Comparison of Candida Eradication and Serum Cidal Activity of Echinocandins
Primary Purpose
Candidemia
Status
Completed
Phase
Phase 4
Locations
United States
Study Type
Interventional
Intervention
micafungin
Micafungin
Caspofungin
Sponsored by
About this trial
This is an interventional treatment trial for Candidemia focused on measuring candidemia, echinocandin, micafungin, caspofungin
Eligibility Criteria
Inclusion Criteria:
- Adult patients with presumptive candidemia
Exclusion Criteria:
- Patients with severe neutropenia (<500)
- Patients with APACHE II scores > 20
- Patients with severe liver disease
Sites / Locations
- Sparrow Hospital
Arms of the Study
Arm 1
Arm 2
Arm 3
Arm Type
Active Comparator
Active Comparator
Active Comparator
Arm Label
micafungin 100
micafungin 200
Caspofungin
Arm Description
Patients receive Micafungin 100 mg qd
Patients receive 200 mg Micafungin qd
Patients receive caspofungin 70 mg LD followed by 50 mg qd
Outcomes
Primary Outcome Measures
Serum Cidal Activity as Tested Against Various Candida Isolates and Reported as Ex-vivo Effect (Log Inhibition of Growth)
Serum cidal activity of serum collected at different timepoints from the patients will be tested against various Candida isolates and the ex-vivo effect reported as log inhibition (logrithmic measurement of the decrease in microbiological growth).
These Candida isolates had a range of minimum inhibitory concentrations (MIC) to Caspofungin (C) and Micafungin (M).
Secondary Outcome Measures
Full Information
NCT ID
NCT00839540
First Posted
February 6, 2009
Last Updated
February 27, 2012
Sponsor
Gary E. Stein, Pharm.D.
Collaborators
Astellas Pharma US, Inc.
1. Study Identification
Unique Protocol Identification Number
NCT00839540
Brief Title
Comparison of Candida Eradication and Serum Cidal Activity of Echinocandins
Official Title
Comparison of Candida Eradication and Serum Cidal Activity of Echinocandins in Patients With Presumptive Candidemia
Study Type
Interventional
2. Study Status
Record Verification Date
February 2012
Overall Recruitment Status
Completed
Study Start Date
December 2008 (undefined)
Primary Completion Date
May 2010 (Actual)
Study Completion Date
May 2010 (Actual)
3. Sponsor/Collaborators
Responsible Party, by Official Title
Sponsor-Investigator
Name of the Sponsor
Gary E. Stein, Pharm.D.
Collaborators
Astellas Pharma US, Inc.
4. Oversight
Data Monitoring Committee
No
5. Study Description
Brief Summary
The purpose of this pharmacokinetic (PK) and pharmacodynamic (PD) study is:
To study the rate and duration of serum cidal activity of caspofungin (CFG) and micafungin (MFG) against Candida isolates from the subject and against Candida glabrata with varying degrees of caspofungin susceptibilities.
This investigation will provide clinicians information supporting the use of caspofungin and micafungin in situations where Candida strains may be a cause of infection.
Detailed Description
Methods:
Patients - Adult patients with presumptive candidemia. Patients with severe neutropenia (<500) APACHE II scores > 20, or significant liver disease will be excluded. All will give written informed consent (Pappas et al. CID. Oct 1, 2007).
Drugs - Patients will receive either CFG: 70 mg loading dose (LD) followed by 50 mg once daily (qd) (8 patients), MFG: 100 mg qd (8 patients) or MFG: 200 mg qd (8 patients). All agents will be given by slow IV infusion (MFG will be supplied by Astellas).
Sera - Blood samples will be collected at the end of the infusion (peak) and at 12 h and 24 h (trough) after the beginning of an infusion (day 3-4).
Each patients sera will be tested (MIC and cidal activity) against their own Candida isolate (if isolated). In addition, recent clinical isolates of C. glabrata will also be tested against patient sera (time-kill) to verify previous in vitro and animal PD studies (Cota. AAC. Nov. 2006; Wiederhold. AAC. May 2007).
Results:
Patient outcome, including Candida eradication, will be documented for each patient by repeat culture.
Serum concentrations (lab to be determined) and PK analysis of each echinocandin will be determined for each patient.
Serum cidal titers will be measured against each of the Candida isolates for each agent at each time period. Median and geometric mean Peak and duration of cidal activity will then be determined and compared.
6. Conditions and Keywords
Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Candidemia
Keywords
candidemia, echinocandin, micafungin, caspofungin
7. Study Design
Primary Purpose
Treatment
Study Phase
Phase 4
Interventional Study Model
Parallel Assignment
Masking
None (Open Label)
Allocation
Randomized
Enrollment
21 (Actual)
8. Arms, Groups, and Interventions
Arm Title
micafungin 100
Arm Type
Active Comparator
Arm Description
Patients receive Micafungin 100 mg qd
Arm Title
micafungin 200
Arm Type
Active Comparator
Arm Description
Patients receive 200 mg Micafungin qd
Arm Title
Caspofungin
Arm Type
Active Comparator
Arm Description
Patients receive caspofungin 70 mg LD followed by 50 mg qd
Intervention Type
Drug
Intervention Name(s)
micafungin
Other Intervention Name(s)
Micamine
Intervention Description
100 mg qd by slow IV infusion for 24 h
Intervention Type
Drug
Intervention Name(s)
Micafungin
Other Intervention Name(s)
Micamine
Intervention Description
200 mg qd by slow IV infusion for 24 h
Intervention Type
Drug
Intervention Name(s)
Caspofungin
Other Intervention Name(s)
Cancidas
Intervention Description
70 mg LD followed by 50 mg qd by slow IV infusion for 24 h
Primary Outcome Measure Information:
Title
Serum Cidal Activity as Tested Against Various Candida Isolates and Reported as Ex-vivo Effect (Log Inhibition of Growth)
Description
Serum cidal activity of serum collected at different timepoints from the patients will be tested against various Candida isolates and the ex-vivo effect reported as log inhibition (logrithmic measurement of the decrease in microbiological growth).
These Candida isolates had a range of minimum inhibitory concentrations (MIC) to Caspofungin (C) and Micafungin (M).
Time Frame
Pre-treatment, 1.5 hour (h), 12 h and 24 h after receiving the drug
10. Eligibility
Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria:
Adult patients with presumptive candidemia
Exclusion Criteria:
Patients with severe neutropenia (<500)
Patients with APACHE II scores > 20
Patients with severe liver disease
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Gary E Stein, Pharm.D.
Organizational Affiliation
Michigan State University
Official's Role
Principal Investigator
Facility Information:
Facility Name
Sparrow Hospital
City
Lansing
State/Province
Michigan
ZIP/Postal Code
48912
Country
United States
12. IPD Sharing Statement
Learn more about this trial
Comparison of Candida Eradication and Serum Cidal Activity of Echinocandins
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