Comparison of Efficacy of Indacaterol Versus Placebo Over 12 Weeks

NCT01068600 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 318

Last updated 2011-08-19

Study results available
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Summary

This 12-week study evaluated the efficacy and safety of indacaterol versus placebo.

Conditions

Interventions

DRUG

Indacaterol

Once daily via single-dose dry powder inhaler (SDDPI)

DRUG

Placebo to indacaterol

Once daily via SDDPI

Sponsors & Collaborators

Principal Investigators

  • Novartis Pharmaceuticals · Novartis Pharmaceuticals

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
PARALLEL

Eligibility

Min Age
40 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2010-01-31
Primary Completion
2010-06-30

Countries

  • United States

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 NCT01068600 on ClinicalTrials.gov