A Study To Investigate The Safety And Efficacy Properties Of PF-00547659 In Patients With Active Ulcerative Colitis

NCT00928681 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 80

Last updated 2009-06-26

No results posted yet for this study

Summary

study to investigate the safety and efficacy properties of PF-00547659 in patients with active ulcerative colitis

Conditions

  • Colitis, Ulcerative

Interventions

BIOLOGICAL

Single dose-group A

PF-00547659, single iv dose

BIOLOGICAL

Single dose-group A

PF-00547659, single iv dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Single dose-group A

PF-00547659, single iv dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Single dose-group A

PF-00547659, single dose

BIOLOGICAL

Single dose-group A

PF-00547659, single dose

BIOLOGICAL

Single dose-group A

PF-00547659, single dose

BIOLOGICAL

Single dose-group A

PF-00547659, single dose

BIOLOGICAL

Multiple dose-Group B

PF-00547659, multiple dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Multiple dose- Group B

PF-00547659, multiple dose

BIOLOGICAL

Multiple dose-Group B

PF-00547659, multiple dose

Sponsors & Collaborators

Principal Investigators

  • Pfizer CT.gov Call Center · Pfizer

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
70 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2005-09-30
Primary Completion
2008-04-30
Completion
2008-10-31

Countries

  • Belgium
  • Czechia
  • Denmark
  • Germany
  • Norway
  • Slovakia
  • Spain

Study Locations

More Related Trials

Entities

Companies

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT00928681 on ClinicalTrials.gov