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Evaluate Safety and Pharmacokinetics of Minocin (Minocycline) for Injection in Subjects With Renal Insufficiency

Healthy Subjects Clinical Trial

Official title:
A Phase I, Open-Label, Single-Dose Trial To Determine The Safety And Pharmacokinetics Of Minocin (Minocycline) For Injection In Subjects With Renal Insufficiency

Clinical Trial Summary

This is a Phase 1, open-label, single-dose study of the safety, tolerability, and pharmacokinetics of Minocin® (minocycline) for injection in subjects with renal insufficiency.

Clinical Trial Description

The purpose of this study is to collect safety, tolerability, and pharmacokinetics (PK) data on a single dose of Minocin® (minocycline) for Injection in subjects with renal insufficiency and in subjects receiving hemodialysis therapy. The safety, tolerability, and PK data will support the compound as a potential clinical candidate in Europe and will inform the development of future Phase 2/3 studies. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02808052
Study type Interventional
Source Melinta Therapeutics, Inc.
Contact
Status Terminated
Phase Phase 1
Start date May 29, 2017
Completion date June 4, 2018
View Details
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