Abstract
Sotrastaurin (AEB-071, NVP-AEB-071) is an orally bioavailable compound that exerts its effects through the selective inhibition of the classic and novel forms of protein kinase C (PKC), thereby inhibiting early T-cell activation and IL-2 production. In preclinical studies, sotrastaurin reduced the rejection of allogeneic solid organ and islet transplants and interacted in a synergistic manner with the immunosuppressive agent ciclosporin. Sotrastaurin is being investigated in a number of clinical trials aimed at exploring its efficacy and safety in T-cell-mediated conditions such as transplant rejection, psoriasis, uveitis and ulcerative colitis. The compound has shown acceptable toxicity profiles in healthy individuals and transplant recipients. Provided sotrastaurin shows continued promise in the ongoing clinical studies, it may be a safe and effective alternative or adjunct to calcineurin inhibitors.
Original language | English (US) |
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Pages (from-to) | 618-623 |
Number of pages | 6 |
Journal | Drugs of the Future |
Volume | 34 |
Issue number | 8 |
DOIs | |
State | Published - Aug 2009 |
Externally published | Yes |
ASJC Scopus subject areas
- Pharmacology
- Pharmacology (medical)