Hokkaido University Hospital
Sapporo, Hokkaido, Japan
NCT Number: NCT03993639
Data collection to evaluate safety and effect of hematopoietic stem cell mobilization into the peripheral blood after a single subcutaneous (SC) dose of KRN125(Pegfilgrastim)in healthy adults.
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Notify Me20 year–55 year
All sexes
Interventional
Phase 2
Sapporo, Hokkaido, Japan
KRN125 is administered as a single SC dose to the Day 1. The stem cell mobilization protocols will be monitored for safety and efficacy during the mobilization period.
Healthy volunteers accepted: Yes
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Single dose of SC administration
Time frame: Baseline to Day 7
Time frame: Baseline to Day 15 or through study completion, an average of 1 year
Time frame: Baseline to Day 15 or through study completion, an average of 1 year
Time frame: Baseline to Day 7
Time frame: Baseline to Day 15 or through study completion, an average of 1 year
Time frame: Baseline to Day 15 or through study completion, an average of 1 year
Time frame: Baseline to Day 15 or through study completion, an average of 1 year
Kyowa Kirin Co., Ltd.
Industry
A Phase II Clinical Trial of KRN125 to Mobilize Hematopoietic Stem Cells Into Peripheral Blood in Healthy Volunteers
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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