Pharmacokinetic/Pharmacodynamic (PK/PD) Study Evaluating Pegfilgrastim Hospira Compared to Neulasta (Amgen) in Healthy Volunteers

Hospira

Status and phase

Completed

Phase 1

Conditions

Healthy

Treatments

Drug: Pegfilgrastim Hospira

Drug: Neulasta (Amgen)

Study type

Interventional

Funder types

Industry

Identifiers

NCT00938678

PEG-09-01

EudraCT Number 2009-101433-42

Details and patient eligibility

About

This study compared the pharmacokinetics, pharmacodynamics and the safety of Pegfilgrastim Hospira and Neulasta® following a single dose of 6 mg of each product administered subcutaneously in Treatment Periods 1 and 2, respectively, in healthy volunteers.

Enrollment

71 patients

Sex

All

Ages

18 to 55 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

Healthy male or female subjects, 18-55 years inclusive.
Written informed consent given
Willing and able to comply with the requirements of the protocol and be available for the planned duration of the study.
Body Mass Index (BMI) between 19 and 30 kg/m2 inclusive and weight not <50 kg or >100 kg.
Female subjects who are using an effective method of contraception, or are surgically sterile.
Non-smokers or ex-smokers who have not smoked within the previous 12 months.

Exclusion criteria

Hypersensitivity to the Investigational medicinal product (IMP) or its constituents and/or hypersensitivity to E. Coli derived proteins, and/or previous exposure to the IMP.
History or presence of any clinically significant findings that, in the opinion of the Investigator, would preclude inclusion in the study.
History or presence of any clinically significant gastrointestinal pathology or symptoms, liver or kidney disease, or any other condition that might interfere with the absorption, distribution, metabolism or excretion of the drug.
Any clinically significant laboratory findings, including any ANC, platelet or haemoglobin result outside the reference range of the local laboratory.
Abnormal vital signs or abnormal 12-lead electrocardiogram (ECG) results, as judged by the Investigator to be clinically significant.
Females, pregnant or lactating, or planning to become pregnant during the time the subject is on study.
Subjects with a history of pulmonary infiltrate or pneumonia in the previous 6 months from the date of the screening visit.
Hereditary fructose intolerance.
Participation in any other clinical trial using a investigational product or device, within the previous 12 weeks from the date of the screening visit.
Positive result for human immunodeficiency virus (HIV) and/or hepatitis B and C tests.
Evidence of, or treatment for, drug or alcohol abuse within one year from date of screening visit.
Blood donation >=500 mL in the previous 12 weeks from the date of the screening visit.
Use of any prescription medication (excluding hormonal contraceptives) within 14 days prior to date of the screening visit.
Receipt of over-the-counter medicines which have not yet cleared from the body (five half-lives must have passed for the medicine to be considered to have cleared from the body). Vitamins, minerals and nutritional supplements may be taken at the discretion of the Investigator.