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University of Hong Kong develops vaccine against H7N9 avian influenza

 Time of Update: 2020-06-15

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Business Agency, April 2 (Xinhua) -- Chinese mainland and Hong Kong have many people infected with H7N9 avian influenza, the University of Hong Kong research team said, successfully developed a vacci
Weekly Statement: An Analysis of the Protection Boundary of Pharmaceutical Patent Rights and Related Recommendations

 Time of Update: 2020-06-12

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Original title: "Weekly Statement" A brief review of the protection boundary of pharmaceutical patent rights and related proposals to analyze the protection boundary of pharmaceutical patent rights an
FDA has accepted a license for complementary biological products from Mercadon Gardasil 9

 Time of Update: 2020-06-11

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recently, the U.S Pharmaceutical sand announced that the U.S Food and Drug ( FDA ) has accepted a supplementary biologics license (sBLA) for the Gardasil 9 (Plus, 9-price recombinant human papi
New vaccine combined with existing immunotherapy could effectively fight melanoma, study finds

 Time of Update: 2020-06-11

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recently, researchers from the Sprees Institute in San Diego, in collaboration with experts from other institutions, have developed a new vaccine that, in combination with existing immunotherapy tre
FDA accepts new drug application from Roche Hemlibra ® (emicizumab-kxwh)

 Time of Update: 2020-06-11

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recentdays, Roche Pharmaceutical (announced that the U.S FDA (which has accepted the Hemlibra ® (emicizumab-kxwh) for the treatment of adults and children with no type 8 factor inhibitor, hemoph
FDA announces approval of Shionogi's new drug Mulpleta (lusutrombopag) to market

 Time of Update: 2020-06-11

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Today, the U.S FDA announced the approval of Shionogi's new drug to treat specific groups of adult patients with thrombocytopenia These patients also suffer from chronic liver disease and have p
FDA approves first monthly injection of leppenketone long-acting needle to be available for treatment of adult schizophrenia

 Time of Update: 2020-06-11

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recently, the U.S Food and Medicines ( FDA approved the first monthly injection of Perseris, Indivior, for the treatment of adult schizophrenia manufacturers of (it is noted that, by using a
Hao Ding biotech anti-cancer new drug OBI-3424 obtains FDA-issued orphan drug qualification

 Time of Update: 2020-06-11

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HCC is the sixth-largest cancer in the world, but it is rare in the United States, with about 61,483 cases in 2018 HCC is a deadly cancer with a five-year survival rate of 12.2%, the third leading c
Gilead's Ekoun tablets used to treat HIV-1 infection are approved in China

 Time of Update: 2020-06-11

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recently, Gilead Science s (announced that the National Drug (the Supervisory Authority approved the use of Jetcon (Ecoon tablets, or E/C/F/TAF) to treat HIV-1 infection in China, Jetkang is a
EMA grants chikungunya vaccine program priority drug eligibility

 Time of Update: 2020-06-11

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chikungunya fever is an acute infectious disease caused by CHIKV, transmitted by the Aedes aegypti mosquito, characterized by fever, rash and joint pain, with long-term debilitating effects, and the
LYNPARZA for pancreatic cancer treatment obtains FDA-granted orphanage drug designation

 Time of Update: 2020-06-11

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pancreatic cancer is a rare, life-threatening disease that accounts for about 3% of all cancers in the United States Due to the late onset of symptoms, patients are usually diagnosed only after the
FDA accepts biologics license application for PNH in research drug ALXN1210

 Time of Update: 2020-06-11

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recently, Alexion Pharmaceuticals that the FDA , , has accept ed an application for a biological license (BLA) for the of the drug , the Ravulizumab, for a valiant sleeping hemoglobinuria (PNH)
The State Drug Administration has approved Sanofifashuk for uric acid control in children with leukemia and lymphoma

 Time of Update: 2020-06-11

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recently, Sanofi China announced that the National Drug (The Supervisory Authority has recently approved Faschuk (injection with Labrihai) for children with leukemia, lymphoma patients with urinar
Clinical Phase 2 study data for the treatment of child growth hormone deficiency published by Novo nornod

 Time of Update: 2020-06-11

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recently, Novo Nordisk released clinical Phase 2 study data for the treatment of childhood growth hormone deficiency, showing that it has the same effect as the company's ( -day drug (® (®, growt
FDA provisionally approves Bryhali for treatment of plaque-type psoriasis in adult patients

 Time of Update: 2020-06-11

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recently, Bausch Health (and its dermatology company, Ortho Dermatologics) jointly announced that the U.S FDA (provisionally approved Brybetasol propionate, 0.01%) emulsion as a local treatment
The application for the listing of Ravidawe, a hepatitis C innovative drug, was accepted by the State Drug Administration

 Time of Update: 2020-06-11

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recently, the , The of the Limited Company (Co., Inc.), announced that its second new hepatitis C (Ravidasvir, RDV) as the future pan-genotype direct antiviral drug (DAA) was included in the l
FDA has granted GeneTek Xolair ® breakthrough therapy to identify foreheads to prevent food allergies

 Time of Update: 2020-06-11

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recently, Roche's GeneTek announced that the U.S fda (which has granted Xolair ® (omalizumab, Omazumab) breakthrough therapy to prevent accidental exposure to one or more foods can lead to severe
Gene Tektronix's new heavy flu drug Baloxavir marboxil's Phase 3 study CAPSTONE-2 reaches its main destination

 Time of Update: 2020-06-11

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today, Genentech, a member of the Roche Group, announced that the , a new drug to assess the efficacy of a new drug heavy influenza, reached its main destination in the phase 3 study CAPSTONE-2, wh
FDA accepts New Drug Listing Application for Gilteritinib for AML Adult Patient Treatment

 Time of Update: 2020-06-11

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acute myeloid leukemia (AML) is a blood malignant tumor with abnormal proliferation of bone marrow hematopoietic bud cells, and is the most common acute leukemia in adults , Japan's Astellas Pharma
FDA accepts new drug application from Shire's Gattex

 Time of Update: 2020-06-11

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recently, the of the British Pharmaceuticals (The Company) ( the FDA ) has accepted the supplementary new drug (sNDA) for Gattex.com the sNDA application for approval to expand the indication

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Medical Research Articles

University of Hong Kong develops vaccine against H7N9 avian influenza

Weekly Statement: An Analysis of the Protection Boundary of Pharmaceutical Patent Rights and Related Recommendations

FDA has accepted a license for complementary biological products from Mercadon Gardasil 9

New vaccine combined with existing immunotherapy could effectively fight melanoma, study finds

FDA accepts new drug application from Roche Hemlibra ® (emicizumab-kxwh)

FDA announces approval of Shionogi's new drug Mulpleta (lusutrombopag) to market

FDA approves first monthly injection of leppenketone long-acting needle to be available for treatment of adult schizophrenia

Hao Ding biotech anti-cancer new drug OBI-3424 obtains FDA-issued orphan drug qualification

Gilead's Ekoun tablets used to treat HIV-1 infection are approved in China

EMA grants chikungunya vaccine program priority drug eligibility

LYNPARZA for pancreatic cancer treatment obtains FDA-granted orphanage drug designation

FDA accepts biologics license application for PNH in research drug ALXN1210

The State Drug Administration has approved Sanofifashuk for uric acid control in children with leukemia and lymphoma

Clinical Phase 2 study data for the treatment of child growth hormone deficiency published by Novo nornod

FDA provisionally approves Bryhali for treatment of plaque-type psoriasis in adult patients

The application for the listing of Ravidawe, a hepatitis C innovative drug, was accepted by the State Drug Administration

FDA has granted GeneTek Xolair ® breakthrough therapy to identify foreheads to prevent food allergies

Gene Tektronix's new heavy flu drug Baloxavir marboxil's Phase 3 study CAPSTONE-2 reaches its main destination

FDA accepts New Drug Listing Application for Gilteritinib for AML Adult Patient Treatment

FDA accepts new drug application from Shire's Gattex