Viewing Study NCT05309304


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Ignite Modification Date: 2025-12-25 @ 7:06 PM
Study NCT ID: NCT05309304
Status: COMPLETED
Last Update Posted: 2022-10-12
First Post: 2022-03-25
Is NOT Gene Therapy: False
Has Adverse Events: False

Brief Title: Cefazolin PK Study 3g vs 2g
Sponsor: Baxter Healthcare Corporation
Organization:

Study Overview

Official Title: Pharmacokinetic Study of Cefazolin 3 g/150 mL in Subjects Weighing Greater Than or Equal to 120 kg Versus Cefazolin 2 g/100 mL in Subjects Weighing Less Than 120 kg
Status: COMPLETED
Status Verified Date: 2022-10
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: Study is to characterize the safety and tolerability of cefazolin after a single IV administration in healthy subjects in a 3 g/150 mL presentation to meet the increasing clinical need for the indication of perioperative prophylaxis in this patient population weighing greater than or equal to (≥) 120 kg.
Detailed Description: None

Study Oversight

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