Viewing Study NCT05335005


Ignite Creation Date: 2025-12-25 @ 3:15 AM
Ignite Modification Date: 2025-12-26 @ 1:54 AM
Study NCT ID: NCT05335005
Status: COMPLETED
Last Update Posted: 2024-10-17
First Post: 2022-04-12
Is NOT Gene Therapy: False
Has Adverse Events: True

Brief Title: MK-2060 and Clopidogrel Co-administration Safety and Tolerability Study in Participants With End-Stage Renal Disease (ESRD) (MK-2060-008)
Sponsor: Merck Sharp & Dohme LLC
Organization:

Study Overview

Official Title: A Study to Evaluate Safety and Tolerability of Co-administration of MK-2060 and Clopidogrel in Participants With End-Stage Renal Disease on Hemodialysis
Status: COMPLETED
Status Verified Date: 2024-07
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: MK-2060 is being developed for prevention of thrombotic complications in end-stage renal disease (ESRD). The purpose of this study is to conduct a preliminary evaluation of the safety and tolerability of MK-2060 treatment in combination with a commonly used P2Y12 receptor inhibitor, clopidogrel, in ESRD patients.
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?: None
Is an FDA AA801 Violation?:

Secondary ID Infos

Secondary ID Type Domain Link View
MK-2060-008 OTHER Merck View
2021-005333-17 EUDRACT_NUMBER None View