46
Participants
Start Date
January 15, 2015
Primary Completion Date
April 5, 2017
Study Completion Date
April 5, 2017
Rivaroxaban (Xarelto, BAY59-7939)
With age and body-weight adjusted twice daily dosing of rivaroxaban as Oral Suspension to achieve a similar exposure as that observed in adults treated with 20 mg rivaroxaban once daily, and no other anticoagulant
Vienna
Budapest
Bern
Parkville
Turin
Milan
Children's Healthcare of Atlanta, Atlanta
Pensacola
Gainesville
Padua
Valencia
Indianapolis
Chicago
Moscow
Saint Petersburg
Nizhny Novgorod
Ramat Gan
Jerusalem
São Paulo
São Paulo
Toronto
Setagaya City
Nijmegen
Gdansk
Olsztyn
Barcelona
Newcastle upon Tyne
Birmingham
Cardiff
Lead Sponsor
Janssen Research & Development, LLC
INDUSTRY
Bayer
INDUSTRY