Your browser doesn't support javascript. This means that the content or functionality of our website will be limited or unavailable. If you need more information about Vinnova, please contact us.

Development of small molecular immunomodulating anticancer drugs using mebendazol as template

Reference number
Coordinator Uppsala universitet - Institutionen för immunologi, genetik och patologi
Funding from Vinnova SEK 1 000 000
Project duration June 2016 - June 2017
Status Completed

Purpose and goal

The project goal is to develop a new type of immune activating cancer drug, to be be formulated for oral administration. We observed that mebendazole, now in use for parasitic infections, is cytotoxic to cancer cells but also activates macrophages to become anti-tumoral. Anti-cancer activity has been verified in a few pilot patients. We now plan for a clinical trial with a new formulation of mebendazole. In parallel we have synthesized mebendazol analogoues, tested them in our laboratory models and identified a few with properties as good as or better than those of mebendazole.

Expected results and effects

A new formulation or mebendazole to be used in the clinical trial is now under production. The study protocol is finalized an includes sampling for the identification of biomarkers for mebendazole activity. A number of mebendazole analogues have been synthesized and a few identified suitable for CD selection for further development. However, more analogues are to be synthesized prior to CD selection.

Planned approach and implementation

The clinical trial will include up to 50 patients with advanced cancer of gastrointestinal origin. Mebendazole analogues will be designed and synthesized in collaboration with a medicinal chemist, followed by testing in our in vitro models that allow us to identify molecules with properties making them suitable for CD selection and drug development.

The project description has been provided by the project members themselves and the text has not been looked at by our editors.

Last updated 25 November 2019

Reference number 2016-00762

Page statistics