Phase 2 Vasculitis Trial, Recruiting NCT06983028 Sponsor: Vera Therapeutics, Inc. Condition: Vasculitis
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Phase 2 Vasculitis Trial, Recruiting

NCT06983028
Recruiting Phase 2

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 28 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

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

Status
Recruiting
Phase
Phase 2
Sponsor
Vera Therapeutics, Inc.
Registry
ClinicalTrials.gov
Start date
7 July 2025
Est. completion
1 November 2027

Where this trial is recruiting

🇺🇸 United States

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?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

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.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov