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Search / Trial NCT00574379

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

Launched by FAES FARMA, S.A. · Dec 14, 2007

Trial Information

Current as of September 10, 2025

Completed

Keywords

Allergic Rhinitis Mountain Cedar Pollen Pollen Allergy Rhinoconjunctivitis

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • clinical history of Seasonal Allergic Rhinoconjunctivitis with seasonal onset and offset of nasal allergy symptoms
  • documentation of a positive skin test within one year of screening to Mountain Cedar allergen
  • Exclusion Criteria:
  • significant medical condition
  • significant nasal abnormality
  • significant cardiac condition
  • recent infection
  • use of other allergy medication during the study

About Faes Farma, S.A.

Faes Farma, S.A. is a leading pharmaceutical company based in Spain, dedicated to the research, development, manufacturing, and commercialization of innovative healthcare solutions. With a robust portfolio that spans various therapeutic areas, including neurology, dermatology, and respiratory diseases, Faes Farma is committed to improving patient outcomes through high-quality medicines. The company emphasizes a strong focus on clinical research and collaboration, aiming to advance medical knowledge and deliver safe and effective treatments globally. Through its dedication to excellence and innovation, Faes Farma plays a pivotal role in the evolving landscape of modern medicine.

Locations

San Antonio, Texas, United States

Oklahoma City, Oklahoma, United States

San Antonio, Texas, United States

Austin, Texas, United States

San Antonio, Texas, United States

San Antonio, Texas, United States

Waco, Texas, United States

Waco, Texas, United States

Austin, Texas, United States

Austin, Texas, United States

Kerrville, Texas, United States

San Antonio, Texas, United States

San Antonio, Texas, United States

Patients applied

0 patients applied

Trial Officials

Ander Sologuren, MD

Study Director

Faes Farma, S.A.

Paul Ratner, MD

Principal Investigator

Sylvana Research Associates

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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