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Terminated Phase 3 Interventional

A Study With Imlifidase in Anti-GBM Disease

ClinicalTrials.gov ID: NCT05679401

Public ClinicalTrials.gov record NCT05679401. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Jul 23, 2026, 11:33 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase 3 Open-label, Controlled, Randomised, Multi-centre Trial Comparing Imlifidase and Standard-of-care With Standard-of-care Alone in the Treatment of Severe Anti-GBM Antibody Disease (Goodpasture Disease)

Study identification

NCT ID
NCT05679401
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 3
Lead sponsor
Hansa Biopharma AB
Industry
Enrollment
50 participants

Conditions and interventions

Interventions

  • Imlifidase Drug
  • Plasma exchange (PLEX) Procedure
  • Cyclophosphamide (CYC) Drug
  • Glucocorticoids Drug

Drug · Procedure

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 21, 2022
Primary completion
Jun 22, 2025
Completion
Feb 1, 2026
Last update posted
Mar 3, 2026

2022 – 2026

United States locations

U.S. sites
6
U.S. states
6
U.S. cities
6
Facility City State ZIP Site status
UCLA Medical Center Plaza Los Angeles California 90024
John Hopkins Medical Institution Baltimore Maryland 21287
Brigham and Women's Hospital Boston Massachusetts 02115
University of Minnesota Health Clinical Research Unit Minneapolis Minnesota 55455
UNC Kidney Center/Division of Nephrology & Hypertension Chapel Hill North Carolina 27599-7155
The Ohio State University Wexner Medical Center Columbus Ohio 43201

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 42 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05679401, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Mar 3, 2026 · Synced Jul 23, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT05679401 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →