140
Participants
Start Date
December 31, 2010
Primary Completion Date
January 31, 2012
Study Completion Date
March 31, 2012
FX005
Single Ascending Dose (SAD) Phase Cohorts: 1, 10 or 45 mg intra-articular injection; Proof of Concept Phase: Maximum, well-tolerated dose intra-articular injection (determined during SAD Phase)
Placebo 1 (Carrier)
Single intra-articular injection
Placebo 2 (Diluent)
Single intra-articular injection
Graz
Vienna
Penticton
Newmarket
Toronto
Windsor
Sainte-Foy
Santiago de Compostela
Santander
A Coruña
Barcelona
Seville
Southampton
Lead Sponsor
Pacira Pharmaceuticals, Inc
INDUSTRY