Experimental drug for rare inflammatory disease shows early promise but trial cut short
NCT ID NCT04918147
First seen Jun 27, 2026 ยท Last updated Jun 27, 2026
Summary
This study tested elotuzumab, a drug used for multiple myeloma, in people with active IgG4-related disease (IgG4-RD), a rare condition causing inflammation and organ damage. The trial was small (only 8 participants) and was terminated early, so it is unclear if the drug is safe or effective. Participants received either elotuzumab plus prednisone or a placebo plus prednisone, and the main goal was to check for side effects.
What this could mean
Our plain-language read of the trial. This is informational only โ not medical advice or a prediction.
- Active substance
- elotuzumab (a monoclonal antibody)
- What this could lead to
- If it works, this could point toward a new treatment option for IgG4-related disease, reducing reliance on steroids.
- What could go wrong
- This trial was terminated early with only 8 participants enrolled, so results are very limited. It is too early to know if elotuzumab is safe or effective for this condition.
This is an AI summary of the original study and may miss details. Read our disclaimer.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Emory Healthcare
Atlanta, Georgia, 30322, United States
-
Massachusetts General Hospital
Boston, Massachusetts, 02114, United States
-
Mayo Clinic: Pulmonary and Critical Care Medicine
Rochester, Minnesota, 55905, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New drug aims to stop IgG4 disease relapses without Long-Term steroids
- Experimental CAR-T injection aims to tame autoimmune diseases
- Scientists investigate immune cell role in rare IgG4 disease
- Old drug, new hope: could filgotinib tame rare immune diseases?
- New scan could shine a light on hidden inflammation
- New drug shows promise for rare inflammatory disease