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PK & Tolerability of CNV1014802 in Young and Elderly Healthy Volunteers

Trigeminal Neuralgia Clinical Trial

Official title:
A Randomized, Double-blind, Placebo Controlled, Two Period Crossover Study to Investigate the Pharmacokinetics, Tolerability and Cognitive Effects of an Oral Dose Regimen of 150mg Tid CNV1014802 in Healthy Young Versus Elderly Male and Female Subjects

Clinical Trial Summary

A randomized, double-blind, placebo controlled, two period crossover study to investigate the pharmacokinetics, tolerability and cognitive effects of 8 days dosing of CNV1014802 in healthy young versus elderly male and female subjects. Treatment periods will be separated by 13 days. The primary outcome measures are pharmacokinetics (PK) and tolerability.

Clinical Trial Description

This study was previously posted by Convergence Pharmaceuticals, Ltd., which has been acquired by Biogen. ;

Study Design

Related Conditions & MeSH terms

Clinical Trial Details
NCT number NCT02359344
Study type Interventional
Source Biogen
Contact
Status Completed
Phase Phase 1
Start date February 3, 2015
Completion date April 20, 2015
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