A Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients With ITP

PHASE2CompletedINTERVENTIONAL
Enrollment

38

Participants

Timeline

Start Date

March 13, 2017

Primary Completion Date

April 9, 2019

Study Completion Date

April 9, 2019

Conditions
Primary Immune Thrombocytopenia
Interventions
DRUG

ARGX-113

ARGX-113 (Dose A or Dose B) or matching placebo will be administered IV weekly

OTHER

Placebo

ARGX-113 (Dose A or Dose B) or matching placebo will be administered IV weekly

Trial Locations (30)

Unknown

Vienna, Vienna

Wien, Vienna

Leuven, Leuven

Mont-Godinne, Namur

Brno, Brno

Praha, Prague

Bordeaux, Bordeaux

Grenoble, Grenoble

Paris, Paris

Berlin, Berlin

Hanover, Hanover

Tubingen, Tübingen

Budapest, Budapest

Debrecen, Debrecen

Gyula, Gyula

Kaposvar, Kaposvár

Nyiregyhaza, Nyíregyháza

Pecs, Pécs

Lublin, Lublin

Opole, Opole

Wroclaw, Wroclaw

A Coruna, A Coruña

Barcelona, Barcelona

Madrid, Madrid

Valencia, Valencia

Dnipro, Dnipro

Ivano-Frankivsk, Ivano-Frankivsk

Nikolaev, Mykolayiv

Uzhgorod, Uzhhorod

London, London

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Quintiles, Inc.

INDUSTRY

lead

argenx

INDUSTRY

NCT03102593 - A Study to Evaluate the Safety, Efficacy, and Pharmacokinetics of ARGX-113 in Patients With ITP | Biotech Hunter | Biotech Hunter