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TOGETHER.
LONGER.†

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Vyxeos Liposomal is the first chemotherapy to significantly increase median overall survival (OS)
vs conventional chemotherapy** in patients with high-risk* AML1
(KM-estimated median OS: Vyxeos Liposomal, 9.56 months; conventional chemotherapy, 5.96 months (HR: 0.69, 95% CI: 0.52-0.90, p=0.005 [2-sided])1,2)

Vyxeos Liposomal is indicated for the treatment of adults with newly diagnosed,
therapy-related AML (t-AML) or AML with myelodysplasia-related changes (AML-MRC)2

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Reinforcing Clinical Results
in the Real-World
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Vyxeos Liposomal Data Presentation
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SmPC and Prescribing Information
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What Makes the
Mechanism of Action Different?
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5-Year Follow-Up
Clinical Summary
LAYING THE
foudation
TOWARDS LONG-TERM SURVIVAL
IN HIGH-RISK* AML
This website is intended for European Healthcare Professionals only.
REFERENCES
  • Lancet JE et al. J Clin Oncol 2018;36(26):2684-92.
  • Vyxeos Liposomal. European Summary of Product Characteristics.
  • † Superior overall survival vs conventional chemotherapy** in patients with high-risk * AML 1
  • * High-risk AML is defined as therapy-related acute myeloid leukaemia (t-AML) or AML with myelodysplasia-related changes (AML-MRC)
  • ** Comparator arm conventional chemotherapy is 7+3 in induction, 5+2 in second induction and consolidation where given

ADVERSE EVENTS REPORTING

Adverse events should be reported. Healthcare professionals are asked to report any adverse events via their national reporting system (see Section 4.8 of SmPC). Adverse events should also be reported to Jazz Pharmaceuticals by email to medinfo-int@jazzpharma.com or phone via +353 1 968 1631 (may include an international call charge).

Job code: INT-VYX-2200141
Date of Preparation: September 2022
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