Completed

Safety and Pharmacokinetics of Micafungin in Children Supported With Extracorporeal Membrane Oxygenation

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What is being tested

Micafungin

+ Micafungin

+ Micafungin

Drug
Who is being recruted

Invasive Fungal Infections+3

+ Bacterial Infections and Mycoses

+ Candidiasis

Until 18 Years
+9 Eligibility Criteria
See all eligibility criteria
How is the trial designed

Treatment Study

Phase 1
Interventional
Study Start: January 2013
See protocol details

Summary

Principal SponsorKevin Watt
Last updated: November 5, 2019
Sourced from a government-validated database.Claim as a partner

Study start date: January 1, 2013

Actual date on which the first participant was enrolled.

Extracorporeal membrane oxygenation (ECMO) is a cardiopulmonary bypass device that provides life-saving, complete respiratory and cardiac support for children who suffer refractory heart or lung failure. While on ECMO, children are at increased risk of infection, including fungal infection. Antifungal prophylaxis can potentially reduce the burden of disease in children on ECMO. Because fungal infections can result in biofilms that are difficult to treat, treatment includes not only antifungal medications but also removal of any large intravenous lines. However, catheter removal for children on ECMO is impossible; therefore, therapy relies upon optimal antifungal management alone. Micafungin is an antifungal medication that works well against the most common fungal infections and has been shown to be safe in children. Micafungin may be particularly efficacious in children on ECMO because of the drug's ability to penetrate biofilms. However, the ECMO circuit is known to substantially alter drug levels for many drugs, resulting in important dosing changes. Appropriate micafungin dosing in this setting is unknown and sub-optimal dosing might result in therapeutic and prophylactic failure. Standard dosing of micafungin are 4 and 2 mg per kilogram of body weight given intravenously once daily for treatment and prophylaxis, respectively. Based on preliminary data and modeling from other studies, investigators hypothesize that 8 and 4 mg per kilogram given once daily will achieve proper drug levels to respectively treat and prevent fungal infections in children under 2 years of age who are supported by ECMO. Because the ECMO circuit should have less of an impact on volume of distribution in larger children, investigators hypothesize that in children from 2 to 18 years old, standard dosing of micafungin will achieve proper drug concentrations. Investigators hold the FDA investigational new drug application (IND #115255) to give micafungin to children on ECMO at the doses described above. Blood samples will be collected at specific times around the first and fourth micafungin doses to describe the pharmacokinetics and drug extraction by the ECMO circuit.

Principal SponsorKevin Watt
Last updated: November 5, 2019
Sourced from a government-validated database.Claim as a partner

Protocol

This section provides details of the study plan, including how the study is designed and what the study is measuring.
Design Details

18 patients to be enrolled

Total number of participants that the clinical trial aims to recruit.

Treatment Study

These studies test new ways to treat a disease, condition, or health issue. The goal is to see if a new drug, therapy, or approach works better or has fewer side effects than existing options.



Eligibility

Researchers look for people who fit a certain description, called eligibility criteria: person's general health condition or prior treatments.
Conditions
Criteria

Any sex

Biological sex of participants that are eligible to enroll.

Until 18 Years

Range of ages for which participants are eligible to join.

Healthy volunteers not allowed

If individuals who are healthy and do not have the condition being studied can participate.

Conditions

Pathology

Invasive Fungal InfectionsBacterial Infections and MycosesCandidiasisInfectionsMycosesCandidiasis, Invasive

Criteria

5 inclusion criteria required to participate
= 17.85 years at the time of enrollment

Availability and willingness of the parent/legal guardian to provide written informed consent

For treatment dosing arm: confirmed or suspected infection

Sufficient venous access to permit administration of study medication

Show More Criteria

4 exclusion criteria prevent from participating
Any other concomitant condition, which in the opinion of the investigator would preclude a subject's participation in the study

Pregnancy

Previous participation in this study

Subject with a history of anaphylaxis attributed to an echinocandin

Study Plan

Find out more about all the medication administered in this study, their detailed description and what they involve.
Treatment Groups
Study Objectives

3 intervention groups are designated in this study

This study does not include a placebo group 

Treatment Groups

Group I

Age group: 0 - <2y, Micafungin 8 mg/kg/day IV

Group II

Age group: 0-<2y, Micafungin 4 mg/kg/day IV

Group III

Age group: 2-17.85 y, Micafungin standard of care dosing (decided by treating physician)

Study Objectives

Primary Objectives

Secondary Objectives

Study Centers

These are the hospitals, clinics, or research facilities where the trial is being conducted. You can find the location closest to you and its status.

This study has 1 location

Duke University Medical Center

Durham, United StatesOpen Duke University Medical Center in Google Maps
CompletedOne Study Center