study to investigate the safety and efficacy properties of PF-00547659 in patients with active ulcerative colitis
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Enrollment
80
PF-00547659, single iv dose
PF-00547659, single iv dose
PF-00547659, multiple dose
Pfizer Investigational Site
Brussels, Belgium
Pfizer Investigational Site
Brussels, Belgium
Safety and toleration
Time frame: up to 12 weeks
Endoscopic score changes as calculated using section 3 of the Mayo Score
Time frame: up to 12 weeks
Disease activity score changes as calculated using the Mayo Score
Time frame: up to 12 weeks
Plasma concentrations of PF-00547659
Time frame: up to 12 weeks
Fecal concentrations of calprotectin
Time frame: up to 12 weeks
Plasma concentrations of CRP
Time frame: up to 12 weeks
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.
PF-00547659, single iv dose
PF-00547659, multiple dose
PF-00547659, single dose
PF-00547659, single dose
PF-00547659, single dose
PF-00547659, single dose
PF-00547659, multiple dose
PF-00547659, multiple dose
PF-00547659, multiple dose
PF-00547659, multiple dose
PF-00547659, multiple dose
PF-00547659, multiple dose
Pfizer Investigational Site
Leuven, Belgium
Pfizer Investigational Site
Brno, Czechia
Pfizer Investigational Site
Prague, Czechia
Pfizer Investigational Site
Prague, Czechia
Pfizer Investigational Site
Aarhus C, Denmark
Pfizer Investigational Site
Berlin, Germany
Pfizer Investigational Site
Kiel, Germany
Pfizer Investigational Site
Münster, Germany
...and 8 more locations