A Phase 2 Study of Lenalidomide to Evaluate the Efficacy in Japanese Patients With Newly Diagnosed Multiple Myeloma

PHASE2CompletedINTERVENTIONAL
Enrollment

26

Participants

Timeline

Start Date

October 1, 2012

Primary Completion Date

November 26, 2013

Study Completion Date

June 26, 2018

Conditions
Multiple Myeloma
Interventions
DRUG

Lenalidomide

25 mg oral lenalidomide once daily on Days 1-21 of each 28-day cycle

DRUG

dexamethasone

40 mg oral dexamethasone once daily on Days 1, 8, 15 and 22 of each 28-day cycle

Trial Locations (24)

466-8650

Nagoya Daini Red Cross Hospital, Nagoya

467-8602

Nagoya City University Hospital, Nagoya

296-8602

Kameda Medical Center, Kamogawa

286-8523

Japanese Red Cross Narita Hospital, Narita

791-0295

Ehime University Hospital, Touon

377-8511

Nishigunma National Hospital, Shibukawa

650-0047

Kobe City Medical Center General Hospital, Kobe

317-0077

Hitachi General Hospital, Hitachi

020-8505

Iwate Medical University, Morioka

259-1193

Tokai University Hospital, Isehara

980-8574

Tohoku University Hospital, Sendai

710-8602

Kurashiki Central Hospital, Kurashiki

589-8511

Kinki University Hospital, Faculty of Medicine, Sayama

411-8777

Shizuoka Cancer Center, Sunto

190-0014

National Disaster Medical Center, Tachikawa

892-0853

Kagoshima Medical Center, Kagoshima

602-8566

University Hospital, Kyoto Prefectural University of Medicine, Kyoto

951-8566

Niigata Cancer Center Hospital, Niigata

701-1192

Okayama Medical Center, Okayama

543-8555

Osaka Red Cross Hospital, Osaka

104-0045

National Cancer Center Hospital, Tokyo

135-8550

The Cancer Institute Hospital of Japanese Foundation for Cancer Research, Tokyo

150-8935

Japanese Red Cross Medical Center, Tokyo

160-8582

Keio University Hospital, Tokyo

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY