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Recruiting Phase 2, Phase 3 NCT07204275

NCT07204275 Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN)

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Clinical Trial Summary
NCT ID NCT07204275
Status Recruiting
Phase Phase 2, Phase 3
Sponsor Vertex Pharmaceuticals Incorporated
Condition Primary Membranous Nephropathy
Study Type INTERVENTIONAL
Enrollment 176 participants
Start Date 2025-09-30
Primary Completion 2028-12-29

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age 75 Years
Study Type INTERVENTIONAL
Interventions
PovetaciceptTacrolimus

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

In Phase 2, researchers evaluate early signs of effectiveness. You may be randomized to receive the active treatment or a comparator. Monitoring continues closely.

This trial targets 176 participants in total. It began in 2025-09-30 with a primary completion date of 2028-12-29.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The purpose of this study is to evaluate the efficacy, safety, and tolerability of povetacicept in participants with primary membranous nephropathy (pMN).

Eligibility Criteria

Key Inclusion Criteria: • Diagnosed with pMN with confirmatory historical biopsy. If no historical biopsy was performed that confirmed pMN, a biopsy can be performed during Screening to confirm eligibility Key Exclusion Criteria: • Hypersensitivity to investigational medicinal product or to any of its excipients Other protocol defined Inclusion/Exclusion criteria will apply

Contact & Investigator

Central Contact

Medical Information

✉ medicalinfo@vrtx.com

📞 001-617-341-6777

Frequently Asked Questions

Who can join the NCT07204275 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, up to 75 Years, studying Primary Membranous Nephropathy. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

What phase is the NCT07204275 trial and what does that mean for participants?

Phase 2 trials evaluate whether the treatment shows signs of effectiveness while continuing to monitor safety. More participants are enrolled than in Phase 1 to help refine the treatment protocol.

Is NCT07204275 currently recruiting?

Yes, NCT07204275 is actively recruiting participants. Contact the research team at medicalinfo@vrtx.com for enrollment information.

Where is the NCT07204275 trial being conducted?

This trial is being conducted at Montgomery, United States, Surprise, United States, Los Angeles, United States, Tarzana, United States and 11 additional locations.

Who is sponsoring the NCT07204275 clinical trial?

NCT07204275 is sponsored by Vertex Pharmaceuticals Incorporated. The trial plans to enroll 176 participants.

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ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: July 2026  ·  Data Methodology