Sotrastaurin and Tacrolimus Coadministration: Effects on Pharmacokinetics and Biomarker Responses

• Published in: Journal of clinical pharmacology 2010-11, Vol.50 (11), p.1260-1266
• Main Authors: Kovarik, John M., Stitah, Sylvie, Slade, Alan, Vitaliti, Alessandra, Straube, Frank, Grenet, Olivier, Winter, Serge, Sfikas, Nikolaos, Seiberling, Michael
• Format: Article
• Language: English
• Subjects: Adult; Area Under Curve; Biomarkers - metabolism; Calcium - metabolism; Cell Proliferation - drug effects; Cross-Over Studies; Drug Interactions; Humans; Immunomodulators; Immunosuppressive Agents - pharmacokinetics; Immunosuppressive Agents - pharmacology; Interleukin-2 - metabolism; Lymphocyte Activation - drug effects; Lymphocytes - drug effects; Lymphocytes - metabolism; Male; protein kinase C; Protein Kinase C - antagonists & inhibitors; Pyrroles - pharmacokinetics; Pyrroles - pharmacology; Quinazolines - pharmacokinetics; Quinazolines - pharmacology; RNA, Messenger - drug effects; RNA, Messenger - metabolism; sotrastaurin; T-Lymphocytes - metabolism; tacrolimus; Tacrolimus - pharmacokinetics; Tacrolimus - pharmacology; Tumor Necrosis Factor-alpha - drug effects; Tumor Necrosis Factor-alpha - metabolism; Young Adult
• ISSN: 0091-2700; 1552-4604
• DOI: 10.1177/0091270009360534

Sotrastaurin is an immunosuppressant that inhibits protein kinase C. In the prevention of acute rejection in organ transplantation, sotrastaurin might be combined with tacrolimus. A drug interaction study was performed in 18 healthy subjects who received single oral doses of sotrastaurin 400 mg, tacrolimus 7 mg, and the drug combination. Drug blood levels and lymphocyte activation and proliferation were measured. Tacrolimus did not alter the pharmacokinetics of sotrastaurin; however, sotrastaurin increased tacrolimus area under the concentration‐time curve by 2.0‐fold (90% confidence interval, 1.8–2.1). Production of interleukin‐2 and tumor necrosis factor by T cells activated via calcium‐independent pathways was inhibited by 75% ± 22% from baseline by sotrastaurin. Interleukin‐2 messenger RNA levels were decreased by 90% ± 9% from baseline by sotrastaurin. Addition of tacrolimus to sotrastaurin had minimal or no effect on these biomarkers, consistent with tacrolimus' mechanism of action. Lymphocyte proliferation induced via calcium‐dependent pathways was decreased from baseline by 82% ± 9% by sotrastaurin, 76% ± 11% by tacrolimus, and 96% ± 2% for the drug combination. How sotrastaurin and tacrolimus could be partnered in an immunosuppressive regimen will need to be established in the context of controlled clinical trials in organ transplant patients, taking into account the pharmacokinetic interaction on tacrolimus and the potentially enhanced immunosuppressive activity of this drug combination.