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Clinical Trial Summary

This is a Phase 1 dose escalation to assess the safety, tolerability and maximum tolerated dose of subcutaneous administered SDX-7320 in patients with advanced refractory or late-stage solid tumors.


Clinical Trial Description

This is a Phase 1 dose escalation study to assess the safety and tolerability of subcutaneously administered SDX-7320 in patients with advanced refractory or late-stage solid tumors.

Once the MTD has been determined up to 12 patients will be treated at this dose level, to further characterize treatment emergent adverse events (TEAEs). ;


Study Design


Related Conditions & MeSH terms


NCT number NCT02743637
Study type Interventional
Source SynDevRx, Inc.
Contact
Status Completed
Phase Phase 1
Start date February 2016
Completion date December 16, 2019

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