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The Pharma Letter
21 小时
FDA approves new injectable version of Opdivo
The US Food and Drug Administration (FDA) on Friday approved nivolumab and hyaluronidase-nvhy, under the trade name Opdivo ...
The Pharma Letter
1 天
Akums in long-term deal to supply oral drugs to Europe
Akums secures a strategic deal to manufacture and supply oral liquid formulations for a global pharma company in Europe. The ...
The Pharma Letter
1 天
Second FDA approval for BeiGene’s Tevimbra in 2024
The US Food and Drug Administration (FDA) has approved Tevimbra (tislelizumab-jsgr), in combination with platinum and ...
The Pharma Letter
1 天
Inmagene takes back-door route to Nasdaq listing
Inmagene Biopharmaceuticals merges with Ikena Oncology to form InmageneBio, focusing on IMG-007, an OX40-targeting antibody ...
The Pharma Letter
1 天
AusperBio raises $73 million to advance hepatitis B therapy
AusperBio raises $73 million in series B funding to advance Phase II trials of AHB-137, its antisense oligonucleotide therapy ...
The Pharma Letter
1 天
Mankind Pharma and Innovent partner for sintilimab
Mumbai, India-based Mankind Pharma has entered into a partnership with China’s Innovent Biologics for exclusively licensing ...
The Pharma Letter
2 天
Takeda’s Hyqvia approved as first-of-kind immunoglobulin therapy in Japan
The Japanese Ministry of Health, Labor and Welfare (MHLW) has approved the use of Hyqvia (immune globulin infusion 10% [human ...
The Pharma Letter
2 天
FDA label changes for transmucosal buprenorphine products
The US Food and Drug Administration (FDA) has issued the Federal Register notice, Modifications to Labeling of ...
The Pharma Letter
1 天
Kaken inks license agreement for STAT6 Inhibitor
Japanese drugmaker Kaken Pharmaceutical has entered into a license agreement with US healthcare giant Johnson & Johnson for ...
The Pharma Letter
5 天
FDA approves Lilly drug for obstructive sleep apnea
US pharma major Eli Lilly today announced the US Food and Drug Administration (FDA) approved Zepbound its (tirzepatide) as ...
The Pharma Letter
5 天
Sumitomo gains FDA approval of Gemtesa for OAB
The US subsidiary of Japan’s Sumitomo Pharma announced that the US Food and Drug Administration (FDA) has approved Gemtesa ...
The Pharma Letter
4 天
Viatris faces FDA import restrictions at Indian facility
Viatris faces US FDA regulatory action on its Indore, India facility, with a warning letter and import alert restricting 11 ...
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