The therapeutic potential of a kallikrein inhibitor for treating hereditary angioedema.

@article{Levy2006TheTP,
  title={The therapeutic potential of a kallikrein inhibitor for treating hereditary angioedema.},
  author={Jerrold H Levy and Penrose S O'Donnell},
  journal={Expert opinion on investigational drugs},
  year={2006},
  volume={15 9},
  pages={1077-90}
}
Hereditary angioedema (HAE) manifests as intermittent, painful attacks of submucosal oedema affecting the larynx, gastrointestinal tract or limbs. Currently, acute treatment is available in Europe but not USA, and requires intravenous administration of a pooled blood product. HAE is most likely caused by dysinhibition of the contact cascade, resulting in overproduction of bradykinin. DX-88 (ecallantide, Dyax Corp.) is a highly specific recombinant plasma kallikrein inhibitor that halts the… CONTINUE READING

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