Pegorgotein (formerly known as PEG-SOD) was developed by Enzon pharmaceutical as a scavenger of oxygen-derived free radicals. This drug under the trade name DISMUTEC participated in phase III clinical trial in patients with a severe closed head injury. It was found that the drug failed to show a statistically significant difference between the treatment group and the control group. In spite of DISMUTEC exhibited longer circulating half-life and reduced immunogenicity; however, the drug showed insufficient therapeutic effect for this indication. In addition, pegorgotein was studied for patients with reperfusion injury and stroke. However, these studies were also discontinued.
Originator
Approval Year
PubMed
| Title | Date | PubMed |
|---|---|---|
| Arsenic and chromium in drinking water promote tumorigenesis in a mouse colitis-associated colorectal cancer model and the potential mechanism is ROS-mediated Wnt/β-catenin signaling pathway. | 2012-07-01 |
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| Angiotensin II induces oxidative stress in prostate cancer. | 2008-02 |
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| Redox regulation of HIF-1alpha levels and HO-1 expression in renal medullary interstitial cells. | 2003-06 |
Sample Use Guides
In Vivo Use Guide
Sources: https://www.ncbi.nlm.nih.gov/pubmed/10622650
Six to 18 hours before aortic cross-clamping, patients received a single dose of placebo; pegorgotein, 2,000 IU/kg intravenously; or pegorgotein, 5,000 IU/kg intravenously
Route of Administration:
Intravenous
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