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Clinical Trial Summary

The purpose of this Phase 1a, first in human, randomized, double-blind, placebo-controlled study is to evaluate the safety, tolerability, PK and PD profile of the orally administered IMR-687 in healthy adult subjects.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT02998450
Study type Interventional
Source Imara, Inc.
Contact
Status Completed
Phase Phase 1
Start date October 18, 2016
Completion date July 8, 2017

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