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Terminated Phase 1 Interventional Results available

Pharmacokinetics and Safety of Ceftobiprole in Neonates and Infants up to 3 Months Treated With Systemic Antibiotics

ClinicalTrials.gov ID: NCT02527681

Public ClinicalTrials.gov record NCT02527681. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 5, 2026, 7:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

An Open-label Study to Evaluate the Single-dose Pharmacokinetics and Safety of Ceftobiprole in Neonate and Infant Subjects Aged up to 3 Months Undergoing Treatment With Systemic Antibiotics

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This study characterized the pharmacokinetics and safety of a single dose of ceftobiprole in neonates and infants aged ≤ 3 months.

Study identification

NCT ID
NCT02527681
Recruitment status
Terminated
Study type
Interventional
Phase
Phase 1
Lead sponsor
Basilea Pharmaceutica
Industry
Enrollment
15 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
Up to 3 Months
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 21, 2016
Primary completion
Feb 24, 2020
Completion
Feb 24, 2020
Last update posted
Jun 4, 2023

2016 – 2020

United States locations

U.S. sites
9
U.S. states
7
U.S. cities
8
Facility City State ZIP Site status
Loma Linda University Medical Center Loma Linda California 92354
University of Southern California Los Angeles California 90089
University of California Los Angeles Los Angeles California 90095
Beacon Children's Hospital South Bend Indiana 46601
Norton Children's Hospital Louisville Kentucky 40202
Duke University Hospital Durham North Carolina 27705
University of Pittsburgh Medical Center Cancer Center at Magee-Womens Hospital Pittsburgh Pennsylvania 15224
The University of Texas Health Science Center at Houston Houston Texas 77030
West Virginia University School of Medicine Morgantown West Virginia 26506-9214

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 5 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT02527681, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 4, 2023 · Synced Sep 5, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT02527681 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →