Clinical trial

Safety and Efficacy of a Sublingual Specific Immunotherapy With an Extract of a…

NCT00264459 · Allergopharma GmbH & Co. KG, Industry · Completed

Key facts

NCT number NCT00264459
Title Safety and Efficacy of a Sublingual Specific Immunotherapy With an Extract of a Six Grass Pollen Mixture
Official title A Multicentre, Placebo-controlled, Double-blind Study to Evaluate Efficacy and Safety of a Perennial Sublingual Specific Immunotherapy With a Liquid Formulation of an Extract of a Six Grass Pollen-mixture in Patients With Clinically Relevant Grass Pollen Sensitivity.
Lead sponsor Allergopharma GmbH & Co. KG, Industry
Status Completed
Phase Phase 3
Study type Interventional
Conditions Grass Pollen Allergy
Intervention type Biological, Other
Interventions Grass pollen formulation, Comparator
Enrollment 160
Start date Feb 1, 2003
Primary completion Aug 1, 2008
Completion Sep 1, 2011
First posted Dec 13, 2005
Last update posted Jan 24, 2014
Countries Germany

At a glance

  • 1–9 Study sites
  • No Results posted
  • None Linked FDA submissions

Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.

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Source: U.S. National Library of Medicine (NLM), ClinicalTrials.gov · Source date:

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