Population Pharmacokinetics of Amoxicillin in Neonates
NCT03987100 · Status: UNKNOWN · Type: OBSERVATIONAL · Enrollment: 200
Last updated 2019-06-14
Summary
The objective of NEOPOPI is to conduct a population pharmacokinetic study of amoxicillin in neonates, in order to evaluate and optimize neonatal dose regimen.
There will be no change to the medication treatment received by participants. An opportunistic pharmacokinetic sampling approach will be followed: samples will be scavenged from blood or cerebrospinal fluid drawn for routine biochemical tests. In this way, no additional invasive tests will be needed.
Conditions
- Emergencies
Sponsors & Collaborators
-
Rennes University Hospital
lead OTHER
Eligibility
- Max Age
- 44 Weeks
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2019-02-05
- Primary Completion
- 2021-08-31
- Completion
- 2021-08-31
Countries
- France
Study Locations
More Related Trials
-
Auranofin PK Following Oral Dose Administration
NCT02089048 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics and Pharmacodynamics of Two Prolonged-release Formulations of Vamifeport in Healthy Adults
NCT06726863 ·Status: COMPLETED ·Phase: PHASE1
-
Open Label Study of a Single Dose of a New Extended Long Acting Formulation of Octreotide Pamoate in Healthy Volunteers
NCT00432068 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics Study of Nemonoxacin Malate Capsules in Subjects With Moderate Impaired Hepatic Function
NCT02604498 ·Status: COMPLETED ·Phase: PHASE1
-
Observational Study Evaluating The Processing Or Breakdown Of GW679769 In Subjects With Hepatic Impairment
NCT00359177 ·Status: COMPLETED ·Phase: PHASE1
-
AMAP102 - Safety, Tolerability and Pharmacokinetics in Healthy Subjects
NCT00995605 ·Status: TERMINATED ·Phase: PHASE1
-
A Biopharmaceutics Study to Assess the Pharmacokinetics of Single Oral and IV Doses of Olorofim
NCT04207957 ·Status: COMPLETED ·Phase: PHASE1
-
Japanese Pharmacokinetic Bridging Study for CC-93538
NCT04096105 ·Status: COMPLETED ·Phase: PHASE1
-
Nitazoxanide Pharmacokinetic Parameters in Hepatic Impaired Patients
NCT05116826 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of OP-101 After Intravenous Administration in Healthy Volunteers
NCT03500627 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics of Liposomal Amphotericin B in Critically Ill vs. Non-critically Ill Hematological Patients: Exploration of Covariates
NCT03529617 ·Status: RECRUITING
-
Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics Investigation of GSK3335065 Intravenous (IV) Infusion in Healthy Adults
NCT03245619 ·Status: TERMINATED ·Phase: PHASE1
-
Nitazoxanide Pharmacokinetic Parameters in Renal Impaired Subjects
NCT05368935 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic Study on G1090N (Nitazoxanide) Capsules in Healthy Volunteers
NCT07110441 ·Status: COMPLETED ·Phase: PHASE1
-
A Study on the Effect of Renal Function on the Pharmacakokinetics of RO5024048 (Parent of Prodrug RO5024048) Following Multiple Oral Dose Administration of RO5024048
NCT01099904 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics, Safety, and Tolerability of Various XW10172 Oral Formulations in Healthy Adult Volunteers
NCT04688580 ·Status: COMPLETED ·Phase: EARLY_PHASE1
-
Absorption, Distribution, Metabolism And Excretion Study For GSK221149A
NCT00457925 ·Status: COMPLETED ·Phase: PHASE1
-
Monitoring the Hyperammonaemia:TOXicity of Drugs (AmmoTOX)
NCT03947034 ·Status: COMPLETED
-
A Phase 1, Multicenter, Open-Label Study to Evaluate the Effect of Mild or Moderate Hepatic Impairment on the Multiple-Dose Pharmacokinetics of Ozanimod
NCT04639115 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics of XNW4107 in Subjects With Various Degrees of Renal Function
NCT04787562 ·Status: COMPLETED ·Phase: PHASE1
-
Study in Healthy Volunteers to Investigate the Effects of Quinidine on the Pharmacokinetics of NKTR-118
NCT01533155 ·Status: COMPLETED ·Phase: PHASE1
-
Phase 1 Absorption Distribution Metabolism and Excretion of AQX-1125
NCT03185195 ·Status: COMPLETED ·Phase: PHASE1
-
A Study Investigating the Excretion Balance, Pharmacokinetics and Metabolism of a Single Oral Dose of [14C]-Labeled Risdiplam (RO7034067) in Healthy Male Participants
NCT03036501 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetics (PK) of Ertapenem Intravenous (IV) Bolus Versus Standard Infusion
NCT01148771 ·Status: COMPLETED ·Phase: PHASE4
-
Target Site Pharmacokinetics of Doripenem After a Single Dose of 500mg in Healthy Volunteers Dori_MD_1
NCT01311141 ·Status: COMPLETED ·Phase: PHASE4