Ganitumab in locally advanced unresectable adenocarcinoma of the pancreas
Study Details
This study is a phase 2, multicenter, randomized, double-blind, active placebo-controlled trial of AMG 479 or placebo in combination with gemcitabine as first-line therapy for locally advanced unresectable adenocarinoma of the pancreas. Approximately 150 subjects will be randomized in a 1:1 ratio to AMG 479 and gemcitabine, or gemcitabine and placebo. Randomization will be stratified by ECOG (0 or 1).
Gemcitabine will be given on days 1, 8, and 15, followed by AMG 479 on days 1 and 15 of every 28 day cycle. Treatment will continue until radiographic disease progression, unacceptable toxicity, withdrawal of consent, or start of a new anti-cancer therapy.
Protocol Summary
The primary endpoint is progression-free survival (PFS) as defined as the time from randomization to progression (per RECIST v1.1) or death.
Timeframe: Approximately 23 months
Progression-free survival and overall survival rates at 3, 6, 9, 12, 18, and 24 months
Timeframe: Approximately 23 months
Objective response rate (complete or partial response) per RECIST v1.1
Timeframe: Approximately 23 months
Overall survival
Timeframe: Approximately 23 months