94
Participants
Start Date
November 30, 2013
Primary Completion Date
April 19, 2019
Study Completion Date
April 19, 2019
TroVax®
"Pre-amendment 10:~Patients will be randomised to receive either TroVax® 1 x 10↑9 TCID50/mL in 1mL (experimental arm) or matched placebo (control arm) on a 1:1 basis. A single dose will be given by intramuscular injection during the following weeks: 2, 4, 7, 10, 13, 19, 25, 31, 37, 43 and 49. No further treatment will be given beyond week 49.Treatment will be stopped early if confirmed progression or unacceptable toxicity.~Post-amendment 10:~Patients will be registered to receive TroVax 1 x 10↑9 TCID50/mL in 1mL only. A single dose will be given by intramuscular injection during the following weeks: 2, 4, 7, 10, 13, 19 and 25. No further treatment will be given beyond week 25.Treatment will be stopped early if confirmed progression or unacceptable toxicity."
Placebo
"Pre-amendment 10:~Matched placebo will be administered as above.~Post-amendment 10:~TRI-70 onwards received TroVax only."
Leeds Teaching Hospitals NHS Trust, Leeds
The Clatterbridge Cancer Centre NHS Foundation Trust, Bebington
Brighton and Sussex NHS Foundation Trust, Brighton
University Hospitals of Bristol NHS Foundation Trust, Bristol
Velindre NHS Trust, Cardiff
Beatson West of Scotland Cancer Centre, Glasgow
Royal Surrey County Hospital NHS Foundation Trust, Guildford
University College London Hospitals NHS Foundation Trust, London
The Christie NHS Foundation Trust, Manchester
Nottingham University Hospitals NHS Trust, Nottingham
Oxford University Hospitals NHS Trust, Oxford
Plymouth Hospitals NHS Trust, Plymouth
Collaborators (2)
Oxford BioMedica
INDUSTRY
Cancer Research UK
OTHER
University College, London
OTHER