An Efficacy and Safety Study of Decitabine in Participants With Myelodysplastic Syndrome (MDS)

PHASE2CompletedINTERVENTIONAL
Enrollment

37

Participants

Timeline

Start Date

August 31, 2008

Primary Completion Date

September 30, 2010

Study Completion Date

August 31, 2012

Conditions
Myelodysplastic Syndrome
Interventions
DRUG

Decitabine

Decitabine 20 mg per m\^2 will be administered intravenous infusion over 1 hour, once daily for 5 consecutive days of a 28 days cycle up to 8 cycles or continued until disease progression or unacceptable toxicity.

Trial Locations (6)

Unknown

Changhua

Kaohsiung City

Taichung

Tainan City

Taipei

Tau-Yuan County 333

Sponsors
All Listed Sponsors
lead

Johnson & Johnson Taiwan Ltd

INDUSTRY