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A single-center, open-label, randomized cross-over study to evaluate the pharmacokinetics and bioavailability of once-daily prolonged-release formulations of tacrolimus in de novo liver transplant recipients.

Uta HerdenMartina SterneckBettina M BuchholzEike G AchillesArmin OttLutz Fischer
Published in: Immunity, inflammation and disease (2021)
Despite methodological weaknesses that limit the conclusions, we have found a more consistent drug exposure for LCP-Tac in de novo LT recipients. LCP-Tac demonstrated a greater bioavailability compared to PR-Tac.
Keyphrases
  • open label
  • phase iii
  • phase ii
  • clinical trial
  • double blind
  • phase ii study
  • physical activity
  • emergency department
  • squamous cell carcinoma
  • kidney transplantation
  • adverse drug
  • electronic health record