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The Pharma Letter
23 小时
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
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
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
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
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
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
3 天
Helsinn Pharmaceuticals
A fully integrated global biopharma company headquartered in Lugano, Switzerland. It is focused on improving the lives of cancer patients all over the world with a leading position in cancer ...
The Pharma Letter
3 天
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39-43 Putney High Street, Putney London, SW15 1SP United Kingdom ...
The Pharma Letter
3 天
AstraZeneca withdraws EU submission for lung cancer drug
AstraZeneca and Daiichi Sankyo withdraw EU application for datopotamab deruxtecan in NSCLC after Phase III trial shows no ...
The Pharma Letter
3 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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