Study to Evaluate the Effect of Bimosiamose on Ozone Induced Sputum Neutrophilia

NCT00962481 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 18

Last updated 2010-01-06

No results posted yet for this study

Summary

The purpose of this study is to evaluate the safety, tolerability and efficacy of repeated inhalative doses of Bimosiamose on ozone induced sputum neutrophilia in healthy subjects.

Conditions

  • Chronic Obstructive Pulmonary Disease (COPD)

Interventions

DRUG

Bimosiamose

DRUG

Placebo

Sponsors & Collaborators

  • Revotar Biopharmaceuticals AG

    lead INDUSTRY

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Model
CROSSOVER

Eligibility

Min Age
18 Years
Max Age
65 Years
Sex
ALL
Healthy Volunteers
Yes

Timeline & Regulatory

Countries

  • Germany

Study Locations

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Entities

Drugs

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 NCT00962481 on ClinicalTrials.gov