deltatrials
Recruiting PHASE3 INTERVENTIONAL 3-arm NCT05914155

Clinical Study of Rituximab for the Treatment for Idiopathic Membranous Nephropathy with Nephrotic Syndrome (PRIME)

The Multi-center, Randomized, Double-blind, Placebo-controlled Study to Evaluate the Efficacy and Safety of Rituximab (Genetical Recombination) for the Treatment for Idiopathic Membranous Nephropathy with Nephrotic Syndrome (PRIME Study)

Sponsor: Shoichi Maruyama MD PhD

Updated 6 times since 2023 Last updated: Feb 9, 2025 Started: Jun 24, 2023 Primary completion: Dec 31, 2027 Completion: Dec 31, 2027
This information is for research purposes only and is not medical advice. Consult a healthcare provider before making any medical decision.

This PHASE3 trial investigates Glomerulonephritis, Membranous and Nephrotic Syndrome,Idiopathic and is currently actively recruiting participants. Shoichi Maruyama MD PhD leads this study, which shows 6 recorded versions since 2023 — indicating limited longitudinal coverage. The change history captured here reflects the iterative nature of clinical trial conduct.

Status Flow

~Jul 2023 – ~Aug 2023 · 31 days · monthly snapshot~Aug 2023 – ~Jul 2024 · 11 months · monthly snapshotRecruiting~Jul 2024 – ~Sep 2024 · 2 months · monthly snapshot~Sep 2024 – ~Nov 2024 · 2 months · monthly snapshot~Nov 2024 – ~Mar 2025 · 4 months · monthly snapshotRecruiting~Mar 2025 – present · 17 months · monthly snapshotRecruiting

Change History

6 versions recorded
  1. Mar 2025 — Present [monthly]

    Recruiting PHASE3

  2. Nov 2024 — Mar 2025 [monthly]

    Recruiting PHASE3

  3. Sep 2024 — Nov 2024 [monthly]

    Recruiting PHASE3

  4. Jul 2024 — Sep 2024 [monthly]

    Recruiting PHASE3

  5. Aug 2023 — Jul 2024 [monthly]

    Recruiting PHASE3

    Status: Not Yet RecruitingRecruiting

Show 1 earlier version
  1. Jul 2023 — Aug 2023 [monthly]

    Not Yet Recruiting PHASE3

    First recorded

Jun 2023

Trial started

Per CT.gov start date — pre-dates our first snapshot

Eligibility Summary

No eligibility information available.

Contact Information

Sponsor contact:
  • Shoichi Maruyama MD PhD
Data source: Nagoya University

For direct contact, visit the study record on ClinicalTrials.gov .