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Generated: December 18, 2018

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CLINICAL TRIALS PROFILE FOR VYXEOS

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Clinical Trials for Vyxeos

Trial ID Title Status Sponsor Phase Summary
NCT02533115 EAP of CPX-351 (VYXEOS) for Patients 60-75 Years of Age With Secondary AML Available Celator Pharmaceuticals N/A This study is a Phase IV Expanded Access Protocol (EAP) of CPX-351 in patients with secondary acute myeloid leukemia who are suitable for treatment with intensive chemotherapy.
NCT03555955 A Trial to Evaluate the Potential Impact of Renal Impairment on the Pharmacokinetics and Safety of CPX-351 Not yet recruiting Jazz Pharmaceuticals Phase 1 This study evaluates the pharmacokinetics and safety of CPX-351 in patients with moderate or severe renal impairment.
NCT03572764 CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome Not yet recruiting Jazz Pharmaceuticals Phase 1 This is a pilot and feasibility study of transplant eligible, higher risk myelodysplastic syndrome (MDS) patients to determine the safety and tolerability of a lower -dose and higher-dose CPX-351 regimen, with secondary objectives including complete remission (CR) rates and proportion of patients proceeding to transplant.
NCT03572764 CPX-351 (Vyxeos™) for Transplant Eligible, Higher Risk Patients With Myelodysplastic Syndrome Not yet recruiting Washington University School of Medicine Phase 1 This is a pilot and feasibility study of transplant eligible, higher risk myelodysplastic syndrome (MDS) patients to determine the safety and tolerability of a lower -dose and higher-dose CPX-351 regimen, with secondary objectives including complete remission (CR) rates and proportion of patients proceeding to transplant.
NCT03575325 Vyxeos(CPX-351) in Adults w R/R Acute Lymphoblastic Leukemia Recruiting Jazz Pharmaceuticals Phase 2 This study involves Vyxeos (CPX-351), a formulation of a fixed combination of the two anti-tumor drugs, cytarabine and daunorubicin that will be given as an infusion over 90 minutes. This study will use what is called a "liposome" injection. This is a special fat capsule (called a liposome) that surrounds the cytarabine and daunorubicin and protects the drugs from being eliminated/destroyed by the body.
NCT03575325 Vyxeos(CPX-351) in Adults w R/R Acute Lymphoblastic Leukemia Recruiting H. Lee Moffitt Cancer Center and Research Institute Phase 2 This study involves Vyxeos (CPX-351), a formulation of a fixed combination of the two anti-tumor drugs, cytarabine and daunorubicin that will be given as an infusion over 90 minutes. This study will use what is called a "liposome" injection. This is a special fat capsule (called a liposome) that surrounds the cytarabine and daunorubicin and protects the drugs from being eliminated/destroyed by the body.
Trial ID Title Status Sponsor Phase Summary

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Clinical Trial Conditions for Vyxeos

Condition Name

Condition Name for Vyxeos
Intervention Trials
Refractory Acute Myeloid Leukemia 2
Recurrent Acute Myeloid Leukemia 2
Myelodysplastic Syndromes 2
Acute Lymphoblastic Leukemia 2
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Condition MeSH

Condition MeSH for Vyxeos
Intervention Trials
Leukemia 4
Preleukemia 3
Myelodysplastic Syndromes 3
Leukemia, Myeloid, Acute 3
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Clinical Trial Locations for Vyxeos

Trials by Country

Trials by Country for Vyxeos
Location Trials
United States 12
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Trials by US State

Trials by US State for Vyxeos
Location Trials
Texas 2
Florida 2
Washington 1
Missouri 1
New York 1
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Clinical Trial Progress for Vyxeos

Clinical Trial Phase

Clinical Trial Phase for Vyxeos
Clinical Trial Phase Trials
Phase 2 2
Phase 1 2
N/A 1
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Clinical Trial Status

Clinical Trial Status for Vyxeos
Clinical Trial Phase Trials
Not yet recruiting 3
Recruiting 2
Available 1
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Clinical Trial Sponsors for Vyxeos

Sponsor Name

Sponsor Name for Vyxeos
Sponsor Trials
Jazz Pharmaceuticals 3
M.D. Anderson Cancer Center 2
National Cancer Institute (NCI) 2
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Sponsor Type

Sponsor Type for Vyxeos
Sponsor Trials
Other 4
Industry 4
NIH 2
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