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Active Not RecruitingNCT03664830

Safety of Blood Stem Cell Mobilization With Plerixafor in Patients With Sickle Cell Disease

A Pilot Study To Evaluate The Safety And Feasibility of Hematopoietic Progenitor Cell Mobilization With Plerixafor as Part of a Gene Therapy Strategy in Sickle Cell Disease

Status
Active Not Recruiting
Phase
Phase 1
Study type
Interventional
Enrollment
5 (actual)
Sponsor
City of Hope Medical Center · Academic / Other
Sex
All
Age
18 Years – 40 Years
Healthy volunteers
Not accepted

Summary

The objective of this study is to investigate if up to two injections of plerixafor represent a safe and effective strategy to mobilize adequate numbers of CD34+ hematopoietic stem progenitor cells (HSPC) for autologous hematopoietic cell transplantation (HCT) in sickle cell disease (SCD) patients

Detailed description

Allogeneic hematopoietic cell transplantation (HCT) is the only curative option for sickle cell disease (SCD) patients but its use is significantly limited by the lack of compatible donors. Gene therapy using autologous hematopoietic stem cell (HSC) transplantation represents an alternative approach but requires the collection of significant numbers of cells. Severe adverse events have been observed in SCD patients after mobilization using the standard agent granulocyte colony-stimulating factor (G-CSF), and bone marrow harvesting is also associated with side effects. The use of a single administration of plerixafor has been suggested as an alternative mobilization strategy in SCD but may not mobilize sufficient number of HSC. In this study, our primary objective is to assess if up to two injections of plerixafor (starting dose level: 240 µg/kg/dose) are safe in SCD patients and can recruit enough blood stem cells needed for future gene therapy.

Conditions

Interventions

TypeNameDescription
DRUGPlerixaforUp to two subcutaneous injections of plerixafor (starting dose level: 240 µg/kg/dose)

Timeline

Start date
2018-09-19
Primary completion
2026-08-03
Completion
2026-08-03
First posted
2018-09-11
Last updated
2025-09-16

Locations

1 site across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT03664830. Inclusion in this directory is not an endorsement.