Phase 2 Vasculitis Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
You weigh at least 40 kg (about 88 pounds)
You are currently on a stable, prescribed treatment plan for your kidney condition, following local medical guidelines
Your blood pressure at your screening visit is not too high (top number no more than 160, bottom number no more than 90)
You have been diagnosed with one of these kidney conditions: IgA nephropathy (IgAN), IgA vasculitis with nephritis (IgAVN), primary membranous nephropathy (pMN), minimal change disease (MCD), focal segmental glomerulosclerosis (FSGS), or primary nephrotic syndrome
If you are an adult (18+) with IgAN: Your diagnosis has been confirmed by a kidney biopsy, your kidneys are functioning at a certain minimum level, and you have a measurable amount of protein in your urine
If you are a child (age 2–17) with IgAN or IgAVN: Your diagnosis has been confirmed by a kidney biopsy, you have been on a stable treatment for at least 8 weeks, your kidneys are functioning at a minimum level, and you have protein in your urine
If you are an adult with pMN: Your diagnosis has been confirmed by a kidney biopsy, you have a specific antibody in your blood (anti-PLA2R) above a certain level, you have protein in your urine, and you are considered unlikely to get better on your own
If you have nephrotic syndrome (MCD, FSGS, or childhood nephrotic syndrome): You are age 10 or older, your kidneys are functioning at a minimum level, you have protein in your urine, and you have a specific antibody called anti-nephrin in your blood
Who may not be able to join:
- Your kidney function has dropped by 50% or more in the 12 weeks before your screening visit
- You currently have an active viral or bacterial infection
- You have other health conditions or abnormal lab results that could interfere with safely taking part in the study (confirm with trial site)
- You have received a live vaccine in the 30 days before enrolling
- You have taken immune-suppressing medications in the 4 weeks before starting the study drug (with an exception for people on transplant anti-rejection medications)
- You have had an allergic reaction to atacicept (the study drug) or any of its ingredients in the past
- There are additional requirements specific to each disease group that may affect eligibility (confirm with trial site)
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Pam Winterberg, Vera Therapeutics
Phone: 650-770-0077
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
AE profile and results of routine clinical and laboratory tests; Percent reduction in urine protein to creatinine ratio (UPCR)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 28 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.