A Phase 2 Study of Budoprutug in Subjects With Primary Membranous Nephropathy
NCT07096843 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 45
Last updated 2026-04-30
Summary
To evaluate the safety and tolerability of three dose regimens of budoprutug in subjects with PMN
Conditions
Interventions
- DRUG
-
budoprutug
Single IV dose of study product on Day 1, Day 15, Day 169 and Day 183
Sponsors & Collaborators
-
Climb Bio, Inc.
lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SEQUENTIAL
Eligibility
- Min Age
- 18 Years
- Max Age
- 75 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2025-08-25
- Primary Completion
- 2027-10-31
- Completion
- 2027-10-31
- FDA Drug
- Yes
Countries
- United States
- Argentina
- Brazil
- Chile
- China
- Georgia
- Taiwan
- Ukraine
Study Locations
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