← Eichor
Study identifier: NCT07692841 Synced from ClinicalTrials.gov · July 29, 2026
● Recruiting

Single-Dose vs. Divided-Dose G-CSF for Stem Cell Mobilization in Healthy Allogeneic Donors

Condition: Healthy Hematopoietic Stem Cell Donor · Healthy Allogeneic Hematopoietic Stem Cell Donor  ·  Sponsor: First Affiliated Hospital of Zhejiang University

PhasePhase 3
Planned participants560
Who can joinAll sexes, 18 Years to 65 Years
Healthy volunteersNo

About this study

National and international guidelines/consensus recommend G-CSF (granulocyte colony-stimulating factor) at 10 μg/kg/day as a single daily dose or divided into two daily doses for mobilization in healthy donors for allogeneic hematopoietic stem cell transplantation. However, there is no consensus or standard regarding single versus divided dosing, and high-quality evidence is lacking. Existing randomized controlled trials have small sample sizes and inconsistent conclusions, and none have focused on Asian population characteristics (e.g., body weight and drug metabolism differences). This study aims to provide level I evidence to optimize donor experience and define the optimal administration strategy. Inclusion criteria: Healthy allogeneic stem cell donors aged 18-60 years, meeting institutional standard donor screening criteria (HLA matching, normal blood counts, normal liver and kidney function, negative infection screening), and providing written informed consent. Primary endpoint: The rate of achieving a first apheresis yield of ≥ 4 × 10⁶ CD34⁺ cells/kg (donor body weight) after 5 days of G-CSF mobilization. Secondary endpoints: The rate of achieving ≥ 2 × 10⁶ CD34⁺ cells/kg with at most one apheresis; time to myeloid, platelet, and erythroid engraftment in recipients; the proportion and composition of immune cells (CD34⁺, CD3⁺, CD19⁺, CD56⁺, etc.) in the apheresis product; donor adverse events; donor-reported outcomes; and the difference in CD34⁺ stem cell yields betw…

This description comes directly from the study's public registry record.

Talk to the study team

YIBO Wu  ·  +8657187233801  ·  wuyibo7@126.com

Always discuss trial participation with your own doctor first.

Locations (8)

Xiangya Hospital of Central South UniversityChangsha, Hunan, ChinaRecruiting
Sir Run Run Shaw Hospital, Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting
The First Affiliated Hospital, Zhejiang University School of Medicine.Hangzhou, Zhejiang, ChinaRecruiting
The Second Affiliated Hospital of Zhejiang University School of MedicineHangzhou, Zhejiang, ChinaRecruiting
Jinhua Central HospitalJinhua, Zhejiang, ChinaRecruiting
The Affiliated People's Hospital of Ningbo UniversityNingbo, Zhejiang, ChinaRecruiting
The First Affiliated Hospital of Ningbo UniversityNingbo, Zhejiang, ChinaRecruiting
The First Affiliated Hospital of Wenzhou Medical UniversityWenzhou, Zhejiang, ChinaRecruiting

Follow this study

Get one email when the public record changes — results posted, or the study's status changes. Nothing else, ever.

We email about this public record only. Unsubscribe anytime with one click. Never medical advice.

Is this your study? This page was generated automatically from the public registry record. Sponsors can claim it — free — to add branding and verified contact routing. Claim this page →

This page is independently generated by Eichor from the public ClinicalTrials.gov record and re-synced daily. It is not the sponsor's official website unless claimed. Nothing here is medical advice; eligibility is always determined by the study team — talk to your own doctor first.

Source record: clinicaltrials.gov/study/NCT07692841