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A Study to Examine the Efficacy and Safety of Zanubrutinib Given to Adults With Primary Membranous Nephropathy
NCT05707377 · View on ClinicalTrials.gov ↗
Study Summary
The primary objectives of this study are: In Part 1 to evaluate the efficacy of zanubrutinib as measured by proteinuria reduction, and in Part 2 to evaluate the efficacy of zanubrutinib compared with tacrolimus as measured by complete remission rate, in participants with primary membranous nephropathy (PMN) who are on optimal supportive care.
Conditions Studied
Interventions
- DRUG Zanubrutinib
- DRUG Tacrolimus
Study Locations (20)
Fujian
- Fujian Medical University Union Hospital — Fuzhou
- The First Affiliated Hospital of Fujian Medical University — Fuzhou
- The First Affiliated Hospital of Xiamen University — Xiamen
Guangdong
- Guangdong Provincial Peoples Hospital — Guangzhou
- The First Affiliated Hospital, Sun Yat Sen University — Guangzhou
- Peking University Shenzhen Hospital — Shenzhen
California
- Amicis Research Center — Northridge
- Stanford University — Palo Alto
Other
- Instituto Pro Renal Brasil — Curitiba
- Hcfmusp Hospital Das Clinicas Da Faculdade de Medicina Da Universidade de Sao Paulo — São Paulo
Beijing Municipality
- Beijing An Zhen Hospital, Capital Medical University — Beijing
- Peking University First Hospital — Beijing
Minnesota
- Intermed Consultants — Minneapolis
Nevada
- Kidney Specialist of Southern Nevada (Ksosn) — Las Vegas
Ohio
- University of Cincinnati College of Medicine — Cincinnati
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 178 participants |
| Start Date | 2023-04-17 |
| Est. Completion | 2027-10 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT05707377
The ClinicalTrials.gov registry entry for NCT05707377 describes a study currently listed as active not recruiting. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 178 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is BeOne Medicines, which has 138 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Primary Membranous Nephropathy appearing as the primary indexed condition, and to 2 interventions — of which Zanubrutinib is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT05707377 reports 20 study locations spanning 13 distinct geographic areas — top geographies include Fujian, Guangdong, California. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT05707377 about?
NCT05707377 is a clinical study titled "A Study to Examine the Efficacy and Safety of Zanubrutinib Given to Adults With Primary Membranous Nephropathy". The primary objectives of this study are: In Part 1 to evaluate the efficacy of zanubrutinib as measured by proteinuria reduction, and in Part 2 to evaluate the efficacy of zanubrutinib compared with tacrolimus as measured by complete remission rate, in participants with primary membranous nephropat...
What is the current status of trial NCT05707377?
This trial is currently active not recruiting. It is a Phase 2 study. The enrollment target is 178 participants. The study started on 2023-04-17. Estimated completion is 2027-10.
What conditions does trial NCT05707377 study?
This clinical trial studies the following conditions: Primary Membranous Nephropathy. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT05707377?
The interventions under investigation include: Zanubrutinib (DRUG), Tacrolimus (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT05707377?
This trial is sponsored by BeOne Medicines, which has 138 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT05707377 being conducted?
This trial has 20 study locations across California, Minnesota, Nevada, Ohio, South Carolina. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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