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GSK plc (GSK) Presents at Goldman Sachs 9th Annual Biopharma Innovation Summit Transcript
Shore Capital has reiterated its buy recommendation on GSK PLC (LSE:GSK, NYSE:GSK) with a fair value of 2,500p, arguing the pharmaceutical group's shares are too cheap given the scale of its growth ambitions and that two of the market's main concerns about the business are beginning to fade. The broker's analyst, Dr Sean Conroy, said GSK, which has a market capitalisation of around £79 billion, trades at 14 times his 2026 earnings estimate and 12 times his 2027 forecast, a level he described as undemanding relative to peers on comparable growth.
GSK secures Japan orphan drug status for risvutatug rezetecan in SCLC, adding to multiple global designations backed by promising early data.
Wondering how to pick strong, market-beating stocks for your investment portfolio? Look no further than the Zacks Style Scores.
The U.S. Food and Drug Administration approved GSK's drug for severe relentless itching caused by a type of liver disease, the company said on Thursday, making it the first treatment greenlit for the condition.
GSK, with Luke Miels becoming its new CEO in early 2026, continues its successful expansion into the oncology and cardiovascular drugs markets. So, on February 25, GSK announced that it acquired 35Pharma for $950 million, which, in turn, is developing HS235 for the treatment of pulmonary hypertension. Moreover, the performance of its HIV blockbuster, Dovato, also did not disappoint me.
GSK and Amgen will add their medicines to TrumpRX, the prescription drug website launched by President Donald Trump's administration, Fox Business reported on Friday.
British drugmaker GSK said on Friday the U.S. Food and Drug Administration has expanded the approved age range for its respiratory syncytial virus vaccine, Arexvy, to include adults aged 18 to 49 who are at increased risk of lower respiratory tract disease caused by the virus.
GSK plc (GSK) Presents at Barclays 28th Annual Global Healthcare Conference Transcript
GSK licenses linerixibat to Alfasigma for cholestatic pruritus in PBC, securing $300M upfront and potential milestone payments as the drug awaits FDA review.
The British pharma giant will hand off its experimental itch treatment to Italian company Alfasigma as it focuses on broader liver disease pipeline GSK PLC (LSE:GSK, NYSE:GSK), the British pharmaceutical giant, has agreed to license worldwide rights to its experimental liver disease drug linerixibat to Italian pharma company Alfasigma in a deal worth up to $690 million. Under the terms of the agreement, GSK will receive an upfront payment of $300 million, a further $100 million upon US Food and Drug Administration (FDA) approval, $20 million on EU and UK approval, and up to $270 million in sales-based milestone payments, as well as tiered double-digit royalties on net sales.