Study to Assess the Pharmacokinetics and Pharmacodynamics of GSK461364 in Subjects With Non-Hodgkins Lymphoma

PHASE1CompletedINTERVENTIONAL
Enrollment

41

Participants

Timeline

Start Date

August 16, 2007

Primary Completion Date

September 29, 2009

Study Completion Date

September 29, 2009

Conditions
Lymphoma, Non-Hodgkin
Interventions
DRUG

GSK461364

GSK461364 will be given intravenously as a 4 hour infusion in either a final volume of 500 or 1000 mLs. The starting dose for Stage A - Schedule 1 was 50 mg and doses were to be escalated as described in protocol until maximum tolerated dose established.

Trial Locations (3)

SM2 5PT

GSK Investigational Site, Sutton

BT9 7AB

GSK Investigational Site, Belfast, Northern Ireland

W12 0NN

GSK Investigational Site, London

Sponsors

Lead Sponsor

All Listed Sponsors
lead

GlaxoSmithKline

INDUSTRY