Status:
COMPLETED
Biosimilarity Study of Subcutaneous Pegfilgrastim in Healthy Volunteers
Lead Sponsor:
Megalabs
Conditions:
Neutropenia
Eligibility:
MALE
18-55 years
Phase:
PHASE1
Brief Summary
This study will compare the pharmacokinetics and pharmacodynamics, after single subcutaneous application, in healthy men, between pegfilgrastim formulation, produced by Megalabs (test product) and Neu...
Eligibility Criteria
Inclusion
- Healthy eligible participants able to read, understand and sign the latest version of the Informed Consent Form (ICF) approved by the Research Ethics Committee (CEP)
- Males aged between 18 and 55 years
- Be characterized as a healthy research participant, based on medical history general physical examination and vital signs, laboratory tests and electrocardiogram (ECG),
- Not indicating any evidence of disease
- Body weight between 60-100 kg;
- Body Mass Index (BMI) ≥ 18.5 and ≤ 29.9 Kg / m2;
- Negative test for coronavirus
Exclusion
- Present one or more flu-like symptoms such as: fever (body temperature greater than or equal to 37.8 ° C), cough, dyspnoea, myalgia and fatigue, respiratory symptoms, gastrointestinal symptoms (such as diarrhea) within 7 days prior to the hospitalization period (all periods);
- Direct and significant medical contact with people who tested positive for coronavirus testing within 14 days prior to the hospitalization period (all periods);
- Living in the same household as people who are in the risk group with the worst prognosis for coronavirus infection, such as individuals over 60, individuals with respiratory problems, immunosuppressed or those with chronic diseases, such as heart or diabetes (all periods).
- Participants diagnosed with malignant disease in the last 5 years, with the exception of successfully treated basal cell carcinoma;
- Participants with a previous diagnosis of severe asthma, sickle cell anemia, idiopathic urticaria or anaphylaxis;
- Participants with chronic diseases and, therefore, who regularly use medications;
- Being a smoker or quitting less than 6 months ago;
- Participants who consume more than 5 cups of tea or coffee a day and who cannot abstain during the trial period;
- History of alcohol and illicit drug abuse
- Electrocardiogram (ECG) findings that, at the investigator's discretion, may compromise participation in the trial;
- History or presence of gastrointestinal or liver diseases or any other condition that interferes with the absorption, distribution, excretion or metabolism of the drug;
- Use of lithium 2 weeks before and / or after medication administration;
- Participants who are hypersensitive or contraindicated to use any of the components of the formulation;
- Research participants who have participated in clinical trial protocols in the last 12 (twelve) months (Resolution CNS 251, of August 7, 1997, item III, subitem J);
- Have donated blood (\> 500 mL) or have undergone major surgery in the 3 (three) months preceding the date of signing the informed consent form;
- Have received any vaccine in the 3 (three) months preceding the date of signing the informed consent form;
Key Trial Info
Start Date :
March 18 2022
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
September 18 2022
Estimated Enrollment :
72 Patients enrolled
Trial Details
Trial ID
NCT04873765
Start Date
March 18 2022
End Date
September 18 2022
Last Update
August 16 2024
Active Locations (1)
Enter a location and click search to find clinical trials sorted by distance.
1
Marcos Giusti
Montevideo, Uruguay, 11300