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Clinical Trial Summary

This study will evaluate the safety and efficacy of mebendazole (ReposMBZ) in patient with advanced gastrointestinal cancer or cancer of unknown origin. All patients will be given ReposMBZ for 16 weeks continuous treatment, individually dosed based on the serum concentration of mebendazole.


Clinical Trial Description

Mebendazole has been used extensively during long time for local gut helminthic infections at low dose but also at considerably higher doses during months to years against invasive echinococcus infections. Recent research has now clearly indicated that mebendazole has anticancer effect. Given these observations and the experience of excellent tolerance to mebendazole the current clinical trial protocol is based on the repositioning strategy to more extensively investigate whether mebendazole could be developed into a useful anticancer drug. ;


Study Design


Related Conditions & MeSH terms


NCT number NCT03628079
Study type Interventional
Source Repos Pharma
Contact
Status Terminated
Phase Phase 1/Phase 2
Start date May 25, 2018
Completion date January 16, 2019

See also
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