• PG电子黄金城夺宝

    Our Science
    Building a global leading
    synthetic lethality product pipeline
    Our Science
    Approach

    Approach

    The latest data show that cancer has become the second leading cause of death in the world causing 10 million people’s death each year globally. There are huge unmet medical needs for cancer treatment. Since foundation in 2009, IMPACT Therapeutics has been dedicated to the discovery and development of novel anti-cancer therapeutics with global rights, building a global leading synthetic lethality product pipeline to address unmet medical needs and make an impact on cancer treatment.

    Synthetic Lethality

    Genomic instability is one of the hallmarks of cancer cells, and the resultant mutations render cancer cells more dependent on alternative pathways for survival and proliferation, so these cancer cells are more vulnerable to targeted perturbations on those alternative pathways – a phenomenon known as synthetic lethality.

     

    Synthetic lethality is an especially attractive and effective approach to targeting some common oncogenes that have been traditionally considered as undruggable. Synthetic lethality also has the potential to overcome the therapeutic resistance caused by new mutations that often occur with the treatment of conventional targeted therapies. Furthermore, therapies addressing synthetic lethality targets can have anti-tumor effects that are complementary to or synergistic with therapeutics employing other mechanisms. Synthetic lethality can be exploited as a drug development approach to selectively target cancer cells with certain mutations, for example, deficiencies in DNA damage response (DDR), and we see this approach usher in a new paradigm for targeted anti-cancer therapy.

    Pipeline

    Product

    Target

    Pre-clinical

    IND

    Ph I

    Ph II

    Ph III

    Marketed

    Rights

    Collaborations

    IMP4297
    Senaparib
    PARP1/2
    Ovarian Cancer (FLAMES Study, 1L maintenance)
    Ovarian Cancer (SABRINA Study, 3L+,BRCAm)*Pivotal study
    Cell Lung Cancer (combo with Temozolomide)*ODD
    China Commercial
    Partnership with
    Huadong Medicine
    IMP4297
    Senaparib
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    Senaparib, discovered and developed by IMPACT, is a potent and novel PARP1/2 inhibitor. Its distinctive molecular structure ensures exceptional target selectivity and wide therapeutic window.

    The Phase III registrational study (FLAMES) evalsuating Senaparib as a first-line maintenance therapy in advanced ovarian cancer patients (all-comers) has met its primary endpoint, and the the results have been published in the internationally renowned medical journal Nature Medicine.

    Senaparib Capsules (派舒宁® )has received marketing authorization in China from National Medical Products Administration (NMPA) as monotherapy for the maintenance treatment of adult patients with advanced epithelial (FIGO Stages III and IV) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy



    IMP7068
    WEE1
     
    IMP7068
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    IMPACT Therapeutics has identified a novel, potent, and selective WEE1 inhibitor IMP7068. IMP7068 completed phase I clinical study
    IMP9064
    ATR
     
    IMP9064
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    IMP9064, developed by IMPACT, is a potent and highly selective ATR inhibitor. Studies demonstrated that IMP9064 has good oral absorption, and anti-tumor activities in vitro against a broad range of solid tumor cell lines and in vivo against tumor xenograft models. IMP9064 is currently in phase 2 study
    IMP1734
    PARP1-selective
     
    Global Partnership with
    Eikon Therapeutics
    IMP1734
    IMP1707
    PARP1-selective
     
    IMP1707
    IMP13
    USP1
     
    IMP13
    IMP08
    ATM
     
    IMP08
    IMP10
    CHK1/2
     
    IMP10
    IMP5471
    Hedgehog
     
    IMP5471
    中国临床试验
    全球临床试验
    Partnership
    Mutual achievement with professional attitude

    In June 2023, IMPACT entered into a global license and collaboration agreement with Eikon Therapeutics for PARP1 selective inhibitors including IMP1734. Eikon received an exclusive license from IMPACT to co-develop, register, manufacture, and commercialize IMP1734 and other PARP1 selective inhibitors globally, excluding Greater China.

     

    In December 2023, IMPACT entered into commercial partnership with Hangzhou Zhongmei Huadong Pharmaceutical Co., Ltd, a subsidiary of Huadong Medicine Co., Ltd (SZ.000963) for promoting Senaparib. Huadong Medicine received exclusive promotion rights of Senaparib in mainland China.

     

    We intend to continue exploring partnerships through strategic collaborations including licensing arrangements, co-development and co-commercialization arrangements to maximize the clinical and commercial value of our drug candidates.

    Our products
    Lead the new life

    Senaparib, discovered and developed by IMPACT, is a potent and novel PARP1/2 inhibitor. Its distinctive molecular structure ensures exceptional target selectivity and wide therapeutic window.
    The Phase III registrational study (FLAMES) evalsuating Senaparib as a first-line maintenance therapy in advanced ovarian cancer patients (all-comers) has met its primary endpoint, and the the results have been published in the internationally renowned medical journal Nature Medicine.
    Senaparib Capsules (派舒宁® )has received marketing authorization in China from National Medical Products Administration (NMPA) as monotherapy for the maintenance treatment of adult patients with advanced epithelial (FIGO Stages III and IV) high-grade ovarian, fallopian tube or primary peritoneal cancer who are in response (complete or partial) following completion of first-line platinum-based chemotherapy.

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    PG电子黄金城夺宝