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Trials / Completed

CompletedNCT01224834

Safety and Tolerability Study of Ragweed SLIT Tablets

Phase I Study to Investigate the Safety, Tolerability and Pharmacodynamic Effects of Sublingual Immunotherapy Tablets Given in Single Rising Doses and in Multi Dose Regimens to Subjects With an Allergy to Ragweed Pollen.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
60 (actual)
Sponsor
Stallergenes Greer · Industry
Sex
All
Age
18 Years – 60 Years
Healthy volunteers
Not accepted

Summary

The purpose of this study is to determine the safety and tolerability of several doses of ragweed pollen allergen extract administered as sublingual tablets in subjects with allergic rhinitis to ragweed.

Conditions

Interventions

TypeNameDescription
DRUGSublingual tablet of ragweed pollen allergen extractadministered once a day over 10 days

Timeline

Start date
2009-01-01
Primary completion
2009-04-01
Completion
2009-10-01
First posted
2010-10-20
Last updated
2010-11-08

Locations

1 site across 1 country: Hungary

Source: ClinicalTrials.gov record NCT01224834. Inclusion in this directory is not an endorsement.

Safety and Tolerability Study of Ragweed SLIT Tablets (NCT01224834) · Clinical Trials Directory