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

PHASE1CompletedINTERVENTIONAL
Enrollment

57

Participants

Timeline

Start Date

October 31, 2008

Primary Completion Date

January 31, 2009

Study Completion Date

January 31, 2009

Conditions
Erectile Dysfunction
Interventions
DRUG

moxifloxacin

400mg

DRUG

avanafil

100mg single dose

DRUG

avanafil

800mg single dose

DRUG

sugar pill

single dose

Trial Locations (1)

53704

Covance Phase 1 Clinical Unit, Madison

Sponsors

Collaborators (1)

All Listed Sponsors
collaborator

Covance

INDUSTRY

lead

VIVUS LLC

INDUSTRY

NCT00769041 - A Thorough EKG Safety Study of TA-1790 (Avanafil) | Biotech Hunter | Biotech Hunter