A Study of Subcutaneous and Intravenous VELCADE in Patients With Previously Treated Multiple Myeloma

PHASE3CompletedINTERVENTIONAL
Enrollment

222

Participants

Timeline

Start Date

July 31, 2008

Primary Completion Date

August 31, 2010

Study Completion Date

September 30, 2010

Conditions
Multiple Myeloma
Interventions
DRUG

VELCADE Administered by subcutaneous injection

Patients will receive a 1.3mg/meters(squared)/dose of VELCADE on Days 1,4,8, and 11 of a 3-week cycle

DRUG

VELCADE Administered by intravenous infusion

Patients will receive a 1.3mg/meters(squared) dose of VELCADE on Days 1,4,8, and 11 of a 3-week cycle.

Trial Locations (3)

1090

UZ Brussel Department Medical Oncology Laarbeeklaan 101, Brussels

44093

Hôtel DIEU, Service D'Hématologie Place Alexis RICORDEAU, Nantes

48129

Universitätsklinikum Münster Onkologische Ambulanz West Albert-Schweitzer-Str. 33, Münster

All Listed Sponsors
collaborator

Johnson & Johnson Pharmaceutical Research & Development, L.L.C.

INDUSTRY

lead

Millennium Pharmaceuticals, Inc.

INDUSTRY