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A Study in Healthy Volunteers to Assess Immune Response to Multiple Injections of Filgrastim Hospira or Neupogen Reference Product.

Last updated on May 9, 2018

FOR MORE INFORMATION
Study Location
SeaView Research, Inc.
Coral Gables, Florida, 33134 United States
Contact
1-800-718-1021
Eligibility criteria
Condition
The disease, disorder, syndrome, illness, or injury that is being studied.
Healthy Volunteers
Sex
Females and Males
Age
Pediatric Trials: 0-17 Years
Adult Trials: 18+ Years
18-65 years
Inclusion criteria
The factors, or reasons, that allow a person to participate in a clinical study.
Show details

1. Evidence of a personally signed and dated informed consent document indicating that
the subject has been informed of all pertinent aspects of the study.

2. Willing and able to comply with scheduled visits, treatment plan, laboratory tests,
and other study procedures.

3. Healthy male or female volunteers between 18 and 65 years of age (both inclusive).

4. Body mass index (BMI) between 19 and 30 kg/m2, inclusive, and body weight of not kg or >95 kg.

5. Subjects have abstained from the use of tobacco- or nicotine-containing products for
at least 90 days prior to dosing and have a negative urine screen for cotinine at
Screening.

6. Agrees to abstain from alcohol consumption for at least 48 hours prior to Day 1 of
dosing in each study period and throughout the 5 days of study treatment and has a
negative urine screen for alcohol at Screening.

7. Female subjects of non-childbearing potential must meet at least 1 of the following
criteria:

1. Achieved postmenopausal status, defined as follows: cessation of regular menses
for at least 12 consecutive months with no alternative pathological or
physiological cause; status will be confirmed by having a serum
follicle-stimulating hormone (FSH) level confirming the postmenopausal state;

2. Have undergone a documented hysterectomy and/or bilateral oophorectomy;

3. Have medically confirmed ovarian failure. All other female subjects (including
female subjects with tubal ligations) are considered to be of childbearing
potential

Exclusion criteria
The factors, or reasons, that prevent a person from participating in a clinical study.
Show details

Subjects with any of the following characteristics/conditions will not be included in the
study:

1. Investigator site staff members directly involved in the conduct of the study and
their family members, site staff members otherwise supervised by the investigator, or
subjects who are Pfizer employees, including their family members, directly involved
in the conduct of the study.

2. Participation in other studies involving an investigational drug within 30 days (or as
determined by the local requirement) or 5 half-lives preceding the first dose of
investigational product (whichever is longer) prior to study entry and/or during study
participation.

3. Acute or chronic medical or psychiatric condition including recent (within the past
year) or active suicidal ideation or behavior or laboratory abnormality that may
increase the risk associated with study participation or investigational product
administration or may interfere with the interpretation of study results and, in the
judgment of the investigator, would make the subject inappropriate for entry into this
study.

4. Any active systemic or immunologic disease or condition, including but not limited to
the following general categories: cardiovascular/pulmonary, hepatorenal, or systemic
infection, or lactation.

5. History of malignancy or current malignancy with the exception of adequately treated
squamous or basal cell carcinoma of the skin or cervical carcinoma in situ within 5
years.

6. Any disease or condition that might interfere with the absorption, distribution,
metabolism, or excretion of the study drug or would place the subject at increased
risk.

7. Hematologic laboratory abnormalities including leukocytosis (defined as total
leukocytes >11,000/mcL), leukopenia (defined as total leukocytes neutropenia (defined as absolute neutrophil count [ANC] thrombocytopenia (defined as platelet count of

8. Lacks adequate hepatic reserve as defined by aspartate aminotransferase (AST) and
alanine aminotransferase (ALT) ? 1.5 x the upper limit of normal (ULN) of the
reference lab; lack of renal reserve as defined by serum creatinine of ?1.2 x ULN for
reference lab or estimated glomerular filtration rate (eGFR) of ? 80 mg/min; or has
known history of glomerulonephritis.

9. Clinically significant, as judged by the investigator, vital sign, or 12-lead
electrocardiogram (ECG) abnormality.

10. History of biological growth factor exposure, including but not limited to filgrastim
and other G-CSFs in the context of treatment, prophylaxis, peripheral blood stem cell
mobilization, or previous investigational study setting.

11. Receipt of live vaccination, or exposure to communicable viral diseases such as
chicken pox, varicella, or measles within the 4 weeks prior to Screening.

12. Surgery within the 4 months prior to Screening.

13. Use of any prescription medicine (with the exception of contraceptives) within 7 days
or at least 5 half-lives, whichever is longer. Use of oral or parenteral anticoagulant
or antiplatelet agents and corticosteroids should be specifically queried.

14. Administration of a drug by depot injection (with exception of depot contraception)
within 30 days prior to the initial study drug administration or 5 half-lives of that
drug, whichever is longer.

15. Use of over the counter medications, including aspirin and non-steroidal
anti-inflammatory drugs, or natural preparations (dietary supplement or herbal
product) within 7 days or at least 5 half-lives, whichever is longer. Vitamins and
calcium supplements are allowed (not to exceed 100% daily value).

16. History of drug or alcohol abuse within 2 years prior to randomization, as determined
by the investigator or a positive urine screen for drugs of abuse at Screening.
Screening for drugs of abuse will minimally include cannabinoids, opiates,
barbiturates, amphetamines, cocaine, and benzodiazepines.

17. Drug sensitivity, allergic reaction to, or known hypersensitivity/idiosyncratic
reaction to E. coli-derived proteins, filgrastim, pegfilgrastim, other G-CSFs or any
component of the product: subjects with the rare heredity problem of fructose
intolerance are excluded due to the excipient sorbitol.

18. History of splenic rupture (or subject who is asplenic), pulmonary infiltrate or
pneumonia, sickle cell disorders, chronic neutropenia, thrombocytopenia, or
vasculitis.

19. Any clinically significant, as determined by the investigator, abnormal laboratory
evaluations, including human immunodeficiency virus antibody (HIVAb), hepatitis B
virus surface antigen (HBsAg), hepatitis C virus antibody (HCVAb) and liver function
taken at Screening. Negative HIVAb status will be confirmed at Screening and the
results will be maintained confidentially by the study site.

20. Blood donation (including plasma donations) of approximately 1 pint (500 mL) or more
within 60 days prior to dosing OR had a transfusion of any blood product within 90
days prior to Screening.

21. Pregnant female subjects, breastfeeding female subjects, fertile male subjects and
female subjects of childbearing potential who are unwilling or unable to use at least
1 highly effective method of contraception as outlined in the protocol for the
duration of the study and for at least 28 days after the last dose of investigational
product.

22. Unwilling or unable to comply with the criteria in the Lifestyle Requirements section
of the protocol.

NCT02923791
Pfizer
Completed
A Study in Healthy Volunteers to Assess Immune Response to Multiple Injections of Filgrastim Hospira or Neupogen Reference Product.

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A Study in Healthy Volunteers to Assess Immune Response to Multiple Injections of Filgrastim Hospira or Neupogen Reference Product.
A Phase I, Randomized Open-label, 2-period, Parallel Arm Study To Assess The Immunogenicity Of Multiple Subcutaneous (SC) Doses Of "Filgrastim Hospira" (US) Or US-approved Neupogen(Registered) Reference Product In Healthy Volunteers
This study compares the potential immunogenicity of two filgrastims, the proposed biosimilar Filgrastim Hospira (US) and the US-approved Neupogen reference product. Subjects will receive doses of one of the two filgrastims by injection of 5 micrograms/kilogram (mcg/kg). Subjects will receive 5 consecutive daily doses in Period 1 (Days 1-5) and a single dose on Day 1 of Period 2. Pre-dose and serial post-dose assessments of immunogenicity will be conducted each of the two study periods. In addition, safety assessments will be conducted throughout the study.
Not Provided
Interventional
Phase 1
Allocation: Randomized
Intervention Model: Parallel Assignment
Masking: None (Open Label)
Primary Purpose: Other
Healthy Volunteers
  • Biological: Filgrastim Hospira
    5 consecutive daily doses (Days 1-5) in Period 1 and 1 dose (Day 1) in Period 2.
    Other Name: Filgrastim
  • Biological: US-Approved Neupogen
    5 consecutive daily doses (Days 1-5) in Period 1 and 1 dose (Day 1) in Period 2.
    Other Name: Filgrastim
  • Experimental: Filgrastim Hospira
    Intervention: Biological: Filgrastim Hospira
  • Active Comparator: US-Approved Neupogen
    Intervention: Biological: US-Approved Neupogen
Not Provided


*   Includes publications given by the data provider as well as publications
identified by ClinicalTrials.gov Identifier (NCT Number) in Medline.
 
Completed
256
January 2017
January 2017   (Final data collection date for primary outcome measure)

Inclusion Criteria:

  1. Evidence of a personally signed and dated informed consent document indicating that the subject has been informed of all pertinent aspects of the study.
  2. Willing and able to comply with scheduled visits, treatment plan, laboratory tests, and other study procedures.
  3. Healthy male or female volunteers between 18 and 65 years of age (both inclusive).
  4. Body mass index (BMI) between 19 and 30 kg/m2, inclusive, and body weight of not < 50 kg or >95 kg.
  5. Subjects have abstained from the use of tobacco- or nicotine-containing products for at least 90 days prior to dosing and have a negative urine screen for cotinine at Screening.
  6. Agrees to abstain from alcohol consumption for at least 48 hours prior to Day 1 of dosing in each study period and throughout the 5 days of study treatment and has a negative urine screen for alcohol at Screening.
  7. Female subjects of non-childbearing potential must meet at least 1 of the following criteria:

    1. Achieved postmenopausal status, defined as follows: cessation of regular menses for at least 12 consecutive months with no alternative pathological or physiological cause; status will be confirmed by having a serum follicle-stimulating hormone (FSH) level confirming the postmenopausal state;
    2. Have undergone a documented hysterectomy and/or bilateral oophorectomy;
    3. Have medically confirmed ovarian failure. All other female subjects (including female subjects with tubal ligations) are considered to be of childbearing potential

Exclusion Criteria:

Subjects with any of the following characteristics/conditions will not be included in the study:

  1. Investigator site staff members directly involved in the conduct of the study and their family members, site staff members otherwise supervised by the investigator, or subjects who are Pfizer employees, including their family members, directly involved in the conduct of the study.
  2. Participation in other studies involving an investigational drug within 30 days (or as determined by the local requirement) or 5 half-lives preceding the first dose of investigational product (whichever is longer) prior to study entry and/or during study participation.
  3. Acute or chronic medical or psychiatric condition including recent (within the past year) or active suicidal ideation or behavior or laboratory abnormality that may increase the risk associated with study participation or investigational product administration or may interfere with the interpretation of study results and, in the judgment of the investigator, would make the subject inappropriate for entry into this study.
  4. Any active systemic or immunologic disease or condition, including but not limited to the following general categories: cardiovascular/pulmonary, hepatorenal, or systemic infection, or lactation.
  5. History of malignancy or current malignancy with the exception of adequately treated squamous or basal cell carcinoma of the skin or cervical carcinoma in situ within 5 years.
  6. Any disease or condition that might interfere with the absorption, distribution, metabolism, or excretion of the study drug or would place the subject at increased risk.
  7. Hematologic laboratory abnormalities including leukocytosis (defined as total leukocytes >11,000/mcL), leukopenia (defined as total leukocytes <4000/mcL), or neutropenia (defined as absolute neutrophil count [ANC] <1500/mcL), or thrombocytopenia (defined as platelet count of <150/mcL).
  8. Lacks adequate hepatic reserve as defined by aspartate aminotransferase (AST) and alanine aminotransferase (ALT) ? 1.5 x the upper limit of normal (ULN) of the reference lab; lack of renal reserve as defined by serum creatinine of ?1.2 x ULN for reference lab or estimated glomerular filtration rate (eGFR) of ? 80 mg/min; or has known history of glomerulonephritis.
  9. Clinically significant, as judged by the investigator, vital sign, or 12-lead electrocardiogram (ECG) abnormality.
  10. History of biological growth factor exposure, including but not limited to filgrastim and other G-CSFs in the context of treatment, prophylaxis, peripheral blood stem cell mobilization, or previous investigational study setting.
  11. Receipt of live vaccination, or exposure to communicable viral diseases such as chicken pox, varicella, or measles within the 4 weeks prior to Screening.
  12. Surgery within the 4 months prior to Screening.
  13. Use of any prescription medicine (with the exception of contraceptives) within 7 days or at least 5 half-lives, whichever is longer. Use of oral or parenteral anticoagulant or antiplatelet agents and corticosteroids should be specifically queried.
  14. Administration of a drug by depot injection (with exception of depot contraception) within 30 days prior to the initial study drug administration or 5 half-lives of that drug, whichever is longer.
  15. Use of over the counter medications, including aspirin and non-steroidal anti-inflammatory drugs, or natural preparations (dietary supplement or herbal product) within 7 days or at least 5 half-lives, whichever is longer. Vitamins and calcium supplements are allowed (not to exceed 100% daily value).
  16. History of drug or alcohol abuse within 2 years prior to randomization, as determined by the investigator or a positive urine screen for drugs of abuse at Screening. Screening for drugs of abuse will minimally include cannabinoids, opiates, barbiturates, amphetamines, cocaine, and benzodiazepines.
  17. Drug sensitivity, allergic reaction to, or known hypersensitivity/idiosyncratic reaction to E. coli-derived proteins, filgrastim, pegfilgrastim, other G-CSFs or any component of the product: subjects with the rare heredity problem of fructose intolerance are excluded due to the excipient sorbitol.
  18. History of splenic rupture (or subject who is asplenic), pulmonary infiltrate or pneumonia, sickle cell disorders, chronic neutropenia, thrombocytopenia, or vasculitis.
  19. Any clinically significant, as determined by the investigator, abnormal laboratory evaluations, including human immunodeficiency virus antibody (HIVAb), hepatitis B virus surface antigen (HBsAg), hepatitis C virus antibody (HCVAb) and liver function taken at Screening. Negative HIVAb status will be confirmed at Screening and the results will be maintained confidentially by the study site.
  20. Blood donation (including plasma donations) of approximately 1 pint (500 mL) or more within 60 days prior to dosing OR had a transfusion of any blood product within 90 days prior to Screening.
  21. Pregnant female subjects, breastfeeding female subjects, fertile male subjects and female subjects of childbearing potential who are unwilling or unable to use at least 1 highly effective method of contraception as outlined in the protocol for the duration of the study and for at least 28 days after the last dose of investigational product.
  22. Unwilling or unable to comply with the criteria in the Lifestyle Requirements section of the protocol.
Sexes Eligible for Study: All
18 Years to 65 Years   (Adult)
Yes
Contact information is only displayed when the study is recruiting subjects
United States
 
 
NCT02923791
C1121012
FILGRASTIM IMMUNOGENICITY US ( Other Identifier: Alias Study Number )
COMPARATIVE IMMUNOGENICITY ( Other Identifier: Alias Study Number )
No
Not Provided
Not Provided
Pfizer
Pfizer
Not Provided
Study Director: Pfizer CT.gov Call Center Pfizer
Pfizer
February 2017

ICMJE     Data element required by the

International Committee of Medical Journal Editors
and the
World Health Organization ICTRP

FOR MORE INFORMATION

Contact a representative by phone, email, or visiting thte study website. To get updates and notications about this trail, sign up using the form below.

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1-800-718-1021

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[email protected]



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