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

RecruitingPhase 2

A Phase 2, Open-Label Study to Evaluate the Safety and Efficacy of Budoprutug (TNT119) in Subjects With Primary Membranous Nephropathy (PMN)

Who can join

Ages 18 to 75 · All sexes

Full eligibility criteria
Inclusion Criteria:

* 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
* Stable RAAS inhibitor therapy
* Blood pressure \<150/90 mmHg at baseline
* Adequate hematologic, hepatic, and renal function
* Willing to use effective contraception (both sexes)
* Other inclusion criteria may apply

Exclusion Criteria:

* Secondary Membranous Nephropathy
* Rapidly progressive glomerulonephritis or other glomerulopathies
* Prior B cell-depleting therapy within 24 weeks
* Recent use of immunosuppressants
* Active or high-risk infections
* History of malignancy
* Pregnancy or breastfeeding
* Recent major surgery or hospitalization
* Other exclusion criteria may apply

About the study

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

What is being tested

Sponsor: Climb Bio, Inc. · Participants: 45 · Started: Aug 25, 2025

Contact the study team

Official record on ClinicalTrials.gov — NCT07096843

Locations in the U.S.

ColoradoClimb Bio Investigative Site #110, Denver
FloridaClimb Bio Investigative Site #105, Orlando
GeorgiaClimb Bio Investigative Site #108, Atlanta
IndianaClimb Bio Investigative Site #106, Indianapolis
MassachusettsClimb Bio Investigative Site #111, Boston (Not yet recruiting)
New YorkClimb Bio Investigative Site #101, Clifton Park
TexasClimb Bio Investigative Site #104, Sherman

From ClinicalTrials.gov, data retrieved Sep 30, 2026. Each study sets its own eligibility; the study team decides who can join.