Viewing Study NCT01191359


Ignite Creation Date: 2025-12-24 @ 2:35 PM
Ignite Modification Date: 2026-02-22 @ 5:22 PM
Study NCT ID: NCT01191359
Status: COMPLETED
Last Update Posted: 2013-02-08
First Post: 2010-08-27
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Efficacy and Tolerability of Two Different Administration Routes With SLITonePLUS Birch
Sponsor: ALK-Abelló A/S
Organization:

Study Overview

Official Title: A Multicentre Randomised Phase II Clinical Pilot Study to Compare the Pharmacodynamic Efficacy and Tolerability of the Sublingual and the Vestibular Administration Route for SLITonePLUS® Birch
Status: COMPLETED
Status Verified Date: 2013-02
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: False
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: Multicentre Phase II trial, comparing two different administration routes of SLITonePLUS Birch in regard to pharmacodynamic efficacy and tolerability.
Detailed Description: None

Study Oversight

Has Oversight DMC: False
Is a FDA Regulated Drug?: None
Is a FDA Regulated Device?: None
Is an Unapproved Device?: None
Is a PPSD?: None
Is a US Export?: None
Is an FDA AA801 Violation?: