Por: RTTNews Health October 14, 2022
Takeda () announced the CHMP of the European Medicines Agency recommended the approval of the company's dengue vaccine candidate, TAK-003, for the prevention of dengue disease caused by any serotype in individuals four years of age and older in Europe and in dengue-endemic countries participating in the parallel EU-M4all procedure. We are one step closer towards the approval of a dengue vaccine that could benefit many of the millions of... + full article
Associated Press USA Health October 15, 2022
LONDON (AP) — The European Medicines Agency on Friday recommended the authorization of a dengue vaccine made by the Japanese pharmaceutical Takeda that could provide a new tool for millions worldwide against the potentially fatal disease.The EU regulator said in a statement... + más
EU regulator recommends clearing Takeda's dengue vaccine | ABC News
EU regulator recommends clearing Takeda's dengue vaccine | WPLG Local 10
ABC News USA Health October 14, 2022
LONDON -- The European Medicines Agency on Friday recommended the authorization of a dengue vaccine made by the Japanese pharmaceutical Takeda that could provide a new tool for millions worldwide against the potentially fatal disease.The EU regulator said in a statement the... + más
EU regulator recommends clearing Takeda's dengue vaccine | Associated Press
WPLG Local 10 USA Health October 14, 2022
LONDON – The European Medicines Agency on Friday recommended the authorization of a dengue vaccine made by the Japanese pharmaceutical Takeda that could provide a new tool for millions worldwide against the potentially fatal disease.The EU regulator said in a statement the... + más
Forbes USA Business October 11, 2022
The Night Eaters by Marjorie Liu and Sana Takeda, published October 11, 2022 by Abrams ComicArtsArt by Sana Takeda Writer Marjorie Liu and artist Sana Takeda are more than tellers of stories: they are makers of worlds. Their New York Times best-selling, multiple award-winning... + más
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RTTNews USA Health September 26, 2022
Biopharmaceutical company Atea Pharmaceuticals, Inc. () announced Monday that the U.S. Food and Drug Administration (FDA) has granted Fast Track Designation to AT-752, a novel, orally administered, direct-acting antiviral for the treatment of dengue virus infection.AT-752, a... + más
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RTTNews USA Health September 24, 2022
Agios Pharmaceuticals, Inc. () announced Friday that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion on September 15, 2022, recommending the granting of a marketing authorization for PYRUKYND (mitapivat)... + más
Gilead Sciences Says CHMP Adopts Positive Opinion To Extend Indication Of Veklury | RTTNews
BridgeBio's NULIBRY Gets Marketing Authorization In The EU For An Ultra-rare Disease | RTTNews
Gilead Sciences, Inc. () announced Friday that the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency (EMA) adopted a positive opinion to extend the indication of Veklury (remdesivir) for the treatment of pediatric patients (weighing at least... + más
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