28 Day Repeat Dose in Cystic Fibrosis Patients
NCT00903201 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 146
Last updated 2017-11-17
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
Sponsors & Collaborators
- lead INDUSTRY
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
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