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Dose Response of Inhaled Tacrolimus in Patients With Moderate Persistent Asthma

NCT00189787 · Status: COMPLETED · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 370

Last updated 2008-04-17

No results posted yet for this study

Summary

This study will evaluate the efficacy and safety of tacrolimus in patients with asthma.

Conditions

  • Asthma, Bronchial
  • Bronchial Asthma

Interventions

DRUG

tacrolimus

Sponsors & Collaborators

  • Astellas Pharma Europe B.V.

    collaborator INDUSTRY

  • Astellas Pharma Inc

    lead INDUSTRY

Principal Investigators

  • R.G.M.vom Amsterdam, MD · Astellas Pharma Europe B.V.

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

Primary Completion
2005-08-31
Completion
2005-08-31

Countries

  • Bulgaria
  • Czechia
  • Germany
  • Hungary
  • Poland
  • Russia
  • Ukraine

Study Locations

More Related Trials

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 NCT00189787 on ClinicalTrials.gov