Modeling and simulation to support dose selection and clinical development of SC-75416, a selective COX-2 inhibitor for the treatment of acute and chronic pain

Clin Pharmacol Ther. 2008 Jun;83(6):857-66. doi: 10.1038/sj.clpt.6100374. Epub 2007 Sep 19.

Abstract

Pharmacokinetic/pharmacodynamic (PK/PD) models were developed and clinical trial simulations were conducted to recommend a study design to test the hypothesis that a dose of SC-75416, a selective cyclooxygenase-2 inhibitor, can be identified that achieves superior pain relief (PR) compared to 400 mg ibuprofen in a post-oral surgery pain model. PK/PD models were developed for SC-75416, rofecoxib, valdecoxib, and ibuprofen relating plasma concentrations to PR scores using a nonlinear logistic-normal model. Clinical trial simulations conducted using these models suggested that 360 mg SC-75416 could achieve superior PR compared to 400 mg ibuprofen. A placebo- and positive-controlled parallel-group post-oral surgery pain study was conducted evaluating placebo, 60, 180, and 360 mg SC-75416 oral solution, and 400 mg ibuprofen. The study results confirmed the hypothesis that 360 mg SC-75416 achieved superior PR relative to 400 mg ibuprofen (DeltaTOTPAR6=3.3, P<0.05) and demonstrated the predictive performance of the PK/PD models.

Publication types

  • Comparative Study

MeSH terms

  • Acute Disease
  • Benzopyrans / administration & dosage*
  • Chronic Disease
  • Computer Simulation* / trends
  • Controlled Clinical Trials as Topic / methods*
  • Controlled Clinical Trials as Topic / trends
  • Cyclooxygenase 2 / blood
  • Cyclooxygenase 2 Inhibitors / administration & dosage*
  • Dose-Response Relationship, Drug
  • Humans
  • Models, Biological*
  • Pain / blood
  • Pain / drug therapy*
  • Pain / enzymology

Substances

  • Benzopyrans
  • Cyclooxygenase 2 Inhibitors
  • SC-75416
  • Cyclooxygenase 2