Assessment of the Pharmacokinetics and Safety of ANT3310 Combined With Meropenem in Renally Impaired Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

July 19, 2024

Primary Completion Date

July 3, 2025

Study Completion Date

July 10, 2025

Conditions
Renal Impairment
Interventions
DRUG

ANT3310

ANT3310 will be administered as a single intravenous infusion over 3 hours at a constant rate.

DRUG

Meropenem

meropenem will be administered as a single intravenous infusion over 3 hours at a constant rate.

Trial Locations (1)

D-24105

CRS Clinical Research Services Kiel GmbH, Kiel

Sponsors

Lead Sponsor

All Listed Sponsors
collaborator

Clinical Research Center Kiel GmbH

OTHER

lead

Antabio

INDUSTRY