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- W2066232227 endingPage "180" @default.
- W2066232227 startingPage "167" @default.
- W2066232227 abstract "The expanding repertoire of novel, low molecular weight immunosuppressive agents currently undergoing clinical trials in transplant recipients and patients with autoimmune disease offers great promise for the more selective control of the immune response in these populations.' Cyclosporin was the first of these new agents, and was introduced into clinical practice during the early 1980s. In common with cyclosporin, all of the recently developed drugs have been designed to suppress the immune system more specifically than former regimens based on T cell depletion, steroids and azathioprine. However, none is without side-effects, and increasingly large and complex controlled trials are needed to establish the relative clinical merits of these new drugs when compared, or used in combination, with established cyclosporin-based immunosuppression. After extensive multicentre clinical trials in both Europe? and the USA,' the second of these new agents, tacrolimus (FK506), was granted a licence in the UK in June 1994, for use in liver and kidney transplant recipients, for both primary immunosuppression and the treatment of allograft rejection resistant to conventional therapy." @default.
- W2066232227 created "2016-06-24" @default.
- W2066232227 creator A5025128513 @default.
- W2066232227 date "1998-03-01" @default.
- W2066232227 modified "2023-10-18" @default.
- W2066232227 title "Therapeutic Monitoring of Tacrolimus" @default.
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- W2066232227 doi "https://doi.org/10.1177/000456329803500201" @default.
- W2066232227 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/9547889" @default.
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