Trial Condition(s):

Dermatitis, Atopic

Study to compare the efficacy and safety of Advantan ointment once daily with Protopic 0.03% ointment twice daily in children and adolescents with atopic dermatitis

Bayer Identifier:

Trial_308962

ClinicalTrials.gov Identifier:

Not Available

EudraCT Number:

Not Available

EU CT Number:

Not Available

Study Completed

Trial Purpose

Please see attached Study Results Summary below.

Inclusion Criteria

No Inclusion Criteria Available

Exclusion Criteria

No Exclusion Criteria Available

Trial Summary

Enrollment Goal

265

Trial Dates

March2005

August2005

Phase

Could I receive a placebo?

Products

Advantan (Methylprednisolone Aceponate, BAY86-4862)

Accepts Healthy Volunteers

N/A

Where to Participate

Locations

Locations

Dermatitis, Atopic

Bayer Identifier:

ClinicalTrials.gov Identifier:

EudraCT Number:

EU CT Number:

Trial Purpose

Key Participation Requirements

sex

age

2 Years

15 Years

Inclusion Criteria

Exclusion Criteria

Inclusion Criteria

Exclusion Criteria

Trial Summary

Enrollment Goal

Trial Dates

Phase

Could I receive a placebo?

Products

Accepts Healthy Volunteers

Where to Participate

For details, please refer to trial results

Additional Information