Overview

A Thorough EKG Safety Study of TA-1790 (Avanafil)

Status:
Completed
Trial end date:
2009-01-01
Target enrollment:
Participant gender:
Summary
This study is to assess whether treatment with a therapeutic (100 mg) or supratherapeutic (800 mg) dose of avanafil has the potential to cause QT/QTc prolongation in healthy volunteers.
Phase:
Phase 1
Details
Lead Sponsor:
VIVUS, Inc.
Collaborator:
Covance
Treatments:
Fluoroquinolones
Moxifloxacin
Norgestimate, ethinyl estradiol drug combination