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Last Updated: November 12, 2019

DrugPatentWatch Database Preview

CLINICAL TRIALS PROFILE FOR OPRELVEKIN

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Clinical Trials for Oprelvekin

Trial ID Title Status Sponsor Phase Summary
NCT00493181 Interleukin 11, Thrombocytopenia, Imatinib in Chronic Myelogenous Leukemia (CML) Patients Completed Wyeth is now a wholly owned subsidiary of Pfizer Phase 2 The goal of this clinical research study is to find out if IL-11 (NeumegaTM) may increase the platelet count in patients with Chronic myeloid leukemia (CML) who develop low platelet counts while receiving therapy with imatinib mesylate (Gleevec, STI571), or other tyrosine kinase inhibitors such as AMN107, dasatinib, or SK1606. Primary Objective: 1. To determine efficacy of low-dose interleukin-11, (IL-11, oprelvekin, NeumegaTM) in improving the thrombocytopenia associate with imatinib or other tyrosine kinase inhibitor therapy in patients with CML. Secondary Objective: 1. To determine the safety of low-dose IL-11 in patients with CML and thrombocytopenia associated with imatinib or other tyrosine kinase inhibitors
NCT00493181 Interleukin 11, Thrombocytopenia, Imatinib in Chronic Myelogenous Leukemia (CML) Patients Completed M.D. Anderson Cancer Center Phase 2 The goal of this clinical research study is to find out if IL-11 (NeumegaTM) may increase the platelet count in patients with Chronic myeloid leukemia (CML) who develop low platelet counts while receiving therapy with imatinib mesylate (Gleevec, STI571), or other tyrosine kinase inhibitors such as AMN107, dasatinib, or SK1606. Primary Objective: 1. To determine efficacy of low-dose interleukin-11, (IL-11, oprelvekin, NeumegaTM) in improving the thrombocytopenia associate with imatinib or other tyrosine kinase inhibitor therapy in patients with CML. Secondary Objective: 1. To determine the safety of low-dose IL-11 in patients with CML and thrombocytopenia associated with imatinib or other tyrosine kinase inhibitors
NCT00524225 IL-11 in Adults With Von Willebrand Disease Undergoing Surgery Terminated University of North Carolina Phase 2 The purpose of this study is to determine the efficacy and safety of rhIL-11 when given subcutaneously in adults with type 1 von Willebrand disease undergoing elective surgery or major dental procedure. Efficacy will be measured by estimated blood loss, and frequency and severity of bleeding and transfusion requirement during and after surgery. Safety will be measured by the frequency of adverse events, including fever, headache, fatigue, myalgias, arthralgias, fluid retention, or edema.
NCT00524225 IL-11 in Adults With Von Willebrand Disease Undergoing Surgery Terminated Wyeth is now a wholly owned subsidiary of Pfizer Phase 2 The purpose of this study is to determine the efficacy and safety of rhIL-11 when given subcutaneously in adults with type 1 von Willebrand disease undergoing elective surgery or major dental procedure. Efficacy will be measured by estimated blood loss, and frequency and severity of bleeding and transfusion requirement during and after surgery. Safety will be measured by the frequency of adverse events, including fever, headache, fatigue, myalgias, arthralgias, fluid retention, or edema.
NCT00524225 IL-11 in Adults With Von Willebrand Disease Undergoing Surgery Terminated University of Pittsburgh Phase 2 The purpose of this study is to determine the efficacy and safety of rhIL-11 when given subcutaneously in adults with type 1 von Willebrand disease undergoing elective surgery or major dental procedure. Efficacy will be measured by estimated blood loss, and frequency and severity of bleeding and transfusion requirement during and after surgery. Safety will be measured by the frequency of adverse events, including fever, headache, fatigue, myalgias, arthralgias, fluid retention, or edema.
NCT00524342 IL-11 in Women With Von Willebrand Disease and Refractory Menorrhagia Completed University of North Carolina Phase 2 The purpose of this study is to determine the efficacy and safety of rhIL-11, when given subcutaneously for six consecutive months, in reducing menstrual blood loss in women with type 1 von Willebrand disease and refractory menorrhagia. Efficacy will be measured by subjective bleeding severity scale and pictorial bleeding chart. Safety will be measured by the frequency of adverse events, including fever, headache, fatigue, myalgias, arthralgias, fluid retention, or edema.
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for Oprelvekin

Condition Name

Condition Name for
Intervention Trials
Von Willebrand Disease 2
Severe Thrombocytopenia 1
Leukemia 1
Chronic Myeloid Leukemia 1
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Condition MeSH

Condition MeSH for
Intervention Trials
Von Willebrand Diseases 2
Thrombocytopenia 2
Menorrhagia 1
Leukemia, Myeloid 1
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Clinical Trial Locations for Oprelvekin

Trials by Country

Trials by Country for
Location Trials
United States 8
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Trials by US State

Trials by US State for
Location Trials
Pennsylvania 2
Texas 2
Ohio 1
Kentucky 1
District of Columbia 1
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Clinical Trial Progress for Oprelvekin

Clinical Trial Phase

Clinical Trial Phase for
Clinical Trial Phase Trials
Phase 2 4
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Clinical Trial Status

Clinical Trial Status for
Clinical Trial Phase Trials
Completed 2
Terminated 2
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Clinical Trial Sponsors for Oprelvekin

Sponsor Name

Sponsor Name for
Sponsor Trials
Wyeth is now a wholly owned subsidiary of Pfizer 3
University of Pittsburgh 2
University of North Carolina 2
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Sponsor Type

Sponsor Type for
Sponsor Trials
Other 5
Industry 4
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Serving leading biopharmaceutical companies globally:

Medtronic
Express Scripts
Boehringer Ingelheim
Baxter
Johnson and Johnson
Colorcon

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