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PI-166 is a small molecule drug initially developed by The University of New South Wales. It is a small organic compound with specific avidity to liver cancer cells and has demonstrated the ability to reduce the growth of rat hepatomas. PI-166 was formulated as a combination of the active compound and a regional delivery vehicle designed to deliver and retain the drug at tumor sites. Its primary therapeutic focus was on neoplasms, particularly liver cancer, but its global highest R&D status is discontinued after reaching Phase 1 clinical trials.
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