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The Pharma Letter
6 小时
Ipsen’s Iqirvo approved in Europe
The European Commission has conditionally approved the marketing application submitted by Ipsen for Iqirvo (elafibranor) 80mg ...
The Pharma Letter
7 小时
FluMist approved for self-administration in the USA
On Friday, the US Food and Drug Administration approved UK pharma major AstraZeneca’s (LSE: AZN) FluMist for self- or ...
The Pharma Letter
1 天
Trump vs Harris—who's on Big Pharma's side?
US presidential election, health policy will remain a key issue for pharma. Both Donald Trump and Kamala Harris have ...
The Pharma Letter
1 天
Achilles Thera shifts focus to new cancer treatment avenues
Achilles Therapeutics has announced it will discontinue its tumor-infiltrating lymphocyte (TIL)-based clonal neoantigen T ...
The Pharma Letter
1 天
FDA approves first Niemann-Pick disease, type C treatment
Today, the US Food and Drug Administration approved Miplyffa (arimoclomol), an oral medication for the treatment of ...
The Pharma Letter
1 天
Wegovy label should be extended, CHMP recommends
The European Medicines Agency’s (EMA) advisory committee the CHMP has adopted a positive opinion for a label update of Danish ...
The Pharma Letter
1 天
Takeda‘s Fruzaqla wins UK approval for CRC
The UK’s MHRA has approved Takeda’s Fruzaqla (fruquintinib) for metastatic colorectal cancer (CRC) in adults who have not ...
The Pharma Letter
1 天
Novo Nordisk’s obesity newcomer monlunabant heads into Phase IIb
Novo Nordisk has announced positive Phase IIa results for monlunabant, a small molecule oral CB1 inverse agonist for obesity.
The Pharma Letter
1 天
Latest batch of EMA’s human medicines committee recommendations
Committee for Human Medicinal Products (CHMP) recommended approval of five novel medicines at its September meeting ...
The Pharma Letter
1 天
How biopharma companies can make the best choices
Leslie Orne, president and CEO of Trinity Life Sciences, emphasizes the importance of corporate efficiency in the highly ...
The Pharma Letter
1 天
Phase III win for tolebrutinib in progressive multiple sclerosis
Sanofi has reported positive results from its Phase III HERCULES trial of tolebrutinib for non-relapsing secondary ...
The Pharma Letter
1 天
BioXcel announces new priorities
BioXcel Therapeutics has announced a clinical reprioritization, focusing on late-stage development of its agitation treatment ...
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