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NCT07902817

A Phase 3 Blinded Study of JADE101 in Participants With Immunoglobulin A Nephropathy

StatusRecruiting
PhasePhase 3
Primary completion (estimated)
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Record History

All 2 versions: 2 with changes below.

  1. Notable Recruitment opened
    • Trial sites expanded: 0 → 4 locations
  2. Study First Submitted
  • Notable: the plan changed

Endpoints

Primary

To evaluate the effect of JADE101 on Urine Protein Creatinine Ratio (UPCR) in participants with IgA nephropathy
Timeframe: Week 52

Secondary (1)

To evaluate the effect of JADE101 on Estimated Glomerular Filtration Rate (eGFR) in participants with IgA nephropathy

Arms and interventions

JADE101 Q8WExperimental

Subcutaneous (SC) injection of JADE101 with Q8W maintenance dosing

JADE101 Q12WExperimental

Subcutaneous (SC) injection of JADE101 with Q12W maintenance dosing

PlaceboPlacebo comparator

Subcutaneous (SC) injection of placebo during the placebo-controlled treatment period

Drugs: JADE101, Placebo

Sites

4 sites in 1 country