Viewing Study NCT01733069


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Study NCT ID: NCT01733069
Status: COMPLETED
Last Update Posted: 2014-01-14
First Post: 2012-11-20
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: Clinical Evaluation of the APTIMA® COMBO 2® Assay Using the PANTHER™ System
Sponsor: Gen-Probe, Incorporated
Organization:

Study Overview

Official Title: Clinical Evaluation of the APTIMA® COMBO 2®Assay Using the PANTHER™ System
Status: COMPLETED
Status Verified Date: 2013-11
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 objectives of this study are to establish the performance characteristics of the AC2 (APTIMA Combo 2) Assay on the PANTHER System for the sample types cleared for use on the TIGRIS and DTS (Direct Tube Sampling) Systems and to demonstrate the repeatability and reproducibility of the AC2 Assay on the PANTHER System.
Detailed Description: The results of this protocol AC2PS-US11-001 (NCT01733069) are based on samples collected from protocol ACTPS-US10-001(NCT01358799).

The registration for NCT01358799 was withdrawn because the samples were not tested under protocol ACTPS-US10-001, instead they were tested under the protocol registered here AC2PS-US11-001 (NCT01733069).

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?:

Secondary ID Infos

Secondary ID Type Domain Link View
ACTPS-US10-001 OTHER Gen-Probe View