Clinical Trials Directory

Trials / Completed

CompletedNCT01413568

Safety and Efficacy of POL6326 for Mobilization/Transplant of Sibling Donor in Patients With Hematologic Malignancies

A Phase I/II Study Evaluating the Safety and Efficacy of Intravenous POL6326 for the Mobilization and Transplantation of HLA-Matched Sibling Donor Hematopoietic Stem Cells in Patients With Advanced Hematological Malignancies

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
38 (actual)
Sponsor
Polyphor Ltd. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Not accepted

Summary

Determine the safety and tolerability of POL6326 when used as a single mobilization agent.

Detailed description

Current protocols use G-CSF to mobilize hematopoietic progenitor cells from matched sibling donors. This process requires from four to six days of G-CSF injection and is associated with significant morbidity, most notably bone pain. POL6326 is associated with few side effects and collection of cells occurs on the same day as POL6326 administration. This study will evaluate the safety and efficacy of this novel agent for hematopoietic progenitor cell mobilization and allogeneic transplantation based on the following hypotheses: 1. Donors mobilized with intravenous POL6326 will require fewer collections than have previously been seen for donors mobilized with subcutaneous plerixafor. 2. Healthy HLA-matched donors receiving one or two infusions of POL6326 will mobilize sufficient CD34+ cells (at least 2.0 x 106 CD34+ cells/kg recipient weights) following leukapheresis to support a hematopoietic cell transplant. 3. IV POL6326 will result in more rapid kinetics and a higher maximum (peak) of human CD34+ stem cells mobilized from human normal allogeneic donors compared to previous donors who were mobilized with plerixafor. 4. The hematopoietic cells mobilized by IV POL6326 will be functional and will result in prompt and durable hematopoietic engraftment following transplantation into HLA-identical siblings with advanced hematological malignancies using various non-myeloablative and myeloablative conditioning regimens and regimens for routine GVHD prophylaxis.

Conditions

Interventions

TypeNameDescription
DRUGPOL6326
PROCEDURELeukapheresis
PROCEDUREPBSC Transplant

Timeline

Start date
2012-04-01
Primary completion
2015-11-01
Completion
2015-12-01
First posted
2011-08-10
Last updated
2016-02-26

Locations

2 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01413568. Inclusion in this directory is not an endorsement.