98
Participants
Start Date
March 26, 2019
Primary Completion Date
May 29, 2020
Study Completion Date
June 10, 2020
Fevipiprant 150 mg
Fevipiprant (QAW039) 150 mg once daily administered orally as tablet
Fevipiprant 450 mg
Fevipiprant (QAW039) 450 mg once daily administered orally as tablet
Placebo
Placebo once daily administered orally as tablet
Novartis Investigative Site, Brussels
Novartis Investigative Site, San Miguel de Tucumán
Novartis Investigative Site, Erpent
Novartis Investigative Site, Mendoza
Novartis Investigative Site, Rozzano
Novartis Investigative Site, Kladno
Novartis Investigative Site, Pisa
Novartis Investigative Site, Frankfurt
Novartis Investigative Site, Irvine
Novartis Investigative Site, CABA
Novartis Investigative Site, CABA
Novartis Investigative Site, CABA
Novartis Investigative Site, Florida
Novartis Investigative Site, Rosario
Novartis Investigative Site, Buenos Aires
Novartis Investigative Site, Ottawa
Novartis Investigative Site, Québec
Novartis Investigative Site, Olomouc
Novartis Investigative Site, Svitavy
Novartis Investigative Site, Dresden
Novartis Investigative Site, Roma
Novartis Investigative Site, Amsterdam
Novartis Investigative Site, Enschede
Novartis Investigative Site, Strzelce Opolskie
Novartis Investigative Site, Zawadzkie
Lead Sponsor
Novartis Pharmaceuticals
INDUSTRY