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Methafluoluothantinib listing application approved for treatment of chronic adult patients with chronic myeloid leukemia
Time of Update: 2020-06-07
recently, it was reported that the listing application for methionate flumartinibinib (product name: Haussen-Fu) was approved for the treatment of chronic myeloid leukemia (Ph-CML) chronic adult pat
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Gilead announces new clinical research data on hepatitis B functional cure new drug GS-9688
Time of Update: 2020-06-07
recently, Gilead, the giant of pharmaceutical (http:// released new clinical research data on the functional cure the new drug (http:// Gs-9688( selgantolimod) About GS-9688 GS-9688 is an or
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Key Phase 2 trial of DS-8201, co-developed by AstraZeneca and Phase III, reaches the main research end
Time of Update: 2020-06-07
today, AstraZeneca and Daiichi Sankyo company (http:// announced that the joint development of antibody conjugate drug (http:// (aDC) (fam-8201), in the treatment of HER2-positive metastatic b
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Novo Nordisk Valley Gate Winter Double Insulin Injection (Novo and Jia ®) officially launched in China
Time of Update: 2020-06-07
recently, Novo Nordisk announced that the world's first soluble double insulin degudurd double insulin injection (Novo and Jia ®) has been officially launched in China to treat type 2 diabetes in ad
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Scientists develop a new drug candidate for breast cancer
Time of Update: 2020-06-07
recently, scientists have discovered a new drug (http:// that could starve or suffocate cancer stem cells, paving the way for new treatments for breast cancer patients The study at the Universi
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The phase 3 trial of Takeda protease inhibitor Ninlaro (ixazomib) reaches the main end of the trial
Time of Update: 2020-06-07
today, Takeda (http:// announced that its protease inhibitor Ninlaro (ixazomib) as a first-line maintenance therapy, in the treatment of adult patients with multiple myeloma (MM) without stem cel
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NMPA approves Theiboantium drug Fycompa for treatment of seizures at age 12 and over
Time of Update: 2020-06-07
Recently, Eisai, a Japanese pharmaceutical company, announced that China's National Drug (http:// Regulatory Authority (NMPA) has approved a new generation of anti-epileptic drug Fycompa (perampa
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Three companies jointly conduct clinical trials of antibody-linked drug enfortumab vedotin and Keytruda to treat urinary skin cancer
Time of Update: 2020-06-07
Recently, Seattle Genetics and Astellas announced a partnership agreement with Mercadon to jointly conduct a clinical trial (http:// for the treatment of pre-local advanced or metastatic urinary
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Weishi's new drug, ® (FYCOMPA®), has been approved by China's State Drug Administration
Time of Update: 2020-06-07
recently, the State Medicines (http:// Administration of China has approved the use of the Weishi New Drug (http:// The ® (FYCOMPA®) for the use of adults and children 12 years and older with
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And platinum medicine next-generation all-human anti-CTLA-4 antibody HBM4003 first patient has been successfully enrolled in the group medication
Time of Update: 2020-06-07
recently, and platinum Medicine sin pharmaceutical (http:// announced that its new generation of all-human anti-CTLA-4 antibody HBM4003 has launched the first global clinical trial (http:// fo
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Noten Jianhua BTK inhibitor Obitini ICP-022 new drug listing application accepted
Time of Update: 2020-06-07
recently, it has been reported that the http:// high-selective and irreversible small molecule Bruton tyrosine kinase (BTK) inhibitor Obitini ICP-022 developed by Innocare has been accepted for the
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FDA supports new treatment for Amarin's Vascepa capsule
Time of Update: 2020-06-07
, Amarin (http:// announced that the U.S FDA (http:// endocrine metabolism drug (http:// Advisory (http:// Committee (EMDAC) supports the company's development of Vascepa capsules as a new
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U.S. FDA grants Kiniksa's rilonacept breakthrough therapy
Time of Update: 2020-06-07
today, Kiniksa Pharmaceuticals (http:// announced that the U.S FDA (http:// granted its determination to treat recurrent enticatis (RP) in the il-1 signaling pathway inhibitor rilonacept Abou
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FDA grants Brynering Ingeheim's breakthrough drug
Time of Update: 2020-06-07
The u.S food and drug (http:// Administration ( FDA (http:// has granted its oral small molecule tyrosine kinase inhibitor, Oftedanib, Nidanibu, a breakthrough drug qualification (BTD), the ge
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FDA approves AstraZeneca BTK inhibitor Calquence (acalabrutinib) for treatment of CLL or SLL
Time of Update: 2020-06-07
today, the u.S FDA (http:// announced approval of AstraZeneca (http:// of the BTK inhibitor Calquence (calabrutinib) as an initial or follow-up therapy for the treatment of chronic lymphatic l
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FDA approves lenVIMA and KEYTRUDA for treatment of patients with advanced endometrial cancer
Time of Update: 2020-06-07
today, Atva and Mershadon announced that the U.S Food and Drug (http:// Administration ( FDA (http:// ) has approved a combination of LENVIMA (Chinese) and KEYTRUDA (Chinese) for the treatment
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NMPA accepts application sufaninib for new drug from Huang Chinese pharmaceutical company Surufatinib
Time of Update: 2020-06-07
The National medicines (http:// Regulatory Authority (NMPA ) has accepted the application for listing of the new drug (http:// for the treatment of advanced non-pancreatic neuroendocrine tumor
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Skyfall And MorphoSys Announces CD38 Antibody (TJ202/MOR202) licensed by China's State Drug Administration clinical trial
Time of Update: 2020-06-07
recently, Tianyuan Biotech (Shanghai) Limited Company (http:// ("Tianyuan Bio") and Germany's MorphoSys Corporation announced that human source monoclonal CD38 antibody (TJ202/MOR202) was approve
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Seattle's small molecule tyrosine kinase inhibitor tucatinib key phase 3 trial reaches primary and secondary endpoints
Time of Update: 2020-06-07
today, Seattle Genetics (http:// announced that its HER-specific oral small molecule tyrosine kinase inhibitor tucatinib, in the treatment of pre-local advanced or metastatic HER2-positive breast
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FDA approves GlaxoSmithKline niraparib for treatment of terminal ovarian cancer
Time of Update: 2020-06-07
Today, the U.S FDA (http:// announced that it has approved GlaxoSmithKline (GSK) company (http:// niraparib(name Zejula) extended indications for the treatment of patients with advanced ovaria