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Clinical Trial Summary

The purpose of this study is to determine whether the oral administration of grass pollen peptides is safe and effective in the treatment of allergic rhinitis.


Clinical Trial Description

n/a


Study Design

Allocation: Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Parallel Assignment, Masking: Double Blind (Subject, Caregiver, Investigator, Outcomes Assessor), Primary Purpose: Treatment


Related Conditions & MeSH terms


NCT number NCT00833066
Study type Interventional
Source BioTech Tools S.A.
Contact
Status Completed
Phase Phase 1/Phase 2
Start date February 2009
Completion date November 2009

See also
  Status Clinical Trial Phase
Completed NCT01111279 - Clinical Safety and Tolerability Study of gpASIT+TM and gpASIT+TM/Immunoregulating Adjuvant to Treat Seasonal Grass Pollen Rhinoconjunctivitis Phase 1
Completed NCT00813046 - Safety and Tolerance Study of Grass Pollen-derived Peptides to Treat Allergic Rhinitis Phase 1
Completed NCT02761252 - Efficacy of Co-administration of Bilastine and Montelukast in Patients With SARC and Asthma Phase 4