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European Commission approves Roche MabThera for treatment of adult patients with moderate to severe normal herpes

 Time of Update: 2020-06-10

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PV is a rare, serious and potentially life-threatening autoimmune disease characterized by progressive pain blistering in the skin and mucous membranes, accounting for about 80% of herpes cases re
Sandex biosimilar Ziextenzo (pegfilgrastim) gets European Commission approval

 Time of Update: 2020-06-10

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recently, Swiss Pharmaceuticals (http:// 's generic unit Sandoz announced that the European Commission (EC) has approved the biosimilar Zixenzo (Pegfilgrastim), for the full adaptation of the alle
New drug Lishimin ® (Lisna peptide injection) New indications have been officially approved by China's State Drug Administration

 Time of Update: 2020-06-10

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Sanofi China has announced that a new drug for the treatment of type 2 diabetes, (http:// the Lissin ® (Lisnapeptide Injection), has been officially approved by China's national drug (http://
European Medicines Agency grants lead drug A4250 for orphan medicine for daredevil atresia

 Time of Update: 2020-06-10

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bile duct atresia is a rare and life-threatening liver disease, and there is no approved treatment drug (http:// recently, the of the http:// the company of Albireo Pharma, announced that the
FDA approves Novartis Egaten for treatment of tablet-sucking disease patients over 6 years of age

 Time of Update: 2020-06-10

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tablet stoma, also known as liver sucking infection, is a neglected tropical disease There are about 2.4 million patients worldwide, and another 180 million people are at risk today, Novartis (ht
Fda grants Therachon company apraglutide treatment for orphan drug for short bowel syndrome

 Time of Update: 2020-06-10

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short bowel syndrome (SBS) is caused by extensive intestinal removal caused by chronic inflammatory bowel disease (IBD), acute events (such as intestinal infarction), or congenital abnormalities re
Puli PharmaceuticalS Injection Volikonazole (200mg) approved by FDA

 Time of Update: 2020-06-10

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recently, Pharmaceutical (http:// announced in a that company (http:// production of the injection vooliconazole (200mg) through the FDA (http:// approval, eligible to sell in the United St
FDA approves Praluent to reduce risk of angina

 Time of Update: 2020-06-10

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recently, Regeneron Pharmaceuticals and Sanofi announced that The FDA (http:// approved a joint development of the praluent to reduce the risk of heart attack, stroke and heart pain in patients w
First three-part tablets approved by Japanese regulators for treatment of hypertension

 Time of Update: 2020-06-10

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recently, Daiichi Sankyo, a Japanese pharmaceutical company, announced that 1.25mg, 2.5mg and 5mg tablets of the esaxerenone had been approved by Japanese regulators to treat high blood pressure Mi
FDA approves listing of interferon gamma (IFN) antibody Gamifant (emapalumab-lzsg)

 Time of Update: 2020-06-10

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today, Sobi and Novimmune SA (http:// jointly announced that the U.S FDA (http:// approved the joint development of the interferon (IFN)antibody Gamifant (emapalumab-lzg) for the treatment of
European Commission approves Mercadon Keytruda for assisted treatment of melanoma and lymph nodes in adult patients

 Time of Update: 2020-06-10

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recently, the cancer immunotherapy giant Merck and Co announced that the European Commission (EC) has approved the PD-1 tumor immunotherapy Keytruda (Chinese commodity name: Creeda, generic name: pe
FDA accelerates approval of Tecentriq joint Abraxane first-line treatment of triple-yin breast cancer

 Time of Update: 2020-06-10

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recently, Genentech announced FDA (http:// accelerated approval of Tecentriq's combination abraxane (albumin yew alcohol) first-line treatment of PD-L1-positive partially rectocted prestage or me
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
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
FDA grants Enzyvant's RVT-801 rare pediatric disease eligibility and fast-track eligibility

 Time of Update: 2020-06-10

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Farber disease is a rare and considered significantly underdiagnosed disease, often misdiagnosed as juvenile isopathic arthritis The disease is caused by mutations in the ASAH1 gene, which cause the
FDA grants AK1/2 inhibitor Olumiant (baricitinib) fast-track eligibility to treat systemic lupus erythematosus

 Time of Update: 2020-06-10

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recently , http:// giant Eli Lilly and partner Incyte http:// announced that the u.S Food and Drug (http:// Administration ( ) of the FDA (http:// had granted JAK1/2 inhibitor, The Baricit
Advances in new research on the bioimmune anti-cancer drug YS-ON-001

 Time of Update: 2020-06-10

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Today, the company, the http:// Pharmaceutical (http:// Limited , announced http:// that the company's immuno-cancer drug (http:// YS-ON-001 has made new research progress, with excellent tum
Baiyang Pharmaceutical metformin new drug Nida in the United States approved by the FDA

 Time of Update: 2020-06-10

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recently, baiyang Pharmaceutical (http:// announced that the company (http:// of high-end generic drugs, the use of osmosis pump-controlled release technology metformin new drug (http:// th
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
Sanofi fexinidazole approved by DRC for treatment of sleeping sickness

 Time of Update: 2020-06-10

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recently, French Pharmaceutical (http:// giant Sanofi announced that fexinidazole has been approved by the Democratic Republic of the Congo (DRC) to treat the tripanos bruceomaiense human African

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Medical Research Articles

European Commission approves Roche MabThera for treatment of adult patients with moderate to severe normal herpes

Sandex biosimilar Ziextenzo (pegfilgrastim) gets European Commission approval

New drug Lishimin ® (Lisna peptide injection) New indications have been officially approved by China's State Drug Administration

European Medicines Agency grants lead drug A4250 for orphan medicine for daredevil atresia

FDA approves Novartis Egaten for treatment of tablet-sucking disease patients over 6 years of age

Fda grants Therachon company apraglutide treatment for orphan drug for short bowel syndrome

Puli PharmaceuticalS Injection Volikonazole (200mg) approved by FDA

FDA approves Praluent to reduce risk of angina

First three-part tablets approved by Japanese regulators for treatment of hypertension

FDA approves listing of interferon gamma (IFN) antibody Gamifant (emapalumab-lzsg)

European Commission approves Mercadon Keytruda for assisted treatment of melanoma and lymph nodes in adult patients

FDA accelerates approval of Tecentriq joint Abraxane first-line treatment of triple-yin breast cancer

ADHD reaches major endpoint in two key Phase 3 clinical trials

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

FDA grants Enzyvant's RVT-801 rare pediatric disease eligibility and fast-track eligibility

FDA grants AK1/2 inhibitor Olumiant (baricitinib) fast-track eligibility to treat systemic lupus erythematosus

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

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

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

Sanofi fexinidazole approved by DRC for treatment of sleeping sickness