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Hengrui PharmaceuticalS SHR6390 approved clinical lying for the treatment of recurrent or metastatic breast cancer
Time of Update: 2020-06-07
yesterday, it was revealed that Hengrui Medicine (http:// SHR6390 tablets approved for clinical use in the combination of fluorovis group treatment HR-positive, HER2-negative after endocrine thera
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European Commission approves two options for treating HNSCC patients in Mercadon Keytruda
Time of Update: 2020-06-07
recently, Mersadon announced that the European Commission (EC) has approved two options for Keytruda (Corida, generic name: pembrolizumab, Pablozumab), a first-line treatment of patients with metast
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Takeda releases latest data on phase 3 clinical trials of the quadnage dengue vaccine TAK-003
Time of Update: 2020-06-07
recently, Takeda company (http:// released the latest data from its quadrat dengue vaccine, TAK-003, in the key phase 3 clinical trial (http:// TIDES THE OVERALL VACCINE EFFICACY (VE) OF TAK-
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Xcovery's ALK inhibitor ensartinib (X-396) Phase 2 clinical trial yields positive results
Time of Update: 2020-06-07
recently, Xcovery (http:// announced that its ALK inhibitor ensartinib (X-396) had positive results in the treatment of alK-positive non-small cell lung cancer (NSCLC) patients in the phase 2 cli
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Kadmon's key trial of oral selective ROCK2 inhibitor KD025 reached the main endpoint
Time of Update: 2020-06-07
today, Kadmon announced that its use in the treatment of chronic transplant anti-host disease (cGVHD) in the study of oral selective ROCK2 inhibitor KD025, in the critical test (http:// ROCKstar
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Uber reaches primary and secondary endpoints in the study of IL-17A/F single anti-drug bimekizuma in key Phase 3 trials
Time of Update: 2020-06-07
recently, UCB announced that bimekizumab, the (http:// of the substance IL-17A/F mono-anti- drug for the treatment of chronic moderate to severe plaqueps (plaquepsis), had reached two common prim
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Lilly IL-17 inhibitor Taltz (ixekizumab) two clinical trials reach primary and secondary endpoint
Time of Update: 2020-06-07
today, Eli Lilly (http:// announced that its IL-17 inhibitor Taltz (ixekizumab) has reached its primary and all critical secondary in two clinical trials (http:// treating patients with active
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FDA U.S. Approves APR APR-TD011 Research Drug for Large Herpes Epidermis to Be Certified as Orphan Drug
Time of Update: 2020-06-07
Recently, the (http:// of the Research of the Pharmaceutical (http:// of the Swiss APR Applied Pharmaceutical s (http:// announced that the U.S Food and Medicines (http:// Administration (
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Voclosporin with mycophenolic acid and low-dose steroids in combination with the treatment of lupus nephritis key 3-phase bed trial struck positive results
Time of Update: 2020-06-07
recently, Aurinia Pharmaceuticals (http:// announced that the company's development of voclosporin, in combination with mycophenolic acid (MM) and low-dose steroids, reached all major and critica
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Yan Jian and Alkermes jointly developed Vumerity (diroximel fumarate) with provisional FDA approval
Time of Update: 2020-06-07
recently, Biogen and Alkermes company (http:// to develop a new recurrent type of multiple sclerosis (MS) new treatment, Vumerity (diroximel fumarate), received provisional approval for the FDA
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China's State Drug Administration approves application for new drug ® by Astellas Acostin
Time of Update: 2020-06-07
Today, the http:// Group of the Pharmaceuticals (http:// announced that china's national Drug (http:// Supervisory Authority on November 18 approved the listing of the (http:// ) of the of
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Trovagene PLK1 inhibitor onvansertib (PCM-075) obtains positive early trial data
Time of Update: 2020-06-07
today, Trovagene (http:// announced that it had obtained positive experimental early data in the treatment of 1b/2 clinical trial strial sin (http:// ) in patients with metastatic colorectal ca
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Seattle's oral small molecule tyrosine kinase inhibitor tucatinib 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 HER2-positive metastatic breast cancer patients in th
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GSK developed the triavement of chronic obstructive pulmonary disease Trelegy Ellipta approved by the National Drug Administration for listing
Time of Update: 2020-06-07
Recently, GSK developed the chronic obstructive pulmonary disease (COPD) tri-therapy fluorobutikason ume bromoquine Verantro inhalation powder mist agent (Trelegy Ellipta) approved by the State Drug
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FDA approves Novartis Adakveo (crizanlizumab, also known as SEG101) for listing
Time of Update: 2020-06-07
recently, Novartis (http:// announced that the U.S FDA (http:// approved the launch of its potential heavy-duty therapy, Adaklizumab, also known as SEG101, to reduce the frequency of vascular
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Baxter Squibb CC-486 Maintenance Therapy Treats AML Patients In Phase 3 Key Trials Get Positive Results
Time of Update: 2020-06-07
today, The (http:// of Baxter's Squibb Company announced that its CC-486, as a maintenance therapy, achieved a statistically significant improvement in total survival (OS) and non-recurrent survi
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MHLW approves Alexion's Soliris (eculizumab) for a new indication
Time of Update: 2020-06-07
Recently, Alexion company (http:// announced that the Ministry of Health, Labour and Welfare (MHLW) has approved a new indication of Soliris (eculizumab) for the treatment of anti-water channel p
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Zhengda Tianqing anti-tumor drug injection with hydrochloric acid benzostin has been issued by the State Drug Administration drug registration approval
Time of Update: 2020-06-07
recently, China Bio Pharmaceutical (http:// issued a notice that affiliated company (http:// Zhengda Tianqing Pharmaceutical Group, the anti-tumor drug injection with hydrochloric acid benzodi
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Phase Libtayo clinical trials developed by Regenerative Element and Sanofi show good results
Time of Update: 2020-06-07
Regeneron company (http:// recently announced that its PD-1 inhibitor Libalo,developed with Sanofi, as a single-drug therapy, has shown significantly better results in the first-stage treatment o
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Inovio announces that its INO-5401 combination therapy extends progression-free survival in Phase 1/2 clinical trials treating GBM
Time of Update: 2020-06-07
Today, Inovio Pharmaceuticals (http:// announced that it is working on T-cell activation immunotherapy INO-5401, which is composed of immunoactive agent INO-9012, Libtayo (cemiplimab) Combined th