Study of Sotatercept for the Treatment of Anemia in low-or Intermediate-1 Risk Myelodysplastic Syndromes (MDS) or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)
Status: | Completed |
---|---|
Conditions: | Blood Cancer, Anemia |
Therapuetic Areas: | Hematology, Oncology |
Healthy: | No |
Age Range: | 18 - Any |
Updated: | 6/16/2018 |
Start Date: | November 28, 2012 |
End Date: | April 30, 2018 |
An Open-label, Randomized, Phase 2, Parallel, Dose-Ranging, Multicenter Study of Sotatercept for the Treatment of Patients With Anemia and Low or Intermediate-1 Risk Myelodysplastic Syndromes or Non-proliferative Chronic Myelomonocytic Leukemia (CMML)
The primary objective of this study is to determine a safe, tolerable and effective dose of
sotatercept that results in the greatest frequency of improvement of anemia in patients
diagnosed with low- or intermediate-1 risk MDS or non-proliferative chronic myelomonocytic
leukemia (CMML).
sotatercept that results in the greatest frequency of improvement of anemia in patients
diagnosed with low- or intermediate-1 risk MDS or non-proliferative chronic myelomonocytic
leukemia (CMML).
Inclusion Criteria:
- Men and women ≥ 18 years of age
- Documented diagnosis of myelodysplastic syndromes (MDS) or non-proliferative chronic
myelomonocytic leukemia (CMML), White blood cells (WBC) ≤ 13,000 /mm3, World Health
Organization (WHO)) that meets International Prognostic Scoring System (IPSS) criteria
for low or intermediate-1 risk disease
- Anemia, Hemoglobin (Hgb) ≤ 9.0 g/dL or ≥ 2 units of Red Blood Cells (RBCs) within 84
days
- No response or loss of response to Erythropoiesis-Stimulating Agents (ESAs) or
erythropoetin (EPO) > 500 mU/ml
- Eastern Cooperative Group (ECOG) score ≤2.
- Creatinine < 1.5 X Upper Limit of the Normal (ULN)
- Total bilirubin ≤3.0 mg/dL
- Aspartate aminotransferase (AST)/Serum glutamic oxaloacetic transaminase (SGOT) &
Alanine Aminotransferase (ALT)/Serum Glutamic Pyruvic (SGPT) ≤3.0 x Upper Limit of
Norma (ULN)
- Free of metastatic malignancy (other than MDS) for ≥2 years
- Highly effective methods of birth control for females & males
Exclusion Criteria:
- Chromosome 5q deletion
- Pregnant or breast feeding women and males who do not agree to use condom during the
sexual contact with females of childbearing potential.
- Major surgery within 30 days
- Incomplete recovery or incomplete healing of wounds from previous surgery
- Heart failure ≥3 (New York Heart Association(NYHA))
- Thromboembolic or myocardial infarction event within 6 months
- Concurrent anti-cancer cytotoxic chemotherapy
- History of severe allergic or anaphylactic reaction or hypersensitivity to recombinant
protein
- Known positive for Human Immunovirus (HIV) or infectious Hepatitis type C or active
infectious Hepatitis type B.
- Clinically significant anemia unrelated to MDS
- Thrombocytopenia (<30,000/uL)
- Uncontrolled hypertension
- Treatment with another investigational drug or device within 28 days prior to Day 1
- Prior Exposure to Sotatercept (ACE-011)
- Any serious medical condition, lab abnormality or psychiatric illness
We found this trial at
14
sites
Virginia Oncology Associates Virginia Oncology Associates is an oncology and hematology practice of physicians, specializing...
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4502 Medical Drive
San Antonio, Texas 78284
San Antonio, Texas 78284
(210) 567-7000
University of Texas Health Science Center at San Antonio The University of Texas Health Science...
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12902 USF Magnolia Dr
Tampa, Florida 33612
Tampa, Florida 33612
(888) 663-3488
H. Lee Moffitt Cancer Center & Research Institute Moffitt Cancer Center in Tampa, Florida, has...
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Johns Hopkins The Johns Hopkins University opened in 1876, with the inauguration of its first...
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