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Open, Pharmacokinetic Study of Caspofungin in Neonates and Infants (0991-058)

Primary Purpose

Candidiasis

Status
Completed
Phase
Phase 2
Locations
Study Type
Interventional
Intervention
caspofungin acetate
Sponsored by
Merck Sharp & Dohme LLC
About
Eligibility
Locations
Outcomes
Full info

About this trial

This is an interventional treatment trial for Candidiasis

Eligibility Criteria

undefined - 3 Months (Child)All SexesDoes not accept healthy volunteers

Inclusion Criteria: Neonates and infants <3 months of age Patient has a body weight greater than or equal to 500 grams Patient has documented or highly suspected Candida infection Exclusion Criteria: Patient is greater than 3 months of age Patient has a body weight of less than 500 grams Patient does not meet certain laboratory testing criteria Patient is hemodynamically unstable, exhibits hemodynamic compromise or is not expected to survive at least 5 days Patient has documented HIV infection of any stage Patient has a history of allergy, hypersensitivity, or serious reaction to caspofungin or another member of the echinocandin class

Sites / Locations

    Outcomes

    Primary Outcome Measures

    Pharmacokinetic parameters of drug exposure

    Secondary Outcome Measures

    Safety and tolerability

    Full Information

    First Posted
    May 24, 2006
    Last Updated
    February 20, 2017
    Sponsor
    Merck Sharp & Dohme LLC
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    1. Study Identification

    Unique Protocol Identification Number
    NCT00330395
    Brief Title
    Open, Pharmacokinetic Study of Caspofungin in Neonates and Infants (0991-058)
    Official Title
    A Multicenter, Sequential-Panel, Open-Label, Noncomparative Study to Investigate the Safety, Tolerability, and Pharmacokinetics of Caspofungin Acetate in Neonates and Infants Less Than 3 Months of Age.
    Study Type
    Interventional

    2. Study Status

    Record Verification Date
    February 2017
    Overall Recruitment Status
    Completed
    Study Start Date
    May 2006 (undefined)
    Primary Completion Date
    October 2006 (Actual)
    Study Completion Date
    October 2006 (Actual)

    3. Sponsor/Collaborators

    Responsible Party, by Official Title
    Sponsor
    Name of the Sponsor
    Merck Sharp & Dohme LLC

    4. Oversight

    5. Study Description

    Brief Summary
    The purpose of this study is to test the amount of caspofungin found in the blood of neonate and infants <3 months of age following treatment with caspofungin at 25 mg/m2. Another purpose is to test the safety of caspofungin in treating neonates and infants with Candida infections (a certain type of fungal infection).

    6. Conditions and Keywords

    Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
    Candidiasis

    7. Study Design

    Primary Purpose
    Treatment
    Study Phase
    Phase 2
    Interventional Study Model
    Single Group Assignment
    Masking
    None (Open Label)
    Allocation
    Non-Randomized
    Enrollment
    16 (Actual)

    8. Arms, Groups, and Interventions

    Intervention Type
    Drug
    Intervention Name(s)
    caspofungin acetate
    Other Intervention Name(s)
    MK0991
    Intervention Description
    Duration of Treatment 28 Days
    Primary Outcome Measure Information:
    Title
    Pharmacokinetic parameters of drug exposure
    Secondary Outcome Measure Information:
    Title
    Safety and tolerability

    10. Eligibility

    Sex
    All
    Maximum Age & Unit of Time
    3 Months
    Accepts Healthy Volunteers
    No
    Eligibility Criteria
    Inclusion Criteria: Neonates and infants <3 months of age Patient has a body weight greater than or equal to 500 grams Patient has documented or highly suspected Candida infection Exclusion Criteria: Patient is greater than 3 months of age Patient has a body weight of less than 500 grams Patient does not meet certain laboratory testing criteria Patient is hemodynamically unstable, exhibits hemodynamic compromise or is not expected to survive at least 5 days Patient has documented HIV infection of any stage Patient has a history of allergy, hypersensitivity, or serious reaction to caspofungin or another member of the echinocandin class
    Overall Study Officials:
    First Name & Middle Initial & Last Name & Degree
    Medical Monitor
    Organizational Affiliation
    Merck Sharp & Dohme LLC
    Official's Role
    Study Director

    12. IPD Sharing Statement

    Citations:
    PubMed Identifier
    19075070
    Citation
    Saez-Llorens X, Macias M, Maiya P, Pineros J, Jafri HS, Chatterjee A, Ruiz G, Raghavan J, Bradshaw SK, Kartsonis NA, Sun P, Strohmaier KM, Fallon M, Bi S, Stone JA, Chow JW. Pharmacokinetics and safety of caspofungin in neonates and infants less than 3 months of age. Antimicrob Agents Chemother. 2009 Mar;53(3):869-75. doi: 10.1128/AAC.00868-08. Epub 2008 Dec 15.
    Results Reference
    background
    Available IPD and Supporting Information:
    Available IPD/Information Type
    CSR Synopsis
    Available IPD/Information URL
    http://www.merck.com/clinical-trials/policies-perspectives.html

    Learn more about this trial

    Open, Pharmacokinetic Study of Caspofungin in Neonates and Infants (0991-058)

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