28 Day Repeat Dose in Cystic Fibrosis Patients

NCT00903201 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 146

Last updated 2017-11-17

Study results available
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Summary

The purpose of this study is to determine whether the safety, tolerability and pharmacodynamics of SB656933 in patients that have cystic fibrosis

Conditions

Interventions

DRUG

SB656933

20 mg

DRUG

SB656933

50mg

DRUG

Placebo

placebo

Sponsors & Collaborators

Principal Investigators

  • GSK Clinical Trials · GlaxoSmithKline

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2009-09-28
Primary Completion
2010-12-29
Completion
2010-12-29

Countries

  • United States
  • Canada
  • France
  • Germany
  • Israel

Study Locations

More Related Trials

Entities

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 NCT00903201 on ClinicalTrials.gov