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Atacicept in Subjects With IgA Nephropathy

About

Brief Summary

A Phase 3 Study with Atacicept in Subjects With IgA Nephropathy (ORIGIN 3)

Primary Purpose
Treatment
Study Type
Interventional
Phase
Phase 2/Phase 3

Eligibility

Gender
All
Healthy Volunteers
No
Minimum Age
18 Years
Maximum Age
N/A

Key Inclusion Criteria:

  • Must have the ability to understand and sign a written informed consent form
  • Male or female of ≥18 years of age
  • Total urine protein excretion ≥1.0 g per 24-hour or urine protein to creatinine ratio (UPCR) ≥1.0 mg/mg based on a 24-hour urine sample during the Screening Period
  • Diagnosis of IgAN as demonstrated by renal biopsy conducted within 10 years
  • eGFR ≥ 30 mL/min/1.73 m2, as per the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) equation.
  • On a stable prescribed regimen of RAASi for at least 12 weeks that is at the maximum labeled or tolerated dose at Screening
  • Systolic blood pressure ≤150 mmHg and diastolic blood pressure ≤90 mmHg

Key Exclusion Criteria:

  • IgAN secondary to another condition (e.g., liver cirrhosis), or other causes of mesangial IgA deposition including IgA vasculitis (i.e., Henoch-Schonlein purpura), systemic lupus erythematosus (SLE), dermatitis herpetiformis, ankylosing spondylitis
  • Total urine protein excretion ≥ 5g per 24-hour or urine protein to creatinine ratio (UPCR) ≥ 5 mg/mg based on a 24-hour urine sample during the Screening Period
  • Evidence of rapidly progressive glomerulonephritis (loss of ≥ 50% of eGFR within 3 months of screening)
  • Evidence of nephrotic syndrome within 6 months of screening (serum albumin <30g/L in association with UPCR >3.5 mg/mg
  • Renal or other organ transplantation prior to, or expected during the study
  • Concomitant chronic renal disease in addition to IgAN
  • Uncontrolled diabetes, defined as hemoglobin-A1c (HbA1c) >7.5% at screening
  • History of tuberculosis (TB), untreated latent TB infection (LTBI), or evidence of active TB determined by a positive Quantiferon test
  • Participation in the Phase 2b (Parts A and B) study or any previous treatment with atacicept

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Study Stats
Protocol No.
23-5139
Category
Genitourinary Disorders
Contact
Jessica Gomez
Location
  • UCLA Westwood
For Providers
NCT No.
NCT04716231
For detailed technical eligibility, visit ClinicalTrials.gov.