To Examine The Effects Of Lapatinib On Orally And Intravenously Administered Midazolam In Cancer Patients

PHASE1CompletedINTERVENTIONAL
Enrollment

24

Participants

Timeline

Start Date

November 21, 2005

Primary Completion Date

February 8, 2007

Study Completion Date

February 8, 2007

Conditions
Neoplasms, Breast
Interventions
DRUG

Midazolam

Subjects will receive midazolam by oral or IV route on Days 1, 3, 9 and 11. Oral midazolam was supplied as 3 mg tablets; IV midazolam was supplied as 1 milligram per milliliter (mg/L) sterile solution.

DRUG

Lapatinib

Subjects will receive 1500 mg lapatinib by oral route once daily from Day 4.

Trial Locations (2)

27599

GSK Investigational Site, Chapel Hill

03756

GSK Investigational Site, Lebanon

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY