Open-Label Phase II Study to Evaluate the Efficacy and Safety of IdeS in Anti-GBM Disease

PHASE2CompletedINTERVENTIONAL
Enrollment

15

Participants

Timeline

Start Date

June 16, 2017

Primary Completion Date

July 24, 2020

Study Completion Date

July 24, 2020

Conditions
Anti-Glomerular Basement Membrane Antibody Disease
Interventions
BIOLOGICAL

Imlifidase

One dose of 0.25 mg/kg body weight imlifidase on study day 1

Trial Locations (10)

2100

Department of Department of Nephrology, Rigshospitalet, Copenhagen, Copenhagen

6020

Department of Internal Medicine IV (Nephrology and Hypertension), Innsbruck

31059

Department of Nephrology and Organ Transplant, CHU Rangueil, Toulouse

59000

Centre Hospitalier Régional Universitaire de Lille, Nephrology Service, Lille

75018

Nephrology Service CHU Bichat, Paris

75020

PH USI UNTR, service du Pr Rondeau, Hôpital Tenon, Paris

75185

Department of Nephrology, Uppsala University Hospital, Uppsala

121 08

Department of Department of nephrology, First Faculty of Medicine and General Teaching Hospital and Charles University in Prague, Czech Republic,, Prague

Unknown

Department of Nephrology, Hemodialysis, Apheresis, and Transplantation, CHUGA (centre hospitalier universitaire Grenoble-Alpes), Grenoble

141 86

Karolinska University Hospital Huddinge, Stockholm

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Hansa Biopharma AB

INDUSTRY

lead

Mårten Segelmark

OTHER_GOV

NCT03157037 - Open-Label Phase II Study to Evaluate the Efficacy and Safety of IdeS in Anti-GBM Disease | Biotech Hunter | Biotech Hunter