53
Participants
Start Date
January 21, 2019
Primary Completion Date
March 29, 2024
Study Completion Date
April 30, 2026
rAd-IFN
Adenovirus-Delivered Interferon Alpha-2b
Celecoxib Oral Product
400 mg twice daily
Gemcitabine
1250 mg/m2 administered intravenously on Days 1 and 8 of a 21-day cycle and continued every 3 weeks until disease progression/ early termination
Chris O'Brien Lifehouse, Camperdown
Monash Medical Centre, Clayton
CHU de Caen - Hopital Cote de Nacre, Caen
University of Pennsylvania Abramson Cancer Center, Philadelphia
Marlene & Stewart Greenbaum Comprehensive Cancer Center, Baltimore
University of Maryland Medical Center, Baltimore
CHRU de Brest - Hopital Augustin Morvan, Brest
Institut Bergonie, Bordeaux
H. Lee Moffitt Cancer Center & Research Institute, Tampa
CHU de Nantes - Hôpital Nord Laennec, Saint-Herblain
Azienda Ospedaliero Universitaria Senese, Cancer Immunotherapy, Siena
Masonic Cancer Center - University of Minnesota, Minneapolis
CHRU de Lille, Lille
Evangelisches Krankenhaus Hamm, Hamm
Institut Curie - Oncologie Medicale, Paris
University of California, Los Angeles (UCLA) - Medical Center, Los Angeles
Universitatsklinikum Regensburg, Regensburg
University of California, San Francisco (UCSF), San Francisco
Petrov National Medical Research Center of Oncology, Saint Petersburg
Volgograd Regional Clinical Oncology Dispensary, Volgograd
Institut Universitaire de Cardiologie et de Pneumologie De Quebec, Québec
Centre Hospitalier Lyon Sud, Pierre-Bénite
Med Polonia Sp. z o.o., Poznan
Centrum Onkologii Instytut im. Marii Sklodowskiej - Curie, Klinika Nowotworow Tkanek Miekkich, Kosci i Czerniakow, Warsaw
Derriford Hospital ; Derriford Hospital, Plymouth
Beatson, West of Scotland Cancer Centre, Glasgow
Royal Marsden Foundation Trust, Sutton
Guy's and St. Thomas' NHS Trust, London
Churchill Hospital, Oxford
University of Pennsylvania
OTHER
Ferring Ventures Limited
INDUSTRY