Viewing Study NCT06008457


Ignite Creation Date: 2025-12-24 @ 6:52 PM
Ignite Modification Date: 2026-01-05 @ 5:38 PM
Study NCT ID: NCT06008457
Status: COMPLETED
Last Update Posted: 2025-06-25
First Post: 2023-08-21
Is NOT Gene Therapy: True
Has Adverse Events: False

Brief Title: Evaluation of the Labcorp COVID-19+Flu+RSV Test Home Collection Kit
Sponsor: Sequenom, Inc.
Organization:

Study Overview

Official Title: Prospective Clinical Evaluation of the Labcorp COVID-19+Flu+RSV Test Home Collection Kit as Offered Commercially by Labcorp - A Registry Study
Status: COMPLETED
Status Verified Date: 2025-06
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: To compare the results obtained by analysis of a self-collected anterior nasal (AN) swab as part of the Labcorp COVID-19+Flu+RSV Test Home Collection Kit to a healthcare provider (HCP)-collected AN swab in patients with symptoms of viral respiratory infection consistent with influenza A (Flu A), influenza B (Flu B), respiratory syncytial virus (RSV) and/or SARS-CoV-2 (C-19).
Detailed Description: None

Study Oversight

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