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mardi 12 juin 2018

Akebia Therapeutics Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4) | Business Wire

Akebia Therapeutics Reports Inducement Grants Under NASDAQ Listing Rule 5635(c)(4) | Business Wire: Akebia Therapeutics, Inc. (NASDAQ:AKBA), a biopharmaceutical company focused on delivering innovative therapies to patients with kidney disease throug

FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Previously Treated Patients with Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS Greater Than or Equal to 1) | Business Wire

FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Previously Treated Patients with Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1 (CPS Greater Than or Equal to 1) | Business Wire: FDA Approves Merck’s KEYTRUDA for Previously Treated Patients with Recurrent or Metastatic Cervical Cancer Whose Tumors Express PD-L1

Los resultados del estudio fase III OPTIMISMM presentados en ASCO 2018 mostraron que el triplete PVd mejoraba la SLP en líneas precoces del mieloma múltiple recidivante o refractario | Business Wire

Los resultados del estudio fase III OPTIMISMM presentados en ASCO 2018 mostraron que el triplete PVd mejoraba la SLP en líneas precoces del mieloma múltiple recidivante o refractario | Business Wire: Celgene Corporation (NASDAQ: CELG) anunció hoy los resultados del estudio OPTIMISMM, un ensayo clínico fase III, internacional, aleatorizado, abierto,

ExThera Medical annonce la conclusion de l'essai d'homologation du marquage CE visant à évaluer la sécurité d'emploi du filtre à sang Seraph® 100 | Business Wire

ExThera Medical annonce la conclusion de l'essai d'homologation du marquage CE visant à évaluer la sécurité d'emploi du filtre à sang Seraph® 100 | Business Wire: ExThera Medical Corporation, qui développe des traitements visant à éliminer les bactéries et virus du sang, a annoncé aujourd'hui la conclusion de l'

ContraVir Pharmaceuticals Reminds Investors of Today’s Deadline to be a Shareholder of Record

ContraVir Pharmaceuticals Reminds Investors of Today’s Deadline to be a Shareholder of Record

リヴァノヴァの無縫合大動脈心臓弁パーシバルが日本で承認される | Business Wire

リヴァノヴァの無縫合大動脈心臓弁パーシバルが日本で承認される | Business Wire: 市場をリードする医療技術企業のリヴァノヴァ(NASDAQ:LIVN)(「リヴァノヴァ」または「当社」)は本日、大動脈弁疾患を治療するための当社の無縫合大動脈心臓弁Perceval®(パーシバル)を日本の厚生労働省が承認したと発表しました。 リヴァノヴァ株式会社の川名範明社長は、次のように述べています

Agilent Enables CISH on Dako Omnis | Business Wire

Agilent Enables CISH on Dako Omnis | Business Wire: Agilent Technologies Inc. (NYSE: A) today announced the release of a new accessory kit that enables the company’s Dako Omnis system to analyze tissue