Pharmacokinetics of Anidulafungin (Ecalta ®) Intravenous Given to Patients at High Risk for Developing Invasive Fungal Disease (ANIDULAPK)

This study has been completed.
Sponsor:
Information provided by (Responsible Party):
Radboud University
ClinicalTrials.gov Identifier:
NCT01249820
First received: August 23, 2010
Last updated: January 31, 2013
Last verified: January 2013

August 23, 2010
January 31, 2013
November 2010
January 2013   (final data collection date for primary outcome measure)
pharmacokinetics [ Time Frame: two weeks per subject ] [ Designated as safety issue: No ]
comparison of pharmacokinetics of anidulafungin given once in every two days or once in every three days
Same as current
Complete list of historical versions of study NCT01249820 on ClinicalTrials.gov Archive Site
  • adequate exposure [ Time Frame: 2 weeks for each subject; analysis after 3 months after last subject inclusion ] [ Designated as safety issue: No ]
    To determine whether adequate exposure is attained by patients undergoing an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or receiving intensive chemotherapy for AML-MDS when using a q48 hour or a q72 hour dosing regimen
  • safety [ Time Frame: 3 weeks ] [ Designated as safety issue: Yes ]
    To determine the safety of anidulafungin in the patient population
Same as current
Not Provided
Not Provided
 
Pharmacokinetics of Anidulafungin (Ecalta ®) Intravenous Given to Patients at High Risk for Developing Invasive Fungal Disease
Pharmacokinetics of Anidulafungin Given Intravenously as Antifungal Prophylaxis to Recipients of an Allogeneic Haematopoietic Stem Cell Transplant Following Myeloablative Chemotherapy or Patients Receiving Intensive Chemotherapy for AML-MDS

The purpose of this study is to study the pharmacokinetics of anidulafungin (Ecalta ®) given intravenously as antifungal prophylaxis to recipients of an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or patients receiving intensive chemotherapy for AML-MDS who are at high risk for developing invasive fungal disease.

Alternate dosing strategies of echinocandin drugs might provide a better efficacy in the treatment of fungal infections as compared to the current label dosing strategy. Before conducting a controlled efficacy trial of echinocandins in haematology patients, the pharmacokinetics of these alternate dosing strategies need to be tested before bringing this idea to practice in a large randomised trial.

Therefore we want to conduct a pharmacokinetic study with anidulafungin given every 48 hours or every 72 hours. This research can be performed best in a group of patients at high risk for developing invasive fungal infections.

Recipients of an allogeneic haematopoietic stem cell transplant (HSCT) or patients receiving intensive chemotherapy for acute myeloid leukaemia (AML) or myelodysplastic syndrome (MDS) are at a relatively high risk of developing invasive fungal infections and are therefore candidates for primary prophylaxis. However, the options are limited to fluconazole which affords no protection against mould infections. Amphotericin B is not considered useful because of its desoxycholate formulation has too many side effects and its lipid formulations are too expensive nor have the broad-spectrum triazoles itraconazole and voriconazole proved their value in this setting. Anidulafungin is the first of a new class of antifungal drugs quite unlike any others attacking specifically the ß 1-3 -D-glucan synthase of the cell wall. It has relatively few side effects and appears safe and effective for treating Aspergillus and Candida infections. Since these two genera account for 90% of fungal infections in HSCT recipients the drug would seem an ideal candidate for prophylaxis.

Importantly, nothing is known about the pharmacokinetics of alternate dosing regimens of anidulafungin in this patient population. Therefore a pharmacokinetic study of a homogenous cohort of patients is necessary to test the assumption, that adequate exposure is obtained with alternate dosing and that it is safe.

Interventional
Phase 2
Allocation: Non-Randomized
Endpoint Classification: Pharmacokinetics Study
Intervention Model: Single Group Assignment
Masking: Open Label
  • Leukemia
  • Myelodysplastic Syndrome
  • Leukemia, Myeloid, Acute
  • Drug: anidulafungin 200 mg q48h
    Day 1-15: anidulafungin 200 mg q48h IV maintenance dose (8 dosages)
    Other Name: Ecalta
  • Drug: anidulafungin 300 mg q72h
    Day 1-13: anidulafungin 300 mg q72h IV maintenance dose (5 dosages)
    Other Name: Ecalta
  • Experimental: group A
    Day 1-15: anidulafungin 200 mg q48h IV maintenance dose (8 dosages)
    Intervention: Drug: anidulafungin 200 mg q48h
  • Experimental: group B
    Day 1-13: anidulafungin 300 mg q72h IV maintenance dose (5 dosages)
    Intervention: Drug: anidulafungin 300 mg q72h
Not Provided

*   Includes publications given by the data provider as well as publications identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
26
January 2013
January 2013   (final data collection date for primary outcome measure)

Inclusion Criteria:

  • Patient receives an allogeneic haematopoietic stem cell transplant following myeloablative chemotherapy or receives intensive chemotherapy for AML-MDS
  • Subject is at least 18 and not older than 65 years of age on the day of the first dosing
  • Has no signs or symptoms of invasive fungal disease
  • If a woman, is neither pregnant nor able to become pregnant and is not nursing an infant
  • Has an ALAT, ALAT, alkaline phosphatase < 5 times the upper limit of normal and a bilirubin level < 3 times the upper limit of normal
  • Is not known to be hypersensitive to echinocandin antifungal agents
  • Is managed with a quadruple central venous catheter (Arrow-Howes™ Quad-Lumen 8.5,5 French; Arrow International)
  • Subject is able and willing to sign the Informed Consent before screening evaluations

Exclusion Criteria:

  • Documented history of sensitivity to medicinal products or excipients similar to those found in the anidulafungin preparation
  • Known of Positive HIV test or hepatitis B or C test in history
  • History of QT time prolongation
  • History of or current abuse of drugs, alcohol or solvents
  • Inability to understand the nature of the trial and the procedures required
  • Has not previously participated in this trial
Both
18 Years to 64 Years
No
Contact information is only displayed when the study is recruiting subjects
Netherlands
 
NCT01249820
UMCN-AKF 10.01 / SC25
No
Radboud University
Radboud University
Not Provided
Principal Investigator: R Brüggemann, PharmD Radboud University
Radboud University
January 2013

ICMJE     Data element required by the International Committee of Medical Journal Editors and the World Health Organization ICTRP