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Nebulized Liposomal Amphotericin B Ambisome for Prophylaxis of Invasive Pulmonary Aspergillosis (AMBINEB)

Primary Purpose

Acute Myeloid Leukemia, Allogeneic Haematopoietic Progenitor Cell Transplant

Status
Completed
Phase
Phase 2
Locations
Spain
Study Type
Interventional
Intervention
liposomal Amphotericine B
Sponsored by
PETHEMA Foundation
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional prevention trial for Acute Myeloid Leukemia focused on measuring Acute myeloid Leukemia, Allogeneic haematopoietic progenitor cell transplant, Acute Invasive Aspergillosis

Eligibility Criteria

18 Years - undefined (Adult, Older Adult)All SexesDoes not accept healthy volunteers

Inclusion Criteria:

  • Patient has decided voluntary to consent his or her participation signing the consent form before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to their future medical care.
  • Patients with Acute myeloid Leukemia (AML), that will start induction chemotherapy or those patients submitted to an Allogeneic haematopoietic progenitor cell transplant.
  • The patient is >18 years old.

Exclusion Criteria:

  • Patient with prior Invasive Pulmonary Aspergillosis (IPA) history.
  • History of allergy or hypersensitivity to Amphotericin B.
  • Patient with intellectual deficit or patients with psychological alterations that make impossible the trial understanding.
  • Pregnancy or breastfeeding.
  • Patient has received other investigational drug or non traded product within 30 days before trial beginning.
  • Patient is enrolled in another clinical research study or/and is receiving an investigational agent for any reason.
  • Patient had major surgery within 4 weeks before enrollment.

Sites / Locations

  • Hospital de la Santa Creu i Sant Pau
  • Hospital Universitario de la Princesa
  • Hospital Universitario de Salamanca
  • Hospital Universitario la Fe

Arms of the Study

Arm 1

Arm Type

Experimental

Arm Label

1

Arm Description

AML patients in induction chemotherapy treatment will received prophylaxis with nebulized liposomal amphotericin B (24 mg/week). It will be maintained during the intensification chemotherapy and in periods between cycles. If patient required ALO-TPH, the prophylaxis should be followed.

Outcomes

Primary Outcome Measures

Efficacy and safety prophylaxis against IPA in LMA patients.

Secondary Outcome Measures

Full Information

First Posted
October 20, 2006
Last Updated
May 11, 2009
Sponsor
PETHEMA Foundation
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1. Study Identification

Unique Protocol Identification Number
NCT00391014
Brief Title
Nebulized Liposomal Amphotericin B Ambisome for Prophylaxis of Invasive Pulmonary Aspergillosis
Acronym
AMBINEB
Official Title
AMBINEB: Clinical Trial to Evaluate Tolerance and Safety of Nebulized Liposomal Amphotericin B Ambisome for Prophylaxis of Invasive Pulmonary Aspergillosis in Patients With Acute Myeloid Leukemia and Allogeneic Haematopoietic Progenitor Cell Transplant (Alo-HPCT)
Study Type
Interventional

2. Study Status

Record Verification Date
May 2009
Overall Recruitment Status
Completed
Study Start Date
January 2006 (undefined)
Primary Completion Date
December 2008 (Actual)
Study Completion Date
April 2009 (Actual)

3. Sponsor/Collaborators

Name of the Sponsor
PETHEMA Foundation

4. Oversight

Data Monitoring Committee
Yes

5. Study Description

Brief Summary
The trial is planned as a multicentric, national, phase II, open-label trial to evaluate safety and tolerance of nebulized Liposomal Amphotericin B (Ambisome) for LMA patients during the induction therapy ,intensification, plus Allogeneic Haematopoietic Progenitor Cell transplant in due course, as well for patients diagnosed of several malignant haematologic diseases and treated with Allogeneic Haematopoietic Progenitor Cell Transplant
Detailed Description
The invasive fungal infection (IFI) is the most common cause of mortality related to autologous stem cell transplant. Taking into account that Saprophytic Aspergillus is usually acquired by inhalation, to protect the bronchial tree just before the tissue invasion is quite attractive. In haematologic patients, as well as those ones subjected to an Allogeneic haematopoietic progenitor cell transplant, there is another group of patients at high risk of Invasive Pulmonary Aspergillosis (IPA). These are those patients with acute myeloid leucemia (AML), submitted to induction, intensification or consolidation polychemotherapy. The IPA incidence rate in these patients, whenever during their evolution, reaches 18-20%, with usual treatments. Furthermore, unlike allogeneic haematopoietic progenitor cell transplant patients, neutropenia was the only IPA risk factor. Nowadays, pharmacologic prophylaxis against IPA, in patients with allogeneic haematopoietic progenitor cell transplant and patients affected by AML in induction or intensification therapy is far from being optimal, because of problems related to tolerance and drug interactions . The Nebulized Liposomal Amphotericin B (Ambisome) prophylaxis against IPA has shown good tolerance, safety and efficacy in lung transplant recipients. Extrapolating the results obtained in lung transplant recipients, we get the conclusion that it would be essential to study safety and tolerance of nebulized AMBISOME in the group of patients with different peculiarities, mucositis secondary to chemotherapy, and high incidence of IPA in order to reach the goal of evaluate its efficacy as prophylaxis against IPA in this kind of patients

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Acute Myeloid Leukemia, Allogeneic Haematopoietic Progenitor Cell Transplant
Keywords
Acute myeloid Leukemia, Allogeneic haematopoietic progenitor cell transplant, Acute Invasive Aspergillosis

7. Study Design

Primary Purpose
Prevention
Study Phase
Phase 2
Interventional Study Model
Single Group Assignment
Masking
None (Open Label)
Allocation
Non-Randomized
Enrollment
150 (Anticipated)

8. Arms, Groups, and Interventions

Arm Title
1
Arm Type
Experimental
Arm Description
AML patients in induction chemotherapy treatment will received prophylaxis with nebulized liposomal amphotericin B (24 mg/week). It will be maintained during the intensification chemotherapy and in periods between cycles. If patient required ALO-TPH, the prophylaxis should be followed.
Intervention Type
Drug
Intervention Name(s)
liposomal Amphotericine B
Intervention Description
AML patients in induction chemotherapy treatment will received prophylaxis with nebulized liposomal amphotericin B (24 mg/week). It will be maintained during the intensification chemotherapy and in periods between cycles. If patient required ALO-TPH, the prophylaxis should be followed.
Primary Outcome Measure Information:
Title
Efficacy and safety prophylaxis against IPA in LMA patients.
Time Frame
1 year

10. Eligibility

Sex
All
Minimum Age & Unit of Time
18 Years
Accepts Healthy Volunteers
No
Eligibility Criteria
Inclusion Criteria: Patient has decided voluntary to consent his or her participation signing the consent form before performance of any study-related procedure not part of normal medical care, with the understanding that consent may be withdrawn by the patient at any time without prejudice to their future medical care. Patients with Acute myeloid Leukemia (AML), that will start induction chemotherapy or those patients submitted to an Allogeneic haematopoietic progenitor cell transplant. The patient is >18 years old. Exclusion Criteria: Patient with prior Invasive Pulmonary Aspergillosis (IPA) history. History of allergy or hypersensitivity to Amphotericin B. Patient with intellectual deficit or patients with psychological alterations that make impossible the trial understanding. Pregnancy or breastfeeding. Patient has received other investigational drug or non traded product within 30 days before trial beginning. Patient is enrolled in another clinical research study or/and is receiving an investigational agent for any reason. Patient had major surgery within 4 weeks before enrollment.
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Ruiz Isabel, Dr
Organizational Affiliation
Hospital Vall d'Hebron
Official's Role
Principal Investigator
First Name & Middle Initial & Last Name & Degree
Rovira Montserrat, Dr
Organizational Affiliation
Hospital Clinic of Barcelona
Official's Role
Principal Investigator
Facility Information:
Facility Name
Hospital de la Santa Creu i Sant Pau
City
Barcelona
Country
Spain
Facility Name
Hospital Universitario de la Princesa
City
Madrid
Country
Spain
Facility Name
Hospital Universitario de Salamanca
City
Salamanca
Country
Spain
Facility Name
Hospital Universitario la Fe
City
Valencia
Country
Spain

12. IPD Sharing Statement

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Links:
URL
http://www.aehh.org
Description
Spanish association of Haematology

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Nebulized Liposomal Amphotericin B Ambisome for Prophylaxis of Invasive Pulmonary Aspergillosis

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