Healthy Volunteers
Conditions
Keywords
Bioequivalence, Phase 1, Prefilled Pen, Prefilled syringe, pharmacokinetic, subcutaneous, hemophilia
Brief summary
The goal in this study is to show that there are not significant differences in biologic activity of the study drug when administered using either the prefilled pen and prefilled syringe.
Interventions
DRUGMarstacimab PFP
300 milligrams (mg) subcutaneous injection marstacimab PFP
DRUGMarstacimab PFS
300 mg subcutaneous injection of marstacimab PFS
Sponsors
Pfizer
Study design
Allocation
RANDOMIZED
Intervention model
CROSSOVER
Primary purpose
BASIC_SCIENCE
Masking
NONE
Eligibility
Sex/Gender
MALE
Age
18 Years to 55 Years
Healthy volunteers
Yes
Inclusion criteria
* Male participants who are overtly healthy as determined by medical evaluation * Participants who are willing and able to comply with all scheduled visits, treatment plan, laboratory tests, lifestyle considerations, and other study procedures. * BMI of 17.5 to 30.5 kg/m2; and a total body weight ≥ 50 kg (110 lb). * Capable of giving signed informed consent, which includes compliance with the requirements and restrictions listed in the ICD and in this protocol.
Exclusion criteria
* Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurological, dermatological, or allergic disease * Any condition possibly affecting drug absorption (eg, conditions affecting SC administration) * Previous or current treatment for and/or history of coronary artery diseases, venous or arterial thrombosis, or ischemic disease. * History of HIV infection, hepatitis B, or hepatitis C; positive testing for HIV, HBsAg, HBcAb or HCVAb * Other medical or psychiatric condition including recent (within the past year) or active suicidal ideation/behavior, laboratory abnormality or COVID-19 related condition that may increase the risk of study participation or, in the investigator's judgment, make the participant inappropriate for the study * Use of prescription or nonprescription drugs and dietary and herbal supplements within 7 days or 5 half-lives (whichever is longer) prior to the first dose of study intervention * Previous administration with an investigational drug within 30 days (or as determined by the local requirement) or 5 half-lives preceding the first dose of study intervention used in this study (whichever is longer). * A positive urine drug test at screening and/or admission * Screening supine BP ≥140 mm Hg (systolic) or ≥90 mm Hg (diastolic) * Baseline 12 lead ECG that demonstrates clinically relevant abnormalities that may affect participant safety or interpretation of study results * Participants with ANY of the following abnormalities in clinical laboratory tests at screening: * AST or ALT level ≥1.5 × ULN; * Total bilirubin level ≥1.5 × ULN. * An estimated glomerular filtration rate (eGFR) of \<60 mL/min/1.73m2 based on the CKD-EPI equation. * Resistance to activated protein C (or Factor V Leiden mutation), prothrombin 20210 mutation, antithrombin III deficiency, protein C deficiency, or protein S deficiency. * Presence of Lupus anticoagulant anti-cardiolipin antibodies (IgG, IgM or IgA) * High sensitivity C-reactive protein (hsCRP) above the upper limits of normal * Abnormal hematology values as defined by the following laboratory tests at Screening and/or admission: * Platelet count \<100,000/uL * Hemoglobin level \<10 g/dL * A positive COVID-19 test. * History of alcohol abuse or binge drinking and/or any other illicit drug use or dependence within 6 months of Screening * Use of tobacco/nicotine containing products in excess of the equivalent of 5 cigarettes/day * Blood donation (excluding plasma donations) of approximately 1 pint (500 mL) or more within 60 days prior to dosing. * Unwilling or unable to comply with the criteria in the Lifestyle Considerations section of the protocol * Investigator site staff or Pfizer employees directly involved in the conduct of the study, site staff otherwise supervised by the investigator, and their respective family members
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Area Under the plasma concentraiton time Curve from time zero extrapolated to infinite time (AUCinf) | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
| Maximum observed plasma concentration (Cmax) | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
Secondary
| Measure | Time frame |
|---|---|
| Apparent clearance after subcutaneous dose | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
| Apparent volume of distribution after subcutaneous dose | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
| Terminal half-life after subcutaneous dose | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
| Incidence of clinically significant laboratory value abnormalities | Baseline through the end of study, approximately 161 days |
| Area under the concentration time curve from time 0 to time of last quatifiable concenteration | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
| Incidence of Adverse Events | Baseline through the end of study, approximately 161 days |
| Incidence of neutralizing antibody against marstacimab | From Day 1, Period 1 through Day 21, Period 4 over a total of 84 days |
| Incidence of Serious Adverse Events | Baseline through the end of study, approximately 161 days |
| Incidence of anti-drug antibody against marstacimab | From Day 1, Period 1 through Day 21, Period 4 over a total of 84 days |
| Time for Cmax | Day 1 Hour 0, 1, 2, 4, 8, 12, 24, 48, 72; Day 7; Day 14; Day 21 after each dose |
Countries
Belgium
Outcome results
None listed