A Phase 2 Study of Budoprutug in Subjects With Primary Membranous Nephropathy

Trial statusRecruiting
Trial phasePhase 2
Trial typeInterventional
Biological sexAll
Age18-75
SponsorClimb Bio, Inc.

About this trial

To evaluate the safety and tolerability of three dose regimens of budoprutug in subjects with PMN

Eligibility criteria

Qualifiers

Confirmed diagnosis of PMN with positive anti-PLA2R antibodies

CD19+ B cell count ≥40 cells/μL

UPCR ≥2.0 g/g

eGFR ≥35 mL/min/1.73 m²

Disqualifiers

Secondary Membranous Nephropathy

Rapidly progressive glomerulonephritis or other glomerulopathies

Prior B cell-depleting therapy within 24 weeks

Recent use of immunosuppressants

Trial design

Treatments tested in this trial

  • budoprutug

Treatment groups

45 Participants
are divided into 3 treatment groups

Sponsors and collaborators