Bioequivalence of generic and branded subcutaneous enoxaparin: a single-dose, randomized-sequence, open-label, two-period crossover study in healthy Chinese male subjects

Clin Ther. 2009 Jul;31(7):1559-67. doi: 10.1016/j.clinthera.2009.07.017.

Abstract

Background: Enoxaparin is a low-molecular-weight heparin (LMWH) indicated for antithrombosis. A branded formulation of subcutaneously administered enoxaparin has been available in China since 2000, and a generic formulation is being developed. In a literature search of the key term enoxaparin (publication years not restricted), no published data were identified regarding the pharmacokinetic profile of generic enoxaparin in Chinese subjects.

Objective: The aim of this study was to determine the bioequivalence of generic (test) and branded (reference) formulations of enoxaparin 60 mg (6000 IU anti-Xa) SC in healthy subjects for the purpose of meeting regulatory requirements for marketing the generic formulation in China.

Methods: Healthy Chinese male volunteers were eligible for this single-dose, randomized-sequence, open-label, 2-period crossover study. Participants were randomly assigned to receive the test and reference formulations of enoxaparin 60 mg SC injection (fasting state) in randomized order, with the 2 study periods separated by a 1-week washout period. For the assessment of anti-Xa and anti-IIa activities (surrogates used to describe the pharmacokinetic properties and bioavailability of LMWH), heparin clotting assay, and activated partial thromboplastin time (aPTT), blood samples were obtained before (hour 0; baseline) and at 0.5, 1, 2, 3, 4, 5, 6, 8, 10, 12, 14, and 24 hours after study drug administration. The 2 formulations were to be considered bioequivalent if the 90% CIs for the logarithm-transformed values of C(max), T(max), AUC(0-t), and AUC(0-infinity) fell within the predetermined range of 80% to 125%. Tolerability was assessed by questioning subjects about symptoms of possible adverse events and using laboratory analysis (hematology, biochemistry, hepatic function tests, and urinalysis).

Results: Twenty-two subjects participated in the study (mean [SD] age, 21.10 [1.02] years [range, 19-23 years]; weight, 64.07 [5.93] kg [range, 54-75 kg]; and height, 173 [5] cm [range, 163-187 cm]). For anti-Xa activity, the 90% CIs of C(max), AUC(0-t), and AUC(0-infinity) were 100.4% to 106.7%, 100.7% to 105.8%, and 100.7% to 106.1%, respectively. Corresponding values for anti-IIa activity were 85.0% to 102.4%, 80.4% to 94.8%, and 80.1% to 96.0%. For the hepa-rin clotting assay, the values were 97.4% to 102.4%, 98.2% to 102.4%, and 96.0% to 102.7%; and for aPTT, values were 98.2% to 104.3%, 97.4% to 101.6%, and 93.4% to 117.4%. No adverse events were reported during the study.

Conclusions: Based on the 90% CIs of anti-Xa and anti-IIa activities, heparin clotting assay results, and aPTT in these healthy Chinese male subjects, the test and reference formulations of enoxaparin 60 mg SC met the regulatory requirements for bio-equivalence. Both formulations were well tolerated.

Publication types

  • Randomized Controlled Trial

MeSH terms

  • Anticoagulants / administration & dosage
  • Anticoagulants / pharmacokinetics*
  • Anticoagulants / pharmacology
  • Area Under Curve
  • Biological Availability
  • Blood Coagulation Tests
  • China
  • Cross-Over Studies
  • Drugs, Generic / administration & dosage
  • Drugs, Generic / pharmacokinetics
  • Drugs, Generic / pharmacology
  • Enoxaparin / administration & dosage
  • Enoxaparin / pharmacokinetics*
  • Enoxaparin / pharmacology
  • Factor Xa Inhibitors
  • Humans
  • Injections, Subcutaneous
  • Male
  • Partial Thromboplastin Time / methods
  • Prothrombin / antagonists & inhibitors
  • Therapeutic Equivalency
  • Young Adult

Substances

  • Anticoagulants
  • Drugs, Generic
  • Enoxaparin
  • Factor Xa Inhibitors
  • Prothrombin
  • Factor IIa