CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 150 target
Drug / intervention
liposomal Amphotericine Bdrug
Likely dose
liposomal Amphotericine B 24 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT00391014
NCT00391014Phase 2Completed

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)

PETHEMA Foundation·interventional·Posted Oct 23, 2006·Updated May 12, 2009

In Brief

A Phase 2 clinical trial evaluating liposomal Amphotericine B for Acute Myeloid Leukemia and Allogeneic Haematopoietic Progenitor Cell Transplant. Completed, enrolled 150 participants across 4 sites.

Detailed 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

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesSpain
Collaborators--

Timeline

Phase 2CompletedFinished
2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
First PostedOct 23, 2006
Enrollment StartJan 1, 2006
Primary CompletionDec 1, 2008
Study CompletionApr 1, 2009
TodayJul 2, 2026
Enrollment to primary: 2.9 yearsPosted 19.7 years ago

Interventions

liposomal Amphotericine Bdrug

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.