Study of Azacitidine to Evaluate Safety and Effectiveness for Chinese Patients With Higher Risk Myelodysplastic Syndrome

PHASE2CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

July 24, 2012

Primary Completion Date

January 29, 2015

Study Completion Date

March 13, 2018

Conditions
Myelodysplastic Syndrome (MDS)
Interventions
DRUG

Azacitidine

Subcutaneous administration of azacitidine 75 mg/m\^2/day for 7 days every 28 days optimally for at least 6 cycles until disease progression, unacceptable toxicity, or treatment discontinuation for any other reason

Trial Locations (11)

100044

Peking University People's Hospital, Beijing

200025

Ruijin Hospital Shanghai Jiaotong University, Shanghai

200233

Shanghai 6th Hospital, Shanghai

215006

The 1st Hospital of Soochow University, Suzhou

300041

Blood Disease Hospital, Chinese Academy of Medical Science and Peking Union Medical College, Tianjin

300200

The 301 Hospital- Chinese PLA General Hospital, Beijing

310003

1st Hospital Zhejiang University (The First Affiliated Hospital of Zhejiang University ), Hangzhou

430000

Wuhan Union Hospital, Wuhan

510080

Guangdong General Hospital, Guangzhou

610041

West China Hospital of Sichuan University, Chengdu

Unknown

The Third Hospital of Peking University, Beijing

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Celgene

INDUSTRY

NCT01599325 - Study of Azacitidine to Evaluate Safety and Effectiveness for Chinese Patients With Higher Risk Myelodysplastic Syndrome | Biotech Hunter | Biotech Hunter