144
Participants
Start Date
September 1, 2016
Primary Completion Date
November 8, 2017
Study Completion Date
August 23, 2019
Andecaliximab
800 mg administered via IV infusion
Nivolumab
3 mg/kg administered via IV infusion
Wahroonga
Albury
Leuven
Debrecen
Douglas
Hobart
La Louvière
Ghent
New York
Genova
Milan
Majadahonda
Brest
Fort Wayne
Meldola
Reims
Pisa
Chicago
St Louis
Los Angeles
San Francisco
Villejuif
Budapest
Brzozów
Poznan
Warsaw
Barcelona
Barcelona
Bristol
Edgbaston
London
London
Manchester
Sutton
Lead Sponsor
Gilead Sciences
INDUSTRY