Viewing Study NCT06609161



Ignite Creation Date: 2024-10-26 @ 3:41 PM
Last Modification Date: 2024-10-26 @ 3:41 PM
Study NCT ID: NCT06609161
Status: COMPLETED
Last Update Posted: None
First Post: 2024-09-20

Brief Title: A Study to Compare Oral Formulations of Tedizolid Phosphate in Healthy Adults MK-1986-044
Sponsor: None
Organization: None

Study Overview

Official Title: A Study to Evaluate the Definitive Bioequivalence of Tedizolid Phosphate Single-Unit-Dose Sachet Powder for Oral Suspension Compared to Tedizolid Phosphate Powder for Oral Suspension Bottle Used in Pediatric Clinical Studies
Status: COMPLETED
Status Verified Date: 2024-09
Last Known Status: None
Delayed Posting: No
If Stopped, Why?: Not Stopped
Has Expanded Access: No
If Expanded Access, NCT#: N/A
Has Expanded Access, NCT# Status: N/A
Acronym: None
Brief Summary: The goal of the study is to learn what happens to different oral formulations of tedizolid phosphate MK-1986 in a healthy persons body over time Researchers want to know if there is a difference in the oral formulations absorption and elimination from the healthy persons body
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