Viewing Study NCT01469182



Ignite Creation Date: 2024-05-06 @ 12:00 AM
Last Modification Date: 2024-10-26 @ 10:43 AM
Study NCT ID: NCT01469182
Status: COMPLETED
Last Update Posted: 2017-03-03
First Post: 2011-10-21

Brief Title: A Study of Ragweed Ambrosia Artemisiifolia Allergy Immunotherapy Tablet in Adults With Ragweed Allergies P05751
Sponsor: ALK-Abelló AS
Organization: ALK-Abelló AS

Study Overview

Official Title: A 28-Day Study Evaluating the Safety of Ragweed Ambrosia Artemisiifolia Allergy Immunotherapy Tablet SCH 39641MK-3641 Treatment in Ragweed Allergic Adults Phase 3 Protocol NoP05751
Status: COMPLETED
Status Verified Date: 2017-01
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: This study assessed the safety profile of short ragweed Ambrosia artemisiifolia in participants with ragweed-induced rhinoconjunctivitis with or without asthma The primary objective was to compare treatment-emergent adverse events AEs for participants treated with short ragweed allergy immunotherapy tablet AIT with those treated with placebo
Detailed Description: None

Study Oversight

Has Oversight DMC: None
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?: None
Secondary IDs
Secondary ID Type Domain Link
MK-3641 OTHER Merck None