Researching Vonsetamig and Odronextamab for Lupus Nephritis

This study is looking into two experimental drugs, Vonsetamig and Odronextamab, for adults with Lupus Nephritis (LN). LN is a serious kidney disease caused by lupus. The main goal is to understand how safe these drugs are and what side effects they might cause over a long period. This is an 'umbrella study,' meaning it includes several smaller studies testing different drugs for LN at the same time. You might be able to join if you are 18 to 60 years old, have been diagnosed with Systemic Lupus Erythematosus (SLE) and LN, and your disease has not responded well to other treatments or has come back. The study is also looking at how much drug is in the blood and if your body makes antibodies against the drugs.

Study design
This is an interventional study planning to enroll 90 participants. It is a dose escalation study, meaning different doses of the drugs will be tested.
What's involved
Not specified in the trial record.
Compensation
Not stated in the trial record.
Follow-up
Participants will be followed for treatment-emergent adverse events and their severity through week 76.

AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.

NCT06975787

Dose Escalation Study With Bispecific Antibodies in Adult Participants With Lupus Nephritis

Recruiting
PHASE1Ages 18–60InterventionalTreatment
Regeneron Pharmaceuticals
~90 participants
Updated 2026-08-13 on ClinicalTrials.gov
What's tested:VonsetamigOdronextamab

At a glance

Recruiting sites
18 of 18 listed sites are recruiting right now
RecruitingSuspended, closed, or not yet open
What they're measuring
Occurrence of Dose Limiting Toxicities (DLT)
Measured over Up to 56 days
+2 more outcomes measured
Lupus Nephritis (LN)
18 sites across 11 states
Taiwan4
South Korea3
Spain3
Minnesota1
Texas1
New Aquitaine1
Bavaria1
Germany1
  • Clinical Trial Management · STUDY_DIRECTOR · Regeneron Pharmaceuticals

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  • Occurrence of Dose Limiting Toxicities (DLT)Up to 56 days
  • Occurrence of Treatment Emergent Adverse Events (TEAEs)Through week 76
  • Severity of TEAEsThrough week 76