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Uber's anti-epileptic innovative drug Vipit® (Lacacaamine tablets) has been approved by the State Drug Administration

 Time of Update: 2020-06-10

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today, Yousby announced that its anti-epileptic new drug (http:// Vipert ® (Lacacachamine tablets) has been approved by the National Drug (http:// Supervision Authority for adults and adolesce
Zhifei bioenter virus type 71 inactivated vaccine approved by the State Drug Administration for clinical trials

 Time of Update: 2020-06-10

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recently, Zhifei Bio announced that the Company (http:// and its wholly-owned subsidiary Beijing Zhifei Green Bamboo Bio- Pharmaceutical (http:// Co., Ltd developed the "enterovirus type 71 in
FDA approves blockbuster Dupixent extension for treatment of patients aged 12-17 with severe asexual dermatitis

 Time of Update: 2020-06-10

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amyritis, also known as eczema, is a common chronic inflammatory skin disease Its clinical symptoms include dry skin, redness and itching A rash in patients with moderate lytosis may cover most of t
FDA accepts new drug application for Zerbaxa, a Mercado-difada antibiotic

 Time of Update: 2020-06-10

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recently, Pharmaceutical (http:// giant Merck and Co announced that the U.S Food and Drug (http:// Administration of ( FDA (http:// has accepted complementar y of compound antibiotics pr
EMA grants Krystal Biotech Gene Therapy KB103 for treatment of large herpes epidermal softos

 Time of Update: 2020-06-10

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recently, krystal Biotech company (http:// announced that the European Medicines (http:// Authority (EMA) has granted its leading candidate gene therapy KB103 (bercolagene telserpavec) priorit
FDA accelerates approval of Vitrakvi (larotrectinib) for treatment of late-stage or metastatic solid tumors

 Time of Update: 2020-06-10

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protomyglobulin receptor kinase (TRK) fusion tumors, the NTRK gene merges with unrelated genes, leading to the production of mutated TRK proteins today, Loxo Oncology and Bayer (http:// jointly
The State Drug Administration has recently approved the application for registration of the import of the Emmys- and TheU-Z.

 Time of Update: 2020-06-10

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according to the official website of the State Drug Administration, the State Drug (http:// Supervision Authority has recently approved the import registration application for Themesa-Zunad-mono-
European Commission approves head Novartis Luxturna for treatment of hereditary retinal disease

 Time of Update: 2020-06-10

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, Swiss Pharmaceuticals (http:// giant Novartis announced that the European Commission (EC) has approved Luxturna (voretigene neparvoc) to restore and improve vision for children and adults who ha
Horizon Pharma announces end of phase 3 trial of the single-eye anti-eye drug teprotumumab treatment TED

 Time of Update: 2020-06-10

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today, Horizon Pharma announced that it had previously received The FDA's (http:// 's breakthrough therapy determined that orphan drug eligibility and fast-track eligibility in the study of single
CHMP recommends approval of Tecentriq in combination with amatin and chemotherapy for first-line treatment in Patients with NSq NSCLC

 Time of Update: 2020-06-10

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recently, Swiss pharmaceutical (http:// giant Roche announced that the European Medicines (http:// Authority (http:// (http:// Products for human medicine (http:// ) (http:// has issued an
CHMP recommends approval to expand anindications for amp; Aprincyto single-drug treatment

 Time of Update: 2020-06-10

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recently, the European Medicines (http:// Administration (EMA) human Medicines (http:// Product (http:// Committee (CHMP) has issued a positive opinion recommending approval to extend the an
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
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
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
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
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
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
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

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Medical Research Articles

Uber's anti-epileptic innovative drug Vipit® (Lacacaamine tablets) has been approved by the State Drug Administration

Zhifei bioenter virus type 71 inactivated vaccine approved by the State Drug Administration for clinical trials

FDA approves blockbuster Dupixent extension for treatment of patients aged 12-17 with severe asexual dermatitis

FDA accepts new drug application for Zerbaxa, a Mercado-difada antibiotic

EMA grants Krystal Biotech Gene Therapy KB103 for treatment of large herpes epidermal softos

FDA accelerates approval of Vitrakvi (larotrectinib) for treatment of late-stage or metastatic solid tumors

The State Drug Administration has recently approved the application for registration of the import of the Emmys- and TheU-Z.

European Commission approves head Novartis Luxturna for treatment of hereditary retinal disease

Horizon Pharma announces end of phase 3 trial of the single-eye anti-eye drug teprotumumab treatment TED

CHMP recommends approval of Tecentriq in combination with amatin and chemotherapy for first-line treatment in Patients with NSq NSCLC

CHMP recommends approval to expand anindications for amp; Aprincyto single-drug treatment

FDA approves Praluent to reduce risk of angina

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

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

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

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

Puli PharmaceuticalS Injection Volikonazole (200mg) approved by FDA

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