren's Syndrome

Completed · Phase 2 · Has a placebo group

Conditions studied: Sjögren's Syndrome

In brief

The purpose of the study is to evaluate the efficacy, safety, and tolerability of VIB4920 (formerly MEDI4920) in adult participants with Sjögren's Syndrome (SS).

Key facts

Study ID: NCT04129164
Run by: Amgen
People needed: 183
Starts: 2019-12-09
Expected to finish: 2023-03-10
Last updated by the study team: 2025-04-30

Who can join

Age: 18 and older, up to 75. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

Diagnosed with SS by meeting the 2016 American College of Rheumatology (ACR)/EULAR Classification Criteria.
Residual salivary gland function as defined by whole stimulated salivary flow > 0.1 mL/min (only for Population 2).
Have an ESSDAI score of >= 5 at screening; (not including the peripheral nervous system, central nervous system, and pulmonary domains) (only for Population 1).
Have an ESSPRI score of >= 5 at screening (only for Population 2).
Have an ESSDAI score of < 5 at screening (only for Population 2).
Positive for either anti-Ro autoantibodies or rheumatoid factor, or both at screening.
Male and female participants who agree to follow protocol defined contraceptive methods.
No active or untreated latent tuberculosis (TB).

You may not qualify if…

Medical history of confirmed deep venous thrombosis or arterial thromboembolism within 2 years of signing the informed consent form (ICF).
Risk factors for venous thromboembolism or arterial thrombosis, prothrombotic status.
Concomitant polymyositis or dermatomyositis or systemic sclerosis.
Active malignancy or history of malignancy, except in situ carcinoma of the cervix and cutaneous basal cell carcinoma.
Hepatitis B, hepatitis C, or human immunodeficiency virus infection.
More than one episode of herpes zoster and/or an opportunistic infection in the last 12 months.
Active viral, bacterial, or other infections or history of more than 2 infections requiring intravenous antibiotics within 12 months prior to signing the ICF.
Participants with corona virus disease 2019 (COVID-19) infection or who, in the judgment of the investigator, are at unacceptable risk of COVID-19 or its complications.
A documented positive severe acute respiratory syndrome-coronavirus-2 (SARS-CoV-2) test within 2 weeks prior to randomization.
Received live (attenuated) vaccine within the 4 weeks prior to ICF signature.
Treated with any biologic B-cell-depleting therapy within 12 months or other B-cell targeting therapy < 3 months before randomization.
Injectable corticosteroids (including intraarticular) or treatment with > 10 mg/day dose oral prednisone or equivalent within 6 weeks prior to randomization (only for Population 1).
Treated with systemic corticosteroids for indications other than SS, rheumatoid arthritis (RA), and systemic lupus erythematosus (SLE) for more than a total of 2 weeks within 24 weeks prior to screening visit (only for Population 1).
Received previous treatment with anti-CD40L compounds at any time before screening.
Pregnant or lactating or planning to get pregnant during the duration of the study.

Where it is running

Research site — Upland, California, United States
Research Site — Lawrenceville, Georgia, United States
Research Site — Kansas City, Kansas, United States
Research Site — Baltimore, Maryland, United States
Research Site — Wheaton, Maryland, United States
Research Site — Boston, Massachusetts, United States
Research Site — Charlotte, North Carolina, United States
Research Site — Durham, North Carolina, United States
Research Site — Salisbury, North Carolina, United States
Research Site — Wilmington, North Carolina, United States
Research site — Duncansville, Pennsylvania, United States
Research Site — Memphis, Tennessee, United States
Research site — Dallas, Texas, United States
Research Site — Houston, Texas, United States
Research Site — Houston, Texas, United States
Research Site — Ciudad Autonoma de Buenos Aires, Buenos Aires, Argentina
Research Site — Bordeaux, France
Research Site — Brest, France
Research Site — Grenoble, France
Research Site — Paris, France
Research Site — Strasbourg, France
Research Site — Budapest, Hungary
Research Site — Debrecen, Hungary
Research Site — Gyula, Hungary
Research Site — Fullerton, California, United States

Full record on ClinicalTrials.gov

Trial information comes from ClinicalTrials.gov and is refreshed daily. TrialsForMe does not provide medical care and does not run the studies it lists.