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Clinical Trial Summary

This initial clinical study in the US will be a randomized, double-blind, placebo-controlled, single-dose, dose-escalation, and sequential cohort study to evaluate the safety, tolerability, PK and PD of D-0120-NA in fasting, healthy volunteers (HVs).

In food effect cohort, subjects will each receive 2 doses of D-0120-NA in an open-label manner; once in the fasted state and once in the fed state.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03291782
Study type Interventional
Source InventisBio Inc.
Contact
Status Completed
Phase Phase 1
Start date September 13, 2017
Completion date August 6, 2018

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