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Safety, Efficacy and Pharmacokinetic Study of Allegra in Pediatric Patients With Perennial Allergic Rhinitis (PAR)

Phase 2
Completed
Conditions
Rhinitis Perennial
Interventions
Drug: fexofenadine/Allegra (M016455)
Registration Number
NCT01244217
Lead Sponsor
Sanofi
Brief Summary

Primary Objective:

- To evaluate safety (4 weeks)

Secondary Objectives:

* To evaluate the long-term safety (12 weeks)

* To evaluate the efficacy

* To characterize the pharmacokinetic profile

Detailed Description

The study consists of four phases: up to 9-day screening phase, main 4-week treatment phase, up-to 8-week extension phase, and up-to 5-day post-treatment phase.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
100
Inclusion Criteria

Not provided

Exclusion Criteria

Not provided

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
Age 6 months - 2 yearsfexofenadine/Allegra (M016455)Patients between 6 months and 2 years old
Age 2 - 11 yearsfexofenadine/Allegra (M016455)Patients between 2 and 11 years (and under 10.5 kg)
Age 2 - 11 years (and over 10.5 kg)fexofenadine/Allegra (M016455)Patients between 2 and 11 years (and over 10.5 kg)
Primary Outcome Measures
NameTimeMethod
The number of clinically significant abnormalities for laboratory findings4 weeks
Number of patients with adverse events4 weeks
Secondary Outcome Measures
NameTimeMethod
Number of patients with adverse events12 weeks
Changes from baseline in nasal symptom scores on patient diary4 weeks
Pharmacokinetic parameters of fexofenadine at steady state; AUCweek 4 and 12
The number of clinically significant abnormalities for laboratory findings12 weeks
Changes from baseline in nasal symptom severity scores assessed by investigator or subinvestigatorweek 2 and 4

Trial Locations

Locations (15)

Sanofi-Aventis Investigational Site Number 392015

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Fukuoka-Shi, Japan

Sanofi-Aventis Investigational Site Number 392003

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Kawasaki-Shi, Japan

Sanofi-Aventis Investigational Site Number 392004

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Kawasaki-Shi, Japan

Sanofi-Aventis Investigational Site Number 392008

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Yokohama-Shi, Japan

Sanofi-Aventis Investigational Site Number 392013

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Seki-Shi, Japan

Sanofi-Aventis Investigational Site Number 392009

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Yokohama-Shi, Japan

Sanofi-Aventis Investigational Site Number 392001

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Kawaguchi-Shi, Japan

Sanofi-Aventis Investigational Site Number 392002

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Kita-Ku, Japan

Sanofi-Aventis Investigational Site Number 392005

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Yokohama-Shi, Japan

Sanofi-Aventis Investigational Site Number 392006

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Yokohama-Shi, Japan

Sanofi-Aventis Investigational Site Number 392012

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Kanazawa-Shi, Japan

Sanofi-Aventis Investigational Site Number 392011

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Kofu-Shi, Japan

Sanofi-Aventis Investigational Site Number 392014

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Obu-Shi, Japan

Sanofi-Aventis Investigational Site Number 392010

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Yokohama-Shi, Japan

Sanofi-Aventis Investigational Site Number 392007

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Yokohama-Shi, Japan

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