Povetacicept for Primary Membranous Nephropathy
This study is looking at how well and how safely povetacicept works for people with primary membranous nephropathy (pMN), a kidney disease. Researchers will compare povetacicept, given as a shot under the skin, with tacrolimus, taken as capsules by mouth. You might be able to join if you are between 18 and 75 years old and have a confirmed diagnosis of pMN. The main goal is to see how many participants achieve a complete clinical remission (CR1) after 104 weeks. The study is currently recruiting about 176 participants, but its status is unclear.
- Study design
- This interventional study plans to enroll 176 participants. It is evaluating two different treatments: povetacicept and tacrolimus.
- What's involved
- Not specified in the trial record.
- Compensation
- Not stated in the trial record.
- Follow-up
- The primary endpoint is measured at Week 104, suggesting participants will be followed for at least this duration.
AI-generated from the public study record. Only the study team can confirm whether you're eligible — confirm details with them before making decisions.
Evaluation of Efficacy, Safety, and Tolerability of Povetacicept in Participants With Primary Membranous Nephropathy (pMN)
At a glance
Conditions
Where it's being run
111 sites across 29 statesWho to contact
Opens a ready-to-send draft in your own email app — review before sending.
What this trial measures
- Proportion of Participants with Complete Clinical Remission Definition 1 (CR1)At Week 104