Clinical Trials Directory

Trials / Completed

CompletedNCT03163550

A Study to Assess the Safety, Tolerability, Pharmacokinetics, Food Effect, and Drug-Drug Interaction Potential of ACHN-383 and ACHN-789

A Phase 1 Study to Assess the Safety, Tolerability, Pharmacokinetics, Food Effect, and the Drug-Drug Interaction Potential of Oral ACHN-383 and ACHN-789 in Healthy Subjects

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
40 (actual)
Sponsor
Achaogen, Inc. · Industry
Sex
All
Age
18 Years – 75 Years
Healthy volunteers
Accepted

Summary

This Phase 1 clinical study is a double-blind, randomized, placebo-controlled, parallel group study to assess the safety, tolerability, pharmacokinetics (PK), food effect, and drug interaction potential of ACHN-383 and ACHN-789 co-administered orally as separate capsules in healthy subjects

Conditions

Interventions

TypeNameDescription
DRUGACHN-383Oral dose
DRUGACHN-789Oral dose
DRUGPlaceboOral dose

Timeline

Start date
2017-05-17
Primary completion
2017-10-15
Completion
2017-10-15
First posted
2017-05-23
Last updated
2017-12-02

Locations

1 site across 1 country: Australia

Source: ClinicalTrials.gov record NCT03163550. Inclusion in this directory is not an endorsement.