Study of Pharmacodynamic Equivalence of Enoxaparin Rovi to Clexane®, in Healthy Volunteers
NCT ID: NCT03363477
Last Updated: 2017-12-06
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
46 participants
INTERVENTIONAL
2015-09-25
2015-12-01
Brief Summary
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As secondary objective, to evaluate the safety and tolerability of enoxaparin Rovi (100 mg/mL) in healthy volunteers.
Detailed Description
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On Day 1 of Period 1, subjects will receive a single dose by subcutaneous route of the assigned study drug: enoxaparin (100 mg/mL) 100-mg SC injection manufactured by Rovi Spain, or Clexane (100 mg/mL) 100-mg SC injection manufactured by Sanofi EU; after an overnight fasting period of at least 10 hours. Subjects will continue fasting for at least 4 hours after study drug administration.
The washout period between administrations of study drug in each period will be at least 7 days.
On Day 1 of Period 2, subjects will cross over to receive the dose of the other drug, after an overnight fasting period of at least 10 hours. The total duration of the study will be approximately 6 weeks.
Conditions
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Keywords
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Study Design
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RANDOMIZED
CROSSOVER
TREATMENT
TRIPLE
Study Groups
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AB treatment sequence
Period 1-Test Treatment A: enoxaparin (100 mg/mL) 100-mg SC injection, manufactured by Rovi (Spain) Period 2-Reference Treatment B: Clexane (100 mg/mL) 100-mg SC injection, manufactured by Sanofi (EU)
Enoxaparin
Clexane
BA treatment sequence
Period 1-Reference Treatment B: Clexane (100 mg/mL) 100-mg SC injection, manufactured by Sanofi (EU) Period 2-Test Treatment A: enoxaparin (100 mg/mL) 100-mg SC injection, manufactured by Rovi (Spain)
Enoxaparin
Clexane
Interventions
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Enoxaparin
Clexane
Other Intervention Names
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Eligibility Criteria
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Inclusion Criteria
2. Subject is between the ages of 18 and 45 years, inclusive.
3. All female subjects must have a negative pregnancy test at Screening and upon check-in to the clinic.
4. Women of childbearing potential must use or have used one of the following acceptable birth control methods: Surgical sterilization (bilateral tubal ligation, hysterectomy, bilateral oophorectomy) for at least 6 months before the first dose of study drug;Intrauterine device in place for at least 3 months before the first dose of study drug; or barrier method (condom, diaphragm) for at least 21 days before the first dose of study drug and throughout the study.
5. Subject has a body mass index between 18 and 30 kg/m2, inclusive.
6. Subject is able and willing to abstain from alcohol from 48 hours before the first dose of study drug through the end of the study.
7. Subject has no clinically significant abnormalities in medical history, vital sign measurements, or physical examination findings.
8. Subject has computerized 12-lead electrocardiogram (ECG) results showing no signs of clinically relevant pathology or deviations, as judged by the investigator.
9. Subject has hematology, serum chemistry, coagulation, and urinalysis test results within the reference ranges (Hb ≥7.5 mmol/L and ≥8.5 mmol/L for female and male, respectively) or showing no clinically relevant deviations, as judged by the investigator. Thrombocytes at screening have to be within the normal range.
10. Subject is a nonsmoker or has quit smoking at least 6 months before the first dose of study drug.
Exclusion Criteria
1. Subject has active or recurring clinically significant skin, head, ears, eyes, nose, throat, respiratory, cardiovascular, gastrointestinal, endocrine/metabolic, genitourinary, neurologic, hematologic, musculoskeletal, immunologic, allergic, psychological/psychiatric, or other disease requiring medical treatment.
2. Female subject with weight \< 45 kg or male subject with weight \< 57 kg.
3. Subject is a woman who is pregnant or breastfeeding.
4. Subject has systolic blood pressure greater than 150 mm Hg or diastolic blood pressure greater than 90 mm Hg at Screening (confirmed upon repeat measurement).
5. Subject has a calculated (Cockroft \& Gault formula) creatinine clearance less than 80 mL/minute and the value does not return to within reference range upon retest.
6. Subject has Hb \<7.5 mmol/L and \<8.5 mmol/L for female and male, respectively.
7. Subject has an active malignancy of any type other than nonmelanomatous skin malignancies.
8. Subject has any history of alcohol abuse or drug addiction.
9. Subject has any history of relevant drug and/or food allergies.
10. Subject has used an investigational drug within 60 days before the first dose of study drug.
11. Subject has used any prescription drugs (with special attention to antiplatelet or anticoagulant medication, eg, acetyl salicylic acid, NSADs, clopidogrel, warfarin, acenocumarol, heparin, low molecular weight heparin, dabigatran, rivaroxaban, apixaban) or over-the-counter medication that may affect coagulation (including aspirin or NSAIDs) within 4 weeks before dosing, or any other over-the-counter medication (including vitamins, herbal supplements, or dietary supplements) within 2 weeks before dosing.
12. Subject has donated or lost 550 mL or more of blood (including plasmapheresis) within 60 days before the first dose of study drug.
13. Subject has a positive test result for drugs of abuse (opiates, methadone, cocaine, amphetamines, cannabinoids, barbiturates, benzodiazepines, tricyclic antidepressants, oxycodone), cotinine, or alcohol.
14. Subject has a positive test result for human immunodeficiency virus (1 or 2) antibody, hepatitis B surface antigen, or hepatitis C virus antibody.
15. Subject has any illness within 5 days before the first dose of study drug.
16. Subject has a positive test for fecal occult blood at Screening.
17. Subject has any history and/or current conditions of bleeding tendency such as: active bleeding, known bleeding diathesis or hemostatic defects due to severe hepatic or renal disease; recent gastrointestinal or genitourinary bleeding (10 days before study entry) women of child-bearing potential with normal cyclic bleeding which is not considered as heavy menstruation by the investigator, are allowed for inclusion; diabetic hemorrhagic retinopathy, or other hemorrhagic ophthalmic conditions.
18. Subject has a known history or family history of any relevant congenital or acquired coagulation disorder (eg, hemophilia, von Willebrand-Jürgens syndrome, or activated protein C resistance based upon Factor V Leiden mutation).
19. Subject has a history of thrombocytopenia, including heparin induced thrombocytopenia.
20. Subject has a known history of hypersensitivity to drugs with a similar chemical structure to enoxaparin sodium (eg, unfractionated heparin, low molecular weight heparin) or to pork products.
21. Subject is a member of the professional or ancillary personnel involved in the study.
22. Subject is deemed not suitable for entry into the study in the opinion of the investigator.
18 Years
45 Years
ALL
Yes
Sponsors
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PRA Health Sciences
INDUSTRY
Rovi Pharmaceuticals Laboratories
INDUSTRY
Responsible Party
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Principal Investigators
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Maria Velinova, MD, PhD
Role: PRINCIPAL_INVESTIGATOR
PRA Health Sciences (PRA) - Early Development Services (EDS)
Other Identifiers
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2015-003489-10
Identifier Type: EUDRACT_NUMBER
Identifier Source: secondary_id
ROV-RO20-2015-01
Identifier Type: -
Identifier Source: org_study_id