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Completed

NCT Number: NCT03993639

KRN125 for Mobilization of Hematopoietic Stem Cells

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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Key information

Age range

20 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Hokkaido University Hospital

Sapporo, Hokkaido, Japan

About this study

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.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Japanese subjects aged 20 to 55 years or younger at the submission of the written informed consent form
  • Women weighing 40 kg or more and 80 kg or less and men weighing 45 kg or more and 80 kg or less at the time of the preliminary examination

Exclusion criteria

  • Subjects with a current medical history or who have been judged to be inappropriate for the study (e.g., significant neurological, hepatic, renal, endocrine, cardiovascular, blood, gastrointestinal, respiratory, and metabolic diseases, malignancies, myeloproliferative disorder, or psychiatric disorders)
  • Individuals with alcohol or drug dependence, or individuals who have not tested negative for all drugs of abuse in the preliminary test
  • Subjects with a history or current history of drug allergy or symptomatic allergy
  • .Active infection or history of recurrent infection- However, only patients who are HBsantibody-positive by hepatitis B vaccination and whose HBV-DNA is less than the lower limit of quantitation will be allowed to participate in this study.
  • Subjects who used drugs within 2 weeks before administration of the investigational drug.
  • Subjects who have had at least 200 mL of blood drawn within 3 months before administration of the investigational drug.
  • Pregnant or lactating

Treatment and study plan

pegfilgrastim

Drug

Single dose of SC administration

Primary outcomes

  1. Achievement of >20 cells/μL positive for CD34 in peripheral blood from baseline to Day 7

    Time frame: Baseline to Day 7

Secondary outcomes

  1. • Period from baseline to first time peripheral blood CD34 positive cells >20 cells/μL

    Time frame: Baseline to Day 15 or through study completion, an average of 1 year

  2. • Time from baseline to peak peripheral blood CD34 positive cells

    Time frame: Baseline to Day 15 or through study completion, an average of 1 year

  3. • Achievement of >10 cells/μL positive for CD34 in peripheral blood from baseline to Day 7

    Time frame: Baseline to Day 7

  4. • Peripheral blood CD34 positive cell count

    Time frame: Baseline to Day 15 or through study completion, an average of 1 year

  5. • Peripheral blood white blood cell count

    Time frame: Baseline to Day 15 or through study completion, an average of 1 year

  6. • Peripheral blood neutrophil count

    Time frame: Baseline to Day 15 or through study completion, an average of 1 year

Sponsors and collaborators

Lead sponsor

Kyowa Kirin Co., Ltd.

Industry

Registry information

Official study title

A Phase II Clinical Trial of KRN125 to Mobilize Hematopoietic Stem Cells Into Peripheral Blood in Healthy Volunteers

Important dates

Study start
2019
Primary completion
2020
Study completion
2020
First posted
Jun 21, 2019
Registry last updated
Jan 22, 2021

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

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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