Study of the Effect of a 5-Day Regimen of Study Drug on Peripheral Stem Cell Mobilization in Healthy Participants

NCT ID: NCT03029000

Last Updated: 2022-12-13

Basic Information

• Recruitment Status: TERMINATED
• Clinical Phase: PHASE3
• Total Enrollment: 1 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2017-08-02
• Study Completion Date: 2017-10-30

Brief Summary

A multi-center, open-label, single-arm clinical study to assess effects of a 5-day regimen of 10 micrograms per kilogram (mcg/kg) of tbo-filgrastim administered subcutaneously daily on the mobilization of cluster of differentiation 34+ (CD34+) cells in at least 60 healthy male and female participants. The pharmacokinetics, pharmacodynamics, safety, tolerability, and immunogenicity of tbo-filgrastim will be assessed.

Conditions

Healthy Participants

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Tbo-filgrastim (GRANIX)

Participants will receive tbo-filgrastim 10 mcg/kg of body weight, subcutaneously on the morning of Days 1 to 5.

The actual dose of tbo-filgrastim administered to each, individual participant will be calculated at baseline according to his or her body weight and that specific dose (10 mcg/kg of body weight) for each, individual participant will remain the same for all consecutive daily doses.

If the collection goal will not meet after the first apheresis on Day 5, tbo-filgrastim 10 mcg/kg of body weight will be administered subcutaneously for up to 3 additional days (Days 6 to 8) followed by daily apheresis to reach the cumulative collection goal.

Group Type: EXPERIMENTAL

Tbo-filgrastim

Intervention Type: DRUG

solution for subcutaneous injection

Interventions

Tbo-filgrastim

solution for subcutaneous injection

Intervention Type: DRUG

Other Intervention Names

XM02

Eligibility Criteria

Inclusion Criteria

• Written informed consent is obtained from the participant
• The participant has a body weight of at least 50 kilograms (kg)
• The participant has a body mass index (BMI) of more than 18.5 and less than 35.0 kilograms per square meter (kg/m^2)
• The participant is in good health as determined by medical and psychiatric history, physical examination, electrocardiogram (ECG) recordings, serum chemistry, hematology, coagulation, urinalysis, and serology
• Women may be included only if they have a negative beta human chorionic gonadotropin (beta-hCG) test at baseline, are sterile (defined as documented hysterectomy, bilateral oophorectomy or bilateral salpingectomy, or congenitally sterile), or postmenopausal (defined as no menses for 12 months without alternative medical cause and increased follicle stimulating hormone [FSH] of above 35 units per liter [U/L] in women not using hormonal contraception or hormonal replacement therapy). Women of childbearing potential whose male partners are potentially fertile (that is, no vasectomy) must use highly effective birth control methods for the duration of the study and for 30 days after the last tbo-filgrastim administration
• The participant has a negative alcohol urine test and a negative urine drug screen
• The participant must be willing and able to comply with study restrictions
• The participant is human leukocyte antigen (HLA) -matched or haploidentical-related to the recipient

Exclusion Criteria

• The participant currently has or had a history of any clinically relevant gastrointestinal, hematologic, respiratory, psychiatric, renal, hepatic, cardiac, metabolic (such as, fructose intolerance), neurological, or any other disease or condition which may influence the physiological metabolic turnover (such as, severe endocrine diseases, febrile condition, severe infections), which may interfere with the study objectives, or which could expose the participant to undue risk through the participation in the clinical study
• The participant has had: (1) a trauma or surgery in the past 2 months; (2) a clinically relevant illness within 4 weeks before the first dose of tbo-filgrastim; (3) any acute illness within 1 week before the first dose of tbo-filgrastim; or (4) symptoms of any clinically relevant or acute illness at baseline
• The participant has existence or recent history of persistent pulmonary infiltrates, recent pneumonia, recent bronchitis, recurrent lung infections, or history or evidence of any lung disease including asthma, or current symptoms of upper respiratory tract infection. In the case of pneumonia, participant may be screened 12 weeks after cessation of antibiotic treatment
• The participant has findings of splenomegaly on sonography at screening, defined by length of spleen more than 12.3 centimeters (cm) and clinical judgment
• The participant has a history of malignancy, including hematologic malignancy, except for appropriately treated non-melanoma skin carcinoma in the last 5 years
• The participant has a clinically significant deviation from normal in ECG recordings or physical examination findings, as determined by the investigator
• The participant is pregnant or lactating, or was pregnant in the previous 6 months, or intends to get pregnant during the study or within 30 days after the last dose of study drug
• The participant has habitually consumed, within the last 2 years, more than 21 units of alcohol per week, or has a history or evidence of alcohol, narcotic, or any other substance abuse as defined by the Diagnostic and Statistical Manual of Mental Disorder, Fifth Edition (DSM-V, American Psychiatric Association 2013). Note: A unit of alcohol is equal to 1 ounce (29.6 milliliters [mL]) of hard liquor, 5 ounces (148 mL) of wine, or 8 ounces (236.8 mL) of beer
• The participant has taken any of the following investigational medicinal products (IMPs), medicinal products, or substances:

1. Any IMP within 30 days or 5 half-lives (whichever is longer) before the first dose of tbo-filgrastim, or in the case of a new chemical entity, 3 months or 5 half-lives (whichever is longer) before the first dose of tbo-filgrastim

2. Known history of treatment with blood-cell colony-stimulating factors

3. Current or recent (within 4 weeks) treatment with lithium

• The participant has donated plasma within 7 days before screening or has donated blood within 56 days before screening
• The participant has a documented or self-reported history of tuberculosis or recent travel to countries of endemic disease (last 8 weeks)
• The participant has 1 or more clinical laboratory test value(s) outside the range specified below, or any other clinically significant laboratory abnormality as determined by the investigator or medical monitor:

1. Hemoglobin less than or equal to (<=) 12.5 grams per deciliter (g/dL) (women) and hemoglobin <=13.5 g/dL (men)

2. Alanine aminotransferase (ALT) or aspartate aminotransferase (AST) values of greater than (>) 3 * the upper limit of the normal range (ULN)

3. Total bilirubin of >2 * ULN

4. Findings of cholestasis (eg, abnormal values of alkaline phosphatase)

• The participant has a positive test result for human immunodeficiency virus (HIV), hepatitis B surface antigen, antibodies to hepatitis C virus, immunoglobulin M (IgM) antibodies to cytomegalovirus, human T-lymphotropic virus, West Nile virus, malaria, or syphilis
• The participant has a documented or self-reported history of tuberculosis or recent travel to countries of endemic disease (last 8 weeks)
• The participant has, after resting for 5 minutes, increased blood pressure (BP) (defined as systolic BP in seated position of more than 145 millimeters of mercury [mm Hg] or diastolic BP in seated position of more than 95 mm Hg), or low BP (defined as systolic BP in seated position of less than 90 mm Hg or diastolic BP in seated position of less than 45 mm Hg) (Only 2 rechecks of the participant's BP are permitted for eligibility purposes)
• The participant has, after resting for 5 minutes, a pulse in seated position of less than 45 or more than 90 beats per minute (Only 2 rechecks of the participant's pulse are permitted for eligibility purposes)
• The participant is unwilling to refrain from vigorous exercise (eg, strenuous or unaccustomed weight lifting, running, bicycling) from 72 hours before Day 1 until Day 15
• The participant is unlikely to comply with the study protocol or is unsuitable for any other reasons, as judged by the investigator
• The participant has a history of autoimmune disease, including rheumatic diseases and thyroid disorders
• The participant has a history of deep vein thrombosis or pulmonary embolism
• The participant has thrombocytopenia defined as platelet count <150 * 109 cells per liter (cells/L) at screening or at baseline
• The participant has a history of bleeding problems (eg, hemophilia, thrombocytopenia, idiopathic thrombocytopenic purpura, clotting factor deficiencies or disorders)
• The participant has positive hemoglobin-solubility test
• The participant has a history of iritis or episcleritis
• The participant has a history of significant hypersensitivity, intolerance, or allergy to tbo-filgrastim or any other E. coli derived product or excipient, or other medicinal product, food, or substance, unless approved by the investigator

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

Teva Branded Pharmaceutical Products R&D, Inc.

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Teva Medical Expert, MD

Role: STUDY_DIRECTOR

Teva Branded Pharmaceutical Products R&D, Inc.

Locations

Teva Investigational Site 14029

Duarte, California, United States

Teva Investigational Site 14025

La Jolla, California, United States

Teva Investigational Site 14023

Beech Grove, Indiana, United States

Teva Investigational Site 14026

Detroit, Michigan, United States

Teva Investigational Site 14027

Chapel Hill, North Carolina, United States

Teva Investigational Site 14030

Cincinnati, Ohio, United States

Teva Investigational Site 14033

Greenville, South Carolina, United States

Teva Investigational Site 14035

Memphis, Tennessee, United States

Teva Investigational Site 14024

San Antonio, Texas, United States

Countries

United States

Provided Documents

Document Type: Study Protocol and Statistical Analysis Plan

View Document

Other Identifiers

TV44688-ONC-30054

Identifier Type: -

Identifier Source: org_study_id