Page 23 - குழு க்கு மருத்துவ ப்ராடக்ட்ஸ் மனிதன் News Today : Breaking News, Live Updates & Top Stories | Vimarsana

NanoViricides Has Filed Quarterly Report for Period Ending December 31, 2020 - Has Sufficient Cash, Coronavirus Drug Candidate Safe in GLP Safety Toxicology Moving Towards IND

NanoViricides Has Filed Quarterly Report for Period Ending December 31, 2020 - Has Sufficient Cash, Coronavirus Drug Candidate Safe in GLP Safety Toxicology Moving Towards IND
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South africaUnited statesUnited kingdomSouth africanNanoviricides incDrug administrationCompany formExchange commissionCommittee for medicinal products humanTheracour pharma incEuropean medicines agencySecurities exchangeAnil diwanHuman immunodeficiency virusHepatitisb virusHepatitisc virus

Xeris Pharmaceuticals : obtient l approbation de la Commission européenne d Ogluo™ (glucagon) pour injection pour le traitement de l hypoglycémie sévère chez les adultes, les adolescents et les enfants âgés de 2 ans et plus atteints de diabète sucré

Xeris Pharmaceuticals : obtient l approbation de la Commission européenne d Ogluo™ (glucagon) pour injection pour le traitement de l hypoglycémie sévère chez les adultes, les adolescents et les enfants âgés de 2 ans et plus atteints de diabète sucré
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DelveInsight Analysts Expect Beta-Thalassemia Market Size to Expand at a CAGR of 16 3% During the Study Period (2017-2030) in the 6MM

Share this article LAS VEGAS, Feb. 8, 2021 /PRNewswire/ DelveInsight s Beta-Thalassemia Market report offers a holistic picture of the market landscape of the Beta Thalassemia key companies, emerging pipeline therapies, Beta-Thalassemia market share occupied by individual therapies, current and forecasted Beta-thal market share in the 6MM (the US, and EU5 (the UK, Germany, France, Italy, and Spain) for the study period. The report highlights the drivers and constraints shaping the present Beta-Thalassemia Market along with the unmet medical needs that offer opportunities to the key players to explore the underlying potential of the market. Some of the key highlights from the

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Novo Nordisk s Sogroya moves closer towards EU approval

Novo Nordisk’s Sogroya moves closer towards EU approval 2nd February 2021 Novo Nordisk’s Sogroya (somapacitan) has received a positive opinion from the European Medicines Agency’s (EMA) Committee for Medicinal Products for Human Use – moving closer towards approval in the EU. The CHMP has recommended marketing authorisation for Sogroya for the treatment of adults with growth hormone deficiency (AGHD). The recommendation is based on results from the Phase III REAL 1 clinical trial programme, which investigated the efficacy and safety of Sogroya in AGHD. “We are very pleased with the positive opinion for once-weekly Sogroya as we are committed to continuously developing innovative and efficient medicines for people living with growth hormone deficiency,” said Mads Krogsgaard Thomsen, executive vice president and chief scientific officer of Novo Nordisk.

Novo nordisk sogroyaKrogsgaard thomsenCommittee for medicinal products humanEuropean medicines agencyNovo nordiskMedicinal productsHuman useMads krogsgaard thomsenகுழு க்கு மருத்துவ ப்ராடக்ட்ஸ் மனிதன்மருத்துவ ப்ராடக்ட்ஸ்மனிதன் பயன்பாடு

Incyte verkündet CHMP-Empfehlung für Pemigatinib zur Behandlung Erwachsener mit zuvor behandeltem, nicht resezierbarem und lokal fortgeschrittenem oder metastasiertem Cholangiokarzinom

Incyte verkündet CHMP-Empfehlung für Pemigatinib zur Behandlung Erwachsener mit zuvor behandeltem, nicht resezierbarem und lokal fortgeschrittenem oder metastasiertem Cholangiokarzinom
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