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Completed Phase 2 Interventional

Efficacy, Safety and PK of Once or Twice Daily Bilastine (10 or 20 mg) Compared With Placebo in the Symptomatic Treatment of SAR

ClinicalTrials.gov ID: NCT00574379

Public ClinicalTrials.gov record NCT00574379. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 20, 2026, 1:48 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-Center Randomized, Double-Blind, Placebo-Controlled, Parallel Study to Evaluate the Efficacy, Safety and Pharmacokinetics of Once or Twice Daily Bilastine (10 or 20 mg) Compared With Placebo Given Orally in The Treatment of the Symptoms of Seasonal Allergic Rhino-Conjunctivitis With Allergy to Mountain Cedar Pollen

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Evaluate the relative efficacy of four dosing regimens of bilastine tablets (given either once or twice per day) versus placebo in patients with Seasonal Allergic Rhinitis (SAR) in the Mountain Cedar season in south Texas and Oklahoma based on the mean change from baseline in Reflective Total Nasal Symptom Scores (TNSS) assessed over 14 days of treatment.

Study identification

NCT ID
NCT00574379
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Faes Farma, S.A.
Industry
Enrollment
805 participants

Conditions and interventions

Eligibility (public fields only)

Age range
12 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Dec 2007 (Type not available)
Primary completion
Mar 2008 (Actual)
Completion
Mar 2008 (Actual)
Last update posted
Feb 15, 2019

2007 – 2008

United States locations

U.S. sites
13
U.S. states
2
U.S. cities
5
Facility City State ZIP Site status
Oklahoma Allergy and Asthma Clinic Oklahoma City Oklahoma 73104 —
MetaClin Research Inc. Austin Texas 78704 —
Austin Clinical Research Austin Texas 78750 —
Lovelace Scientific Resources Austin Texas 78759 —
Kerrville Research Associates Kerrville Texas 78028-6071 —
Biogenics Research Institute San Antonio Texas 78229 —
DGD Research San Antonio Texas 78229 —
Diagnostics Research Group San Antonio Texas 78229 —
Southwest Allergy and Asthma Centre San Antonio Texas 78229 —
Sylvana Research Associates San Antonio Texas 78229 —
Live Oak Allergy and Asthma San Antonio Texas 78233 —
Allergy & Asthma Care of Waco Waco Texas 76708 —
Allergy Asthma Research Institute Waco Texas 76712 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT00574379, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Feb 15, 2019 · Synced Oct 20, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT00574379 live on ClinicalTrials.gov.

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