Viewing Study NCT01700192



Ignite Creation Date: 2024-05-06 @ 12:58 AM
Last Modification Date: 2024-10-26 @ 10:57 AM
Study NCT ID: NCT01700192
Status: COMPLETED
Last Update Posted: 2017-09-15
First Post: 2012-10-02

Brief Title: Efficacy and Safety Study of SCH 900237MK-8237 in Children and Adults With House Dust Mite-Induced Allergic RhinitisRhinoconjunctivitis P05607
Sponsor: ALK-Abelló AS
Organization: ALK-Abelló AS

Study Overview

Official Title: A One-year Placebo-Controlled Study Evaluating the Efficacy and Safety of the House Dust Mite Sublingual Allergen Immunotherapy Tablet SCH 900237MK 8237 in Children and Adult Subjects With House Dust Mite-Induced Allergic RhinitisRhinoconjunctivitis With or Without Asthma Protocol No P05607001
Status: COMPLETED
Status Verified Date: 2017-09
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: The purpose of this study is to assess the efficacy and safety of MK-8237 SCH 900237 in the treatment of House Dust Mite HDM-Induced Allergic RhinitisRhinoconjunctivitis ARARC in children and adults

The primary hypothesis of this study is that administration of MK-8237 compared to placebo results in significant reduction in the average total combined rhinitis score TCRS
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-8237-001 OTHER Merck Protocol ID None