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Acute Myeloid Leukemia Clinical
Trials: Targeted Therapies and
Patient Outcomes

What's Inside:

  • Molecular profiling and risk stratification in AML.
  • Endpoints including complete remission and overall survival.
  • Novel agents: FLT3, IDH1/2, and BCL2 inhibitors.
  • Hematologic toxicity monitoring and safety endpoints.
  • Stem cell transplantation and post-remission strategies.
  • Adaptive and basket trial designs for AML subtypes.

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    Acute Myeloid Leukemia

    Acute Myeloid Leukemia (AML) is a life-threatening form of leukemia characterized by the rapid growth of abnormal white blood cells that accumulate in the bone marrow and interfere with the production of normal blood cells.

    The understanding of AML has evolved significantly over the last few decades. Initially, treatments were non-specific and primarily palliative. The introduction of chemotherapy in the mid-20th century marked a significant advancement, although survival rates remained low. The classification of AML into subtypes based on the French-American-British (FAB) system in the 1970s further refined diagnostic and treatment strategies by categorizing the disease based on the morphology and maturity of affected cells. Recent years have seen a shift towards more targeted therapies, driven by deeper molecular and genetic insights.

    iNGENū’s team of researchers and clinicians is dedicated to advancing AML research. Through innovative trial designs and a patient-centered approach, we work to accelerate the development of new treatments that could offer improved options and outcomes for those affected by AML.

    Roughly

    20k

    new cases of AML are diagnosed annually in the United States

    The median age of diagnosis for AML is

    68

    years old

    28%

    The 5-year survival rate for AML is around 28%, varying based on age and other factors

    Our clinical team has over

    120

    years of combined clinical trial experience