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Clinical Trial Summary

The purpose of this study is to evaluate the percentage of participants in each sotatercept dose regimen who achieve a hematopoietic response during the treatment period including up to 2 months after the last dose of sotatercept treatment of chemotherapy-induced anemia (CIA) in participants with metastatic breast cancer. Hematopoietic response was defined as an increase in hemoglobin concentration of ≥ 1 g/dL relative to baseline for 28 consecutive days during the treatment period including up to 2 months after the last dose of sotatercept in the absence of red blood cell (RBC) transfusion or treatment with an erythropoiesis-stimulating agent (ESA).


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT00931606
Study type Interventional
Source Merck Sharp & Dohme LLC
Contact
Status Terminated
Phase Phase 2
Start date June 1, 2009
Completion date November 18, 2010

See also
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Completed NCT00144495 - A Study of Recombinant Human Erythropoietin in Anemic Cancer Patients Undergoing Chemotherapy Phase 3
Not yet recruiting NCT06075030 - A Study of AND017 in Cancer Related Anemic Patients Receiving Chemotherapy Phase 2
Completed NCT00144482 - A Study of Recombinant Human Erythropoietin in Anemic Cancer Patients Undergoing Chemotherapy Phase 3
Completed NCT04076943 - Evaluation of Efficacy and Safety of Roxadustat for the Treatment of Chemotherapy Induced Anemia Phase 2