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Clinical Trial Summary

This is a Phase 2, open-label, 2-part, multicenter study in subjects with MSS relapsed/refractory colorectal cancer. The primary objective of Part 1 is to evaluate the safety and tolerability of escalating doses of eFT508 in combination with a fixed dose of avelumab to determine the maximum tolerated dose (MTD) of eFT508 and to select a recommended dose for Part 2. The primary objective of Part 2 is to evaluate antitumor activity of eFT508 at the recommended dose in combination with avelumab or eFT508 monotherapy. Parts 1 and 2 will also evaluate pharmacokinetics (PK) and pharmacodynamics.


Clinical Trial Description

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Study Design


Related Conditions & MeSH terms


NCT number NCT03258398
Study type Interventional
Source Effector Therapeutics
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Status Completed
Phase Phase 2
Start date September 18, 2017
Completion date May 13, 2019