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
| Type | Name | Description |
|---|---|---|
| DRUG | Sublingual tablet of ragweed pollen allergen extract | administered 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.