Trial Search Results

Evaluating the Safety of Long Term Dosing of Romiplostim (Formerly AMG 531) in Thrombocytopenic Subjects With Myelodysplastic Syndromes (MDS)

This is an open label extension study of romiplostim for treatment of thrombocytopenia (platelet count ≤ 50 x 10^9/L) in MDS subjects. The study is designed to assess the long-term safety of treatment with romiplostim, as measured by incidence of overall adverse events, the incidence of bleeding events, the utilization of platelet transfusions, and the duration of platelet response. The study will further describe the time to disease progression to acute myeloid leukemia (AML) and survival.

Stanford is currently not accepting patients for this trial.

Lead Sponsor:


Stanford Investigator(s):


  • Drug: Romiplostim (formerly AMG 531)




Inclusion Criteria

   - Subject completed a romiplostim study for the treatment of thrombocytopenia in
   subjects with MDS

   - Subject has an Eastern Cooperative Oncology (ECOG) performance status of 0 to 2

   - Subject had a platelet count ≤ 50 x 10^9/L since the final dose of investigational
   product in the parent study

   - Subject or his/her legally acceptable representative provided written informed consent
   before any study-specific procedures were initiated

Exclusion Criteria

   - Subject has been diagnosed with AML or has a blast count ≥ 10% by peripheral blood or
   bone marrow biopsy

   - Subject has a prior history of leukemia

   - Subject has a prior history of bone marrow or stem cell transplantation

   - Subject has a prior malignancy (other than in situ cervical cancer, controlled
   prostate cancer, or basal cell cancer of the skin) unless treated with curative intent
   and without evidence of disease for ≥ 3 years before randomization

   - Subject has active or uncontrolled infections

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

   - Subject has a history of arterial thrombosis (eg, stroke or transient ischemic attack)
   in the past year

   - Subject has a history of venous thrombosis that currently requires anti-coagulation

   - Subject received interleukin (IL)-11 within 4 weeks of screening

   - Subject previously received a thrombopoietic growth factor (other than romiplostim)

   - Subject has a known hypersensitivity to any recombinant E coli-derived product (eg,
   Infergen®, Neupogen®, Somatropin, Actimmune)

   - Subject is currently enrolled in investigational device or drug study(ies), has not
   yet completed at least 4 weeks since ending investigational device or drug study(ies)
   (other than parent romiplostim study), or subject is receiving other investigational

   - Subject is of child-bearing potential and is evidently pregnant (eg, positive human
   chorionic gonadotropin [HCG] test) or is breast feeding

   - Subject is not using adequate contraceptive precautions

   - Subject has any kind of disorder that compromises his/her ability to give written
   informed consent (and does not have a legally acceptable representative) or is unable
   to comply with study procedures

Ages Eligible for Study

18 Years - N/A

Genders Eligible for Study


Not currently accepting new patients for this trial

Contact Information

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