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Pegfilgrastim PBPC Mobilization Study

Randomized, Double-Blind Study of Peripheral Blood Progenitor Cell (PBPC) Mobilization by Pegfilgrastim or Filgrastim for Autologous Transplantation in Subjects With Hodgkin's or Non-Hodgkin's Lymphoma.

Status
Completed
Phases
Phase 2
Study type
Interventional
Source
ClinicalTrials.gov
Registry ID
NCT00066092
Enrollment
41
Registered
2003-08-05
Start date
2003-04-30
Completion date
2004-10-31
Last updated
2008-02-28

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Hematology, Hodgkin's Lymphoma, Lymphoma, Non-Hodgkin's Lymphoma, Oncology

Keywords

PBPC transplant, Hodgkin's Disease, Non-Hodgkin's Lymphoma, NHL, mobilization

Brief summary

This is a randomized, double-blind, multi-center study to assess the safety and effectiveness of using a single subcutaneous (under the skin) injection of pegfilgrastim or daily subcutaneous injections of Filgrastim to mobilize stem cells for autologous transplantation in patients with Hodgkin's or non-Hodgkin's lymphoma.

Detailed description

This is a research study for Hodgkin's Disease and Non-Hodgkin's Lymphoma (NHL) patients who will receive high-dose chemotherapy with autologous peripheral blood stem cell (PBSC or PBPC) transplant. The chemotherapy doses are high enough to severely suppress the bone marrow (where blood cells are made) and cause very low blood counts. A collection of stem cells (very young blood cells) followed by reinfusion to restore blood counts will be done to stimulate recovery of your blood counts. This procedure is called leukapheresis. Giving growth factors to patients is a method to increase the number of PBPC that can be collected during leukapheresis. This process of giving growth factors to patients is called mobilization (moving cells from the bone marrow to the peripheral blood where they can be collected). The purpose of this study is to determine if pegfilgrastim, an investigational drug, can safely and effectively mobilize stem cells. Filgrastim (also known as NEUPOGEN® or G-CSF) is approved by the FDA for stem cell mobilization. Pegfilgrastim is a modified version of Filgrastim that is longer acting.

Interventions

DRUGpegfilgrastim 12 mg

Pegfilgrastim 12 mg given once for PBPC mobilization

DRUGfilgrastim

Filgrastim given daily for PBPC mobilization

DRUGpegfilgrastim 6 mg

Pegfilgrastim 6 mg given once for PBPC mobilization

Sponsors

Amgen
Lead SponsorINDUSTRY

Study design

Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
TRIPLE (Subject, Caregiver, Investigator)

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Hodgkin's or non-Hodgkin's lymphoma patients suitable for an autologous PBPC transplant - No previous bone marrow or PBPC transplant

Design outcomes

Primary

MeasureTime frame
CD34+ collection during the collection phase10 days

Secondary

MeasureTime frame
Time to ANC and platelet engraftment post-transplant100 days

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Feb 4, 2026