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WAL 801 CL Dry Syrup in Paediatric Atopic Dermatitis Patients

NCT02182557 · Status: COMPLETED · Phase: PHASE3 · Type: INTERVENTIONAL · Enrollment: 162

Last updated 2014-07-14

No results posted yet for this study

Summary

Study to investigate the safety and efficacy of WAL 801 CL Dry Syrup on pruritus associated with paediatric atopic dermatitis in comparison with that of Ketotifen Fumarate Dry Syrup and to confirm the appropriateness of dosage of WAL801 Dry Syrup.

Conditions

  • Dermatitis, Atopic

Interventions

DRUG

WAL 801 CL Dry Syrup

DRUG

Ketotifen Fumarate Dry Syrup

DRUG

WAL 801 CL Dry Syrup placebo

DRUG

Ketotifen Fumarate Dry Syrup placebo

Sponsors & Collaborators

Study Design

Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
DOUBLE
Model
PARALLEL

Eligibility

Max Age
15 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2001-06-30
Primary Completion
2002-01-31

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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 NCT02182557 on ClinicalTrials.gov