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Fexofenadine Study On Filipino Children for The Relief of Perennial And Intermittent Allergic Rhinitis

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Sanofi

Status and phase

Completed
Phase 4

Conditions

Rhinitis, Allergic, Perennial

Treatments

Drug: Fexofenadine

Study type

Interventional

Funder types

Industry

Identifiers

NCT00741897
M016455C_4001

Details and patient eligibility

About

To determine the safety and efficacy of Fexofenadine (Telfast®) 30mg pediatric tablets on Filipino children aged 6 to 11 for the relief of symptoms associated with perennial and intermittent allergic rhinitis.

Enrollment

264 patients

Sex

All

Ages

6 to 11 years old

Volunteers

No Healthy Volunteers

Inclusion and exclusion criteria

Inclusion Criteria:

  • Children who manifest allergic rhinitis symptoms such as sneezing, rhinorrhea, itchy nose/palate/throat and/or itchy/watery/red eyes.

Trial design

Primary purpose

Treatment

Allocation

N/A

Interventional model

Single Group Assignment

Masking

None (Open label)

264 participants in 1 patient group

1
Experimental group
Description:
Fexofenadine
Treatment:
Drug: Fexofenadine

Trial contacts and locations

1

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Data sourced from clinicaltrials.gov

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