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Merck Mavenclad (Krakowbin tablets) approved by the Swiss Medical Products Authority for the treatment of recurrent remission multiple sclerosis
Time of Update: 2020-06-10
recently, Merck KGaA announced that Mavenclad (cladrine tablets) has been approved by the Swiss Medical (http:// product (http:// Authority for the treatment of highly active recurrent recurren
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European Commission approves Tiwa Ajovy preventive treatment for migraines
Time of Update: 2020-06-10
recently, Israel's Pharmaceutical (http:// giant Teva announced that the European Commission (EC) has approved Ajovy (fremanezumab) 225mg injection pre-charged syringe for adult patients with mig
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Johnson Stelara (ustekinumab) reaches major endpoint in Phase 3 clinical trial for severe ulcerative colitis in treatment
Time of Update: 2020-06-10
today, Janssen, a subsidiary of Johnson and Johnson's company, (http:// , announced that its development of Steeinumab had reached its main end in a phase 3 clinical trial (http:// of severe ul
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FDA approves Xellia Pharmaceuticalready pre-mixed vancomycin injection
Time of Update: 2020-06-10
recently, Xellia Pharmaceutical (http:// company (http:// announced that the U.S Food and Medicines (http:// Administration ( FDA (http:// ) has approved the ready-to-use (RTU) premixed van
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Aishi announced that its original anti-epileptic drug, the anti-epileptic drug Varempanai (Weiketai ®), was accepted for the new drug market in China
Time of Update: 2020-06-10
Recently, , Aishi Announced that its original anti-epileptic drug (http:// (AED) http:// (AED) name: Fycompa ®; Chinese Product Name: ®) in China, New Drug (http:// to be accepted in October
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FDA Grants AstraZeneca MEDI8897 Breakthrough Treatment Designation
Time of Update: 2020-06-10
, pharmaceutical (http:// giant AstraZeneca announced that the u.S Food and Drug (http:// Administration ( FDA (http:// ) has granted MEDI8897 breakthrough treatment designation (BTD) In Marc
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Bollinger Ingeheim's new drug Arti-Cell® Forte to be listed in Europe
Time of Update: 2020-06-10
lameness is a common problem for horses and has an impact on their performance and animal welfare Current treatments cannot address the needs of all cases, and the industry is looking forward to inn
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Arnaud Pharmaceutical Lysooma Virus Product Pelareorep (AN1004) approved by NMPA for clinical trial
Time of Update: 2020-06-10
today, the of the Medicines (http:// announced that its ossotic virus product Pelareorep (AN1004) has been approved by the National Food Medicines (http:// Regulatory Authority (NMPA) clinical
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FDA Grants MB-102 (CD123 CAR-T) Orphan Drug For BPDCN
Time of Update: 2020-06-10
recently, Mustang Bio (http:// announced that the u.S Food and Drug (http:// Administration ( FDA (http:// ) has granted MB-102 (CD123 CAR-T) the status of orphan drug for the treatment of pa
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FDA approves Tosymra for acute treatment for headache attacks in migraine patients
Time of Update: 2020-06-10
recently, Dr Reddy's (http:// and its subsidiary Promius Pharma announced that the U.S FDA (http:// approved the launch of Tosymra as an acute treatment for migraine attacks in migraine patien
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Xi'an Yangsen's Zei yu ® (Acetate Abitron tablets) new indications approved by the State Drug Administration
Time of Update: 2020-06-10
prostate cancer is the most common urogenital cancer in Chinese men, with a national incidence rate of 9.8 per 100,000 people and a high rate of 12.07 percent per year yesterday (December 4), Johns
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Roche submits a license to the FDA to supplement biologics to the anti-cancer drug Kadcyla
Time of Update: 2020-06-10
recently, Roche, the swiss pharmaceutical (http:// giant, announced that it had submitted to the u.S Food and Drug (http:// Administration ( FDA (http:// a supplementary biological product
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A copy of the anti-epileptic drug Fycompa (perampanel, Verlampane) was submitted to THE EMA
Time of Update: 2020-06-10
recently, Eisai, a Japanese drugmaker, announced that it had submitted an application to the European Medicines (http:// Authority (EMA) for the anti-epileptic drug Fycompa (perampana) to approve
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10% of vimpat (lacosamide, lacamide) ® dry syrup is available in Japan
Time of Update: 2020-06-10
recently, Belgium's Pharmaceutical (http:// giant UCB Japan sub- company (http:// UCB Japan Co and First Third Pharmaceuticals announced that 10 percent of the ® dry syrup of The Lacosamide (l
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Xi'an Yangsen-type ® (injection with Invrisi monoantigen) approved by the State Drug Administration
Time of Update: 2020-06-10
Today, Xi'an Yangsen Pharmaceutical (http:// Limited Company (http:// announced that the National Drug (http:// Supervisory Authority has approved the ® (REMICADE®), i.e injected with infri
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Changchun Haiyue Hedara fofi first imitation approved by the State Bureau for listing
Time of Update: 2020-06-10
On February 17, , the State Administration announced the approval of the Drug (http:// , and Changchun Haiyue Tadalajara was approved for the first time Changchun Hyatt Pharmaceuticals declared pro
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Fda approves AYCAZ ® for supplementary listing of cUTI and cIAI for treatment of children over 3 months of time
Time of Update: 2020-06-10
recently, Allergan (http:// announced that the U.S FDA http:// has approved its drug (http:// AVYCAZ ® (ceftazidime-cephalosporine and avibactam) for complex intra-abdominal infections (cUT
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FDA approves Precigen's PRGN-3006 Research New Drug (IND) Application
Time of Update: 2020-06-10
Precigen, a of intrexon's wholly owned company, (http:// signed a new licensing agreement with Ziopharm in October , however, Precigen announced that FDA (http:// has approved its prGN-3006 re
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Intercept reaches major end in phase 3 trial of new drug Ocacic acid (OCA)
Time of Update: 2020-06-10
NASH is a progressive liver disease caused by excessive accumulation of fat in the liver, which can lead to chronic inflammation of the liver, trigger progressive liver fibrosis, cirrhosis, and ultim
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CHMP expresses support for bluebird bio's application for listing of Genenology Zynteglo
Time of Update: 2020-06-10
recently, bluebird bio announced that the European Medicines (http:// Authority (EMA) has expressed its support for its application for approval (MAA) for gene therapy Zynteglo (formerly Known le