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The Pharma Letter
New data for GSK’s Arexvy RSV vaccine | Pharmaceutical | The Phar…
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The Pharma Letter
Merck’s clesrovimab shows promise for RSV prevention in infants | Biotechno…
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The Pharma Letter
Pfizer to help commercialize Xacduro in China | Pharmaceutical | The Pharm…
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The Pharma Letter
BeiGene's Tevimbra gains approval in Israel | Biotechnology | The Pharmal…
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The Pharma Letter
Inify secures $12.3 million, plans UK expansion | Pharmaceutical | The Ph…
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The Pharma Letter
Moderna's rare disease candidate selected for US FDA's START progra…
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The Pharma Letter
RAPT Thera ends zelnecirnon program after FDA worries | Biotechnology | T…
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The Pharma Letter
Lilly and Innovent to commercialize Jaypirca in China | Pharmaceutical | …
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The Pharma Letter
South Korea’s GC Biopharma partners with Novelty Nobility | Biotechnology …
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The Pharma Letter
Atara Therapeutics appoints Cokey Nguyen as chief executive | Biotechn…
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The Pharma Letter
Accord acquires Coherus’ Udenyca business | Biosimilars | The Pharmal…
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The Pharma Letter
Argenx and Zai Lab secure China approval for Vyvgart Hytrulo | Biotech…
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The Pharma Letter
Surprise third quarter profit as Moderna affirms guidance | Biotechnology | Th…
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The Pharma Letter
Transgene cancer vaccine TG4001 trial misses main goal | Biotechnology | T…
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The Pharma Letter
Semglee success to spur pricing pressure in US insulin market | Biosi…
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The Pharma Letter
AAIC 2024: long-term Leqembi use safe and effective | Biotechnology | T…
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The Pharma Letter
FDA panel flags risks as AstraZeneca seeks full Andexxa approval | Biotech…
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The Pharma Letter
FDA sets up Rare Diseases Innovation Hub | Pharmaceutical | The Pharmal…
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The Pharma Letter
New Amgen med shows benefit in treating uncontrolled gout | Biotechno…
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The Pharma Letter
ASCO 22: Promising early data for next-gen CAR T-cell therapy | Biotec…
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The Pharma Letter
Novartis oral Fabhalta win in Phase III C3 glomerulopathy trial | Pharmaceut…
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The Pharma Letter
Mid-stage data advance Adaptimmune’s cell therapy pipeline …
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The Pharma Letter
Another approval for Bausch Health's new glaucoma treatment | Pharmace…
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The Pharma Letter
Gilead strengthens seladelpar case in PBC | Pharmaceutical | The Pharmal…
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The Pharma Letter
MHRA approves Filspari for IgAN | The Pharmaletter
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The Pharma Letter
EC approves Astellas’ Padcev for added indication | Pharmaceutical | T…
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The Pharma Letter
UK approves new Comirnaty jab targeting latest subvariant | Biotechn…
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The Pharma Letter
Santhera secures first DMD approval in China | Pharmaceutical | The Pharm…
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The Pharma Letter
Teva and Daiichi Sankyo named and shamed for UK code breaches | Phar…
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The Pharma Letter
Early UK access to Jemperli in endometrial cancer setting | Biotechno…
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The Pharma Letter
Citius to spin off oncology division into separate public company | Biotechnol…
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The Pharma Letter
Kyle Gano to lead Neurocrine in post-Kevin Gorman era | Pharmac…
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The Pharma Letter
StemCyte gains FDA nod for cord blood therapy | Biotechnology | The Pharmaletter | The Pharmaletter
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The Pharma Letter
Indian pharma sees surge in US inquiries amid Biosecure Act talks | Pharmaceutical | The ...
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Biogen and Sage share more on zuranolone Phase III PPD trial | Biotechnology | The Pharmaletter ...
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