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  • HP:0012325: Chronic myelomonocytic leukemia
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    HP:0012325: Chronic myelomonocytic leukemia

    Developed by Shray Alag, The Harker School
    Sections: Correlations, Clinical Trials, and HPO

    Correlations computed by analyzing all clinical trials.

    Navigate: Clinical Trials and HPO


    Correlated Drug Terms (2)


    Name (Synonyms) Correlation
    drug2044 IO-202 Dose Escalation Wiki 1.00
    drug2045 IO-202 Dose Expansion Wiki 1.00

    Correlated MeSH Terms (5)


    Name (Synonyms) Correlation
    D015479 Leukemia, Myelomonocytic, Acute NIH 1.00
    D015477 Leukemia, Myelomonocytic, Chronic NIH 1.00
    D007951 Leukemia, Myeloid, NIH 0.71
    Name (Synonyms) Correlation
    D015470 Leukemia, Myeloid, Acute NIH 0.58
    D007938 Leukemia, NIH 0.32

    Correlated HPO Terms (4)


    Name (Synonyms) Correlation
    HP:0004820 Acute myelomonocytic leukemia HPO 1.00
    HP:0012324 Myeloid leukemia HPO 0.71
    HP:0004808 Acute myeloid leukemia HPO 0.58
    Name (Synonyms) Correlation
    HP:0001909 Leukemia HPO 0.24

    Clinical Trials

    Navigate: Correlations   HPO

    There is one clinical trial.


    1 A Phase 1, Multicenter, Open-Label, Dose-Escalation and Expansion Study of Intravenously Administered IO-202 in Patients With Relapsed/Refractory Acute Myeloid Leukemia (AML) and Chronic Myelomonocytic Leukemia (CMML)

    To assess safety and tolerability at increasing dose levels of IO-202 in successive cohorts of participants with relapsed or refractory monocytic AML and CMML in order to estimate the maximum tolerated dose (MTD) or maximum administered dose (MAD) and select the recommended Phase 2 dose (RP2D) and dose schedule as monotherapy.

    NCT04372433
    Conditions
    1. AML M5
    2. AML M4
    3. AML, Nos
    4. Acute Myelogenous Leukemia in Relapse
    5. Myelomonocytic Leukemia, Chronic
    Interventions
    1. Drug: IO-202 Dose Escalation
    2. Drug: IO-202 Dose Expansion
    MeSH:Leukemia Leukemia, Myeloid Leukemia, Myelomonocytic, Acute Leukemia, Myelomonocytic, Chronic Leukemia, Myeloid, Acute
    HPO:Acute megakaryocytic leukemia Acute myeloid leukemia Acute myelomonocytic leukemia Chronic myelomonocytic leukemia Leukemia Myeloid leukemia

    Primary Outcomes

    Description: Incidence of adverse events

    Measure: Safety of IO-202 as measured by incidence of adverse events.

    Time: From first dose of IO-202 to 30 days following last study treatment

    Description: Severity of adverse events

    Measure: Safety of IO-202 as measured by severity of adverse events.

    Time: From first dose of IO-202 to 30 days following last study treatment

    Description: Incidence dose interruptions and dose reductions

    Measure: Tolerability of IO-202 as measured by incidence and duration of dose interruptions and dose reductions of study treatment

    Time: From first dose of IO-202 to 30 days following last study treatment

    Secondary Outcomes

    Description: Maximum concentration (Cmax) of IO-202

    Measure: To characterize the pharmacokinetics (PK) of IO-202 as defined by maximum plasma concentration (Cmax)

    Time: Through study completion, an average of 1 year

    Description: measure area under the curve (AUC) of IO-202

    Measure: To characterize the PK of IO-202 as defined by area under the curve (AUC)

    Time: Through study completion, an average of 1 year

    Description: Measure anti-drug antibodies in plasma.

    Measure: To evaluate the incidence of anti-drug antibodies against IO-202

    Time: Through study completion, an average of 1 year

    Description: Measure response rates in patients with anti-drug antibodies.

    Measure: To measure rates of response to IO-202 in patients with anti-drug antibodies

    Time: Through study completion, an average of 1 year

    Other Outcomes

    Description: Statistical correlation levels of target expression on leukemic blasts with response rate

    Measure: To correlate target expression with response rates

    Time: Through study completion, a average of 1 year

    Description: Statistical correlation of target expression on leukemic blasts with adverse event rates

    Measure: To correlate target expression with rates of adverse events

    Time: Through study completion, a average of 1 year

    Description: Measure immunophenotype of leukemic blasts from bone marrow aspirates after study treatment

    Measure: To evaluate immunophenotype of leukemic blasts after study treatment.

    Time: Through study completion, a average of 1 year

    HPO Nodes


    HPO

    Alphabetical listing of all HPO terms. Navigate: Correlations   Clinical Trials

    Reports

    Data processed on December 13, 2020.

    An HTML report was created for each of the unique drugs, MeSH, and HPO terms associated with COVID-19 clinical trials. Each report contains a list of either the drug, the MeSH terms, or the HPO terms. All of the terms in a category are displayed on the left-hand side of the report to enable easy navigation, and the reports contain a list of correlated drugs, MeSH, and HPO terms. Further, all reports contain the details of the clinical trials in which the term is referenced. Every clinical trial report shows the mapped HPO and MeSH terms, which are also hyperlinked. Related HPO terms, with their associated genes, protein mutations, and SNPs are also referenced in the report.

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