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    Home > Medical News > Latest Medical News > Carrick first in class oral CDK7 inhibitor phase IIa clinical results are positive

    Carrick first in class oral CDK7 inhibitor phase IIa clinical results are positive

    • Last Update: 2021-11-05
    • Source: Internet
    • Author: User
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    The article comes: Medical Rubik's Cube Info

    Author: Shi Bei

    On September 16, Carrick Therapeutics announced the preliminary clinical data of the first in class oral CDK7 inhibitor samuraciclib (CT-7001) at the ESMO 2021 conference
    .

    CDK7 regulates the transcription of oncogenes, promotes uncontrolled cell cycle progression and resistance to antihormonal therapy
    .
    Samuraciclib is a first in class oral CDK7 inhibitor under development


    .


    This phase IIa study aims to evaluate the clinical efficacy and tolerability of samuraciclib combined with fulvestrant in the treatment of hormone receptor positive (HR+), HER2-advanced breast cancer (BC) patients
    .
    A total of 31 refractory patients were enrolled in the study


    .


    Of the 24 patients with evaluable efficacy, 17 patients (71%) had tumor shrinkage
    .
    2 cases (8%) achieved partial remission (PR), and 13 cases (54%) had stable disease (SD)


    .


    The median progression-free survival (mPFS) of the intention-to-treat group (ITT) was 16.
    1 weeks (n=31)
    .
    It is worth noting that the mPFS of patients without mutations in the TP53 gene was 32.


    0 weeks (n=18)


    At baseline, patients without liver metastases (n=17) experienced significant prolonged disease control and had not yet reached mPFS
    .
    At the end of this data, mPFS will be at least 28 weeks


    .


    The main adverse events were low-grade, reversible and controllable gastrointestinal (GI) events through standard preventive treatment.
    No significant neutropenia or bone marrow suppression related to other CDK inhibitors was observed
    .

    In addition to the above research, Carrick is exploring the therapeutic potential of samuraciclib in triple-negative breast cancer (TNBC), prostate cancer, pancreatic cancer, ovarian cancer and colorectal cancer
    .
    Samuraciclib has obtained Fast Track designation from the US Food and Drug Administration (FDA) and is used in combination with Fulvestrant to treat CDK4/6 resistant HR+ and HER2-advanced breast cancer, as well as combined chemotherapy to treat locally advanced or metastatic TNBC


    .


    Note: The original text has been deleted

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