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Aishi Corporation announces China's listing of tyrosine kinase inhibitor LeWeima ®

 Time of Update: 2020-06-10

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CHMP recommends approval of Lynparza as a single-drug therapy for adult patients with breast cancer

 Time of Update: 2020-06-10

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, the giant a pharmaceutical (http:// and partner Merck and Co announced in that the European (http:// Authority products for human medicine (http:// http:// Committee (CHMP) has issued a p
European Commission approves split dose scheme for Johnson and Johnson Darzalex

 Time of Update: 2020-06-10

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, the European Commission (EC) has approved Darzalex's split dose plan, the , a http:// company owned by the u.S pharmaceutical (http:// http:// ) giant, , announced the program will provide
Bayer's new gynaecological drug, Visanne, has been approved by Chinese regulators to treat endometriosis

 Time of Update: 2020-06-10

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, Germany's pharmaceutical (http:// giant Bayer announced that , the http:// new drug in the of gynaecology, , was approved by Chinese regulators for the treatment of endometriosis (EMs) Visanne
CHMP recommends neo-base Revlimid's triple therapy for the treatment of patients with multiple myeloma

 Time of Update: 2020-06-10

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recently, Celgene company (http:// announced that the European EMA human medicine (http:// product (http:// Committee (CHMP) recommended that the company's triple therapy based on Revlimid (
FDA grants CymaBay Therapeutics Clinical Phase 3 In Research Drug Seladelpar Breakthrough Therapy Determination

 Time of Update: 2020-06-10

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primary bile bile ductitis is a potentially life-threatening liver autoimmune disease As the immune system continues to attack bile ducts, bile flow is blocked and silted, toxic bile acid remains in
Lizhu Medicine "recombination of whole human source anti-OX40 monoclonal antibody injection" clinical trial application accepted by the State Drug Administration

 Time of Update: 2020-06-10

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recently, the Pharmaceutical (http:// announced that its holding affiliated company (http:// Zhuhai Lizhu single anti-biotechnology Co., Ltd declared "recombination of all-human source anti-OX
FDA approves Sanofi sugar-lowering drug Soliqua ® 100/33 expansion

 Time of Update: 2020-06-10

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recently, the U.S Food and Drug (http:// Administration ( FDA (http:// ) approved the expanded use of Sanofi's sugar-lowering drug Soliqua ® 100/33 (insulin glargine and lisine peptide injectio
Knopp Biosciences announces oral candidate drug dexpramipexole for FDA orphan drug designation

 Time of Update: 2020-06-10

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high eosinophil syndrome (HES) mainly refers to the patient's blood the number of eosinophils continued to increase (the absolute number of eosinophils is greater than 0.5 x 109/L), clinical manifes
FDA approves Janssen Pharmaceuticals Tremfya ® One Pres for treatment in adult patients with moderate to severe plaque psoriasis

 Time of Update: 2020-06-10

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recently, the U.S Pharmaceutical (http:// http:// giant , , janssen Pharmaceutical (http:// announced that the U.S FDA http:// has approved Tremfya ® One Press, a single-dose, patient-co
Diabetes innovative oral therapy imeglimin successfully in a Phase 3 clinical trial

 Time of Update: 2020-06-10

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recently, Poxel Bio Medicines (http:// http:// and partner Sumitomo Dayou Pharmaceutical son (http:// announced the success of its innovative diabetes innovation oral therapy, imeglimin, in
FDA approves shire's treatment of chronic isophation of Motegroity

 Time of Update: 2020-06-10

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FDA approves Pfizer Ibrance joint drug to treat male breast cancer patients

 Time of Update: 2020-06-10

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recently, Pfizer (http:// announced that the U.S FDA (http:// approved the company's heavy-weight breast cancer treatment Ibrcicsito in conjunction with aromatase inhibitors or fuforvestts to
Baiyang Pharmaceutical metformin new drug Nida in the United States approved by the FDA

 Time of Update: 2020-06-10

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Sanofi dengue vaccine Dengvaxia has been approved by the European Commission

 Time of Update: 2020-06-10

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A new drug application from FDA's new base, Lenalidomide, to naldomide

 Time of Update: 2020-06-10

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recently, bio pharmaceutical (http:// giant, Http:// announced that the u.S Food and Drug (http:// Administration ( FDA ( http:// had accepted and granted priority review to a application
ADHD reaches major endpoint in two key Phase 3 clinical trials

 Time of Update: 2020-06-10

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ADHD, commonly known as ADHD, is a chronic brain disease that manifests itself as unable to concentrate, hyperactivity and impulsiveness today, Supernus Pharmaceuticals (http:// announced that i
Advances in new research on the bioimmune anti-cancer drug YS-ON-001

 Time of Update: 2020-06-10

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Fda has janson TREMFYA ® One-Press for treatment of moderate to severe plaque psoriasis

 Time of Update: 2020-06-10

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recently http:// , the U.S FDA (http:// has approved the company's TREMFYA ® One-Press, a one-time, single-dose patient self-controlled syringe for the treatment of moderate to severe plaque psor
Xi'an Yangsen Yiyi (Ibtini capsule) New indications approved by the State Drug Administration

 Time of Update: 2020-06-10

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Medical Research Articles

Aishi Corporation announces China's listing of tyrosine kinase inhibitor LeWeima ®

CHMP recommends approval of Lynparza as a single-drug therapy for adult patients with breast cancer

European Commission approves split dose scheme for Johnson and Johnson Darzalex

Bayer's new gynaecological drug, Visanne, has been approved by Chinese regulators to treat endometriosis

CHMP recommends neo-base Revlimid's triple therapy for the treatment of patients with multiple myeloma

FDA grants CymaBay Therapeutics Clinical Phase 3 In Research Drug Seladelpar Breakthrough Therapy Determination

Lizhu Medicine "recombination of whole human source anti-OX40 monoclonal antibody injection" clinical trial application accepted by the State Drug Administration

FDA approves Sanofi sugar-lowering drug Soliqua ® 100/33 expansion

Knopp Biosciences announces oral candidate drug dexpramipexole for FDA orphan drug designation

FDA approves Janssen Pharmaceuticals Tremfya ® One Pres for treatment in adult patients with moderate to severe plaque psoriasis

Diabetes innovative oral therapy imeglimin successfully in a Phase 3 clinical trial

FDA approves shire's treatment of chronic isophation of Motegroity

FDA approves Pfizer Ibrance joint drug to treat male breast cancer patients

Baiyang Pharmaceutical metformin new drug Nida in the United States approved by the FDA

Sanofi dengue vaccine Dengvaxia has been approved by the European Commission

A new drug application from FDA's new base, Lenalidomide, to naldomide

ADHD reaches major endpoint in two key Phase 3 clinical trials

Advances in new research on the bioimmune anti-cancer drug YS-ON-001

Fda has janson TREMFYA ® One-Press for treatment of moderate to severe plaque psoriasis

Xi'an Yangsen Yiyi (Ibtini capsule) New indications approved by the State Drug Administration