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NCT Number: NCT00472290

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.

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Key information

Conditions

Hematology Blood Platelet Disorders Bone Marrow Diseases Cytopenia Hematologic Diseases Hemic and Lymphatic Diseases MDS Myelodysplastic Syndromes Thrombocytopenia

Age range

18 year and older

Sex eligibility

All sexes

Study type

Interventional

Phase

Not applicable

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

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 therapy
  • 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 agent(s)/device(s)
  • 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

Treatment and study plan

Romiplostim (formerly AMG 531)

Drug

Subjects will begin the study at an initial dose of 750 µg.

Except for:

  • Subject whose doses were escalated to doses higher than 750 µg AMG 531 weekly, and maintained a response per IWG guidelines for platelet response.
  • Subjects who were stable at a lower dose of AMG 531 on the previous study. Doses will be adjusted throughout the study based on individual subject's platelet count.

Primary outcomes

  1. Overall Summary of Adverse Events

    Time frame: During treatment period from first dose of IP to End of Study visit, on Average 56 Weeks .

  2. Incidence of Antibody (AB) Formation

    Time frame: During treatment period from first dose of IP to End of Study visit, on Average 56 Weeks.

Secondary outcomes

  1. Weekly Bleeding Events Per 100 Subject Years

    Time frame: During the treatment period. The average duration of romiplostim exposure is 56 weeks.

    During the time since the first dose of IP to the end of the treatment period. A single bleeding event was defined as each individual bleeding episode that originated from a specific organ system (eg, gastrointestinal system or central nervous system). A bleeding event that continued for more than 7 days was counted as separate events every eighth day.

  2. Platelet Transfusion Events Per 100 Subject Years

    Time frame: During the treatment period. The average duration of romiplostim exposure is 56 weeks.

    During the time since the first dose of IP to the end of the treatment period. A discrete platelet transfusion event was defined as any number of platelet transfusions administered within a 3-day period. Platelet transfusions administered more than 3 days apart were counted as separate platelet transfusion events.

  3. Weeks With Platelet Response Per Year

    Time frame: During the treatment period. The average duration of romiplostim exposure is 56 weeks.

    During the time since the first dose of IP to the end of the treatment period. Platelet response was based on the modified IWG 2006 criteria (Cheson et al, 2006) and was defined as, in the absence of platelet transfusion: an absolute increase in platelet count of ≥ 30 x 10^9/L for a subject starting with a platelet count of ≥ 20 x 10^9/L; or an increase in platelet count from < 20 x 10^9/L to ≥ 20 x 10^9/L and by at least 100% in a subject that started with a platelet count < 20 x 10^9/L.

  4. Time to First Platelet Response

    Time frame: During treatment period. The average duration of romiplostim exposure is 56 weeks.

    Time since first dose of IP to the first platelet response. Platelet response was based on the modified IWG 2006 criteria (Cheson et al, 2006) and was defined as, in the absence of platelet transfusion: an absolute increase in platelet count of ≥ 30 x 10^9/L for a subject starting with a platelet count of ≥ 20 x 10^9/L; or an increase in platelet count from < 20 x 10^9/L to ≥ 20 x 10^9/L and by at least 100% in a subject that started with a platelet count < 20 x 10^9/L.

  5. Duration of Platelet Response

    Time frame: During treatment period. The average duration of romiplostim exposure is 56 weeks.

    Platelet response was based on the modified IWG 2006 criteria (Cheson et al, 2006) and was defined as, in the absence of platelet transfusion: an absolute increase in platelet count of ≥ 30 x 10^9/L for a subject starting with a platelet count of ≥ 20 x 10^9/L; or an increase in platelet count from < 20 x 10^9/L to ≥ 20 x 10^9/L and by at least 100% in a subject that started with a platelet count < 20 x 10^9/L.

Sponsors and collaborators

Lead sponsor

Amgen

Industry

Registry information

Official study title

An Open Label Extension Study Evaluating the Safety of Long Term Dosing of Romiplostim in Thrombocytopenic Subjects With Myelodysplastic Syndromes (MDS)

Important dates

Study start
2007
Primary completion
2011
Study completion
2011
First posted
May 11, 2007
Registry last updated
Dec 29, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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