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    Home > Medical News > Medical World News > Under the innovative trend of pharmaceutical companies, local pharmaceutical companies compete for the focus of tumor drug costs

    Under the innovative trend of pharmaceutical companies, local pharmaceutical companies compete for the focus of tumor drug costs

    • Last Update: 2022-05-08
    • Source: Internet
    • Author: User
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    [Pharmaceutical Network Market Analysis] Under the background of the continuous impact of the epidemic, industry changes and intensified competition, the adjustment of the pharmaceutical industry has entered a deep-water period
    .

    At present, in order to avoid the pain of adjustment period and strive for more development opportunities, various pharmaceutical companies are constantly accelerating innovation
    .

    Under the tide of innovation, it is very important to choose a good track.
    On the whole, oncology drugs have become one of the key directions for local pharmaceutical companies to compete
    .

    Statistics show that the number of new drugs approved for marketing in the past five years has reached 15, accounting for more than 60%; biological drugs are concentrated in monoclonal antibodies led by PD-1
    .

    At present, the time has come to 2022.
    According to the author's knowledge, PD-1/PD-L1 products of many companies have been approved for clinical use and marketed
    .

    On April 21, the NMPA website announced that the new anti-tumor drug Procarbazine Hydrochloride Capsules application submitted by Zhaoke Pharmaceutical, a subsidiary of Li's Pharmaceutical Factory, has been approved
    .

    According to an earlier press release issued by Lee's Big Pharma, the indication for this product's approved marketing application is: for the treatment of advanced Hodgkin's lymphoma
    .

       According to public information, procarbazine hydrochloride capsules were originally developed by Roche and have been approved for marketing overseas, and are produced by Leadiant Biosciences (formerly Sigma-Tau)
    .

    A wholly-owned subsidiary of Lee's Pharma signed a distribution agreement with Leadiant in May 2018 to promote the exclusive launch of procarbazine hydrochloride capsules in Greater China
    .

       On April 20, the CDE website announced that a new class 2.
    4 drug named NBTXR3 has obtained an implied license for a clinical trial and is intended to be developed for the treatment of head and neck squamous cell carcinoma
    .

    According to public information, NBTXR3 is a novel radio-enhancer developed by Nanobiotix, which is intended for the treatment of tumors.
    It consists of functionalized hafnium dioxide (HfO2) nanoparticles, which are administered via a one-time intratumoral injection and activated by radiotherapy.

    .

       It is understood that in May 2021, Liantuo announced a partnership with Nanobiotix to obtain the exclusive license to develop and commercialize NBTXR3 in Greater China, South Korea, Singapore and Thailand
    .

    Under the agreement, LianBio will participate in a global Phase 3 head and neck cancer registration study to evaluate the efficacy of NBTXR3 in patients with locally advanced head and neck squamous cell carcinoma (HNSCC)
    .

    Upfront and potential milestone payments for this collaboration are up to $240 million
    .

       Prior to this, Sino Biopharmaceutical also announced that the group's self-developed anti-tumor class I new drug "TQB2930" for injection has been approved by the China National Medical Products Administration to conduct drug clinical trials for the treatment of patients with advanced malignant tumors
    .

    The data show that TQB2930 is a bispecific antibody targeting solid tumor cells, achieving a synergistic effect on the two targets
    .

    It blocks gene signals that drive tumor growth and kills tumor cells through a variety of mechanisms
    .

    Preclinical efficacy trials have shown that the molecule can significantly inhibit tumor growth
    .

       On the whole, under the encouragement of innovative drug policies and centralized procurement policies, the clinical research and development of innovative drugs in China is advancing rapidly
    .

    Among them, the field of anti-tumor drugs, as a hot disease field, is constantly making new progress
    .

    In the context of the acceleration of tumor drug research and development by domestic pharmaceutical companies, Essence Securities estimates that by the end of 2022, a total of 17 PD-1/PD-L1 monoclonal antibodies and 1 PD-1/CTLA-4 double antibody will be listed in China.
    , of which there are 14 domestic PD-1/PD-L1 models (including double antibodies)
    .

       Disclaimer: Under no circumstances does the information or opinions expressed in this article constitute investment advice to anyone
    .

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