Trial Search Results

Determination of Safe and Effective Dose of Romiplostim (AMG 531) in Subjects With Myelodysplastic Syndrome (MDS)Receiving Hypomethylating Agents

The purpose of this study is to evaluate the effect of Romiplostim (AMG 531) on the incidence of clinically significant thrombocytopenic events (grade 3 or 4 and/or receipt of platelet transfusions) in subjects with low or intermediate risk Myelodysplastic Syndrome (MDS) receiving hypomethylating agents. It is hypothesized that Romiplostim administration, at the appropriate dose and schedule, will result in reduction in the incidence of clinically significant thrombocytopenic events in low or intermediate risk MDS subjects receiving hypomethylating agents.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:

Amgen

Stanford Investigator(s):

Intervention(s):

  • Drug: Placebo
  • Biological: AMG 531 (Romiplostim)
  • Drug: Azacitidine
  • Drug: Decitabine

Phase:

Phase 2

Eligibility


Inclusion Criteria: - Diagnosis of MDS by bone marrow biopsy based on the World Health
Organization (WHO) classification - Low, Intermediate-1 or Intermediate-2 risk category MDS
using the IPSS (International Prognostic Scoring System) - Planned to receive either
azacytidine 75 mg/m2 by subcutaneous administration each day for 7 days or decitabine 20
mg/m2 by intravenous administration each day for 5 days for at least 4 cycles Exclusion
Criteria:

   - Prior exposure to >3 cycles hypomethylating agents

   - Prior history of leukemia or aplastic anemia

   - Prior history of bone marrow transplantation

   - Prior malignancy (other than in situ cervical cancer or basal cell cancer of the skin)
   unless treated with curative intent and without evidence of disease for ³ 3 years
   before randomization

   - Active or uncontrolled infections

   - Unstable angina, congestive heart failure [NYHA (New York Heart Association) > class
   II], uncontrolled hypertension [diastolic > 100 mmHg], uncontrolled cardiac
   arrhythmia, or recent (within 1 year) myocardial infarction

   - History of arterial thrombosis ( eg, stroke or transient ischemic attack) in the past
   year

   - History of venous thrombosis that currently requires anti-coagulation therapy

   - Received IL-11 within 4 weeks of screening

   - Less than 4 weeks since receipt of any therapeutic drug or device that is not FDA
   approved for any indication

   - Have previously received any other thrombopoietic growth factor

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study

All

Not currently accepting new patients for this trial

Contact Information

Stanford University
School of Medicine
300 Pasteur Drive
Stanford, CA 94305
Mai Tran
6507238594
Not Recruiting