Pharmacokinetics and clinical outcomes of generic tacrolimus (Hexal) versus branded tacrolimus in de novo kidney transplant patients

• Verfasst von: Arns, Wolfgang [VerfasserIn]
• Verfasst von: Huppertz, Andrea [VerfasserIn]
• Titel: Pharmacokinetics and clinical outcomes of generic tacrolimus (Hexal) versus branded tacrolimus in de novo kidney transplant patients
• Titelzusatz: a multicenter, randomized trial
• Verf.angabe: Wolfgang Arns, Andrea Huppertz, Thomas Rath, Stephan Ziefle, Lars C. Rump, Anita Hansen, Klemens Budde, Lukas J. Lehner, Maria Shipkova, Daniel Baeumer, Irena Kroeger, Christian Sieder, Thomas Klein, and Peter Schenker
• Jahr: 2017
• Umfang: 9 S.
• Fussnoten: Gesehen am 08.08.2018
• Titel Quelle: Enthalten in: Transplantation
• Ort Quelle: Hagerstown, Md. : Lippincott Williams & Wilkins, 1963
• Jahr Quelle: 2017
• Band/Heft Quelle: 101(2017), 11, Seite 2780-2788
• ISSN Quelle: 1534-6080
• DOI: doi:10.1097/TP.0000000000001843
• Datenträger: Online-Ressource
• Sprache: eng
• Sach-SW: Adult
• Sach-SW: Area Under Curve
• Sach-SW: Biopsy
• Sach-SW: Calcineurin Inhibitors
• Sach-SW: Drug Monitoring
• Sach-SW: Drugs, Generic
• Sach-SW: Female
• Sach-SW: Germany
• Sach-SW: Graft Rejection
• Sach-SW: Graft Survival
• Sach-SW: Humans
• Sach-SW: Immunosuppressive Agents
• Sach-SW: Kidney
• Sach-SW: Kidney Transplantation
• Sach-SW: Male
• Sach-SW: Middle Aged
• Sach-SW: Prospective Studies
• Sach-SW: Tacrolimus
• Sach-SW: Therapeutic Equivalency
• Sach-SW: Treatment Outcome
• K10plus-PPN: 1578363195

Abstract

BACKGROUND: Scrupulous comparison of the pharmacokinetic and clinical characteristics of generic tacrolimus formulations versus the reference drug (Prograf) is essential. The pharmacokinetics of the Tacrolimus Hexal (TacHexal) formulation is similar to Prograf in stable renal transplant patients, but data in de novo patients are lacking. METHODS: De novo kidney transplant patients were randomized to generic tacrolimus (TacHexal) or Prograf in a 6-month open-label study. RESULTS: The primary end point, the dose-normalized area under the curve0-12h at month 1 posttransplant, was similar with TacHexal or Prograf; back-transformed geometric means of adjusted log-transformed values (analysis of variance) were 18.99 ng·h·L (TacHexal) and 20.48 ng·h·L (Prograf) (ratio, 1.08; 90% confidence interval, 0.84-1.38; P = 0.605). The dose-normalized peak concentration geometric means at month 1 was also comparable between treatments (ratio, 1.16; 90% confidence interval, 0.88-1.54; P = 0.377). There were no relevant differences in other pharmacokinetic parameters at month 1 or in area under the curve0-4h and trough concentration when measured at months 3 and 6. The adjusted change in mean estimated glomerular filtration rate from baseline to month 6 (Nankivell) was noninferior for TacHexal versus Prograf using observed values (47.7 vs 38.6 mL/min per 1.73 m, P < 0.001) and was superior based on observed values (P = 0.044) but not using last observation-carried forward method. Rates of biopsy-proven acute rejection (5.7% vs 7.9%), adverse events, and serious adverse events were similar with TacHexal or Prograf. CONCLUSION: Tacrolimus pharmacokinetics is similar with TacHexal and Prograf early after kidney transplantation. Efficacy and safety in this limited data set were comparable, with at least equivalent graft function under TacHexal.