Overview

Study of Minnelide™ in Patients With Advanced GI Tumors

Status:
Completed
Trial end date:
2016-12-01
Target enrollment:
Participant gender:
Summary
The primary objective of this study is to determine the maximum tolerated dose (MTD) and the dose limiting toxicities (DLT) of Minnelide™ and to establish the dose of Minnelide™ recommended for future phase 2 protocol
Phase:
Phase 1
Details
Lead Sponsor:
Minneamrita Therapeutics LLC
Treatments:
14-O-phosphonooxymethyltriptolide disodium salt