Merz Wins Appeal to Block Generic MS Drug Sales in France
Pharmaceutical company Merz has secured a key legal victory in its ongoing dispute over its multiple sclerosis drug Fampyra. The Court of Appeal of the Unified Patent Court (UPC) has overturned an earlier decision and granted a preliminary injunction against Viatris.
Federal Judge Rules North Dakota Drug Access Law Unconstitutional
A federal court in North Dakota has ruled that a state law aimed at expanding access to discounted medications is unconstitutional.
Boehringer Ingelheim Reports 16.6% Weight Loss in Late-Stage Trial of Obesity Drug
In a recent development, Boehringer Ingelheim announced that its experimental obesity drug survodutide achieved an average weight loss of up to 16.6% in a Phase III clinical trial.
Purdue Pharma Sentenced to $5.5 Billion as Court Clears Path for Opioid Settlement
In a significant development in long-running opioid litigation, Purdue Pharma has been sentenced to pay $5.5 billion in fines and penalties following its 2020 guilty plea in connection with the marketing of its opioid drug, OxyContin.
Breaking: Pfizer settles Vyndamax (tafamidis) suit
It has been confirmed today that Pfizer settled with the final defendant, Hikma Pharmaceuticals.
Jazz Pharmaceuticals' Ziihera wins FDA priority review for first-line gastric cancer use
Jazz Pharmaceuticals has secured priority review from US regulators for an expanded use of its targeted cancer therapy Ziihera, advancing the Dublin-headquartered group's bid to establish the drug as a frontline standard of care in HER2-positive gastric and gastroesophageal cancers — one of the more commercially significant unmet needs in oncology.
Ligand to acquire XOMA Royalty for $739mn in deal that doubles biotech royalty portfolio
Ligand Pharmaceuticals has agreed to acquire XOMA Royalty Corporation in an all-cash deal valued at approximately $739mn, doubling the size of its biotech royalty portfolio and cementing its position as one of the dominant aggregators in a niche corner of the pharmaceutical industry that has attracted growing investor attention.
Catalyst Pharmaceuticals draws Italian buyer interest as US rare disease assets fetch premium
Catalyst Pharmaceuticals, the US rare-disease drug developer, has emerged as a potential acquisition target for Italy's Angelini Pharma, in the latest sign of how aggressively European drugmakers are scouring the US market for commercial-stage assets in orphan indications.
Hikma Pharmaceuticals no longer appears to be challenging the validity of Pfizer’s patent
Update from the Vyndamax (tafamidis) trial: Hikma Pharmaceuticals, the holdout defendant, no longer appears to be challenging the validity of Pfizer’s patent.
Novartis wins EU green light for Rhapsido in chronic urticaria, opening front in oral immunology drugs
Novartis has secured European Commission approval for Rhapsido, its oral chronic skin disease drug, broadening the geographic reach of one of the Swiss group's most strategically significant immunology launches and opening a new front in the increasingly competitive market for oral targeted therapies.
Wall Street downgrades Terns Pharmaceuticals as Merck swoops on $6.7bn cancer drug bet
A wave of analyst downgrades has hit Terns Pharmaceuticals after Merck agreed to acquire the US biotech for $6.7bn, ending one of the most striking small-cap rallies of the past year and underlining the willingness of large pharmaceutical groups to pay heavily for differentiated oncology assets.
Big Pharma names sit on UK panel shaping fallout from US-UK drugs trade pact
Nine of the world's largest pharmaceutical companies have been seated alongside UK government officials on a new oversight committee charged with implementing the US-UK pharmaceuticals trade agreement, in a sign of how heavily the Trump administration's drug pricing reset is reshaping the commercial environment for medicines on both sides of the Atlantic.
BREAKING - Pfizer (PFE) SETTLES Tafamidis suit with two of three defendants
BREAKING - Pfizer (PFE) SETTLES Tafamidis suit with two of three defendants. Key question for analysts - how long will Pfizer’s patent protection last under the settlement? Based on available research, generics could be out of the market until 2033-2035. PFE BBIO ALNY
Eli Lilly strikes $6.3bn deal for Centessa to bolster neuroscience pipeline
Eli Lilly has agreed to acquire Centessa Pharmaceuticals in a deal valued at $6.3bn upfront, as the US drugmaker deepens its push into neuroscience and sleep-related disorders.
Ionis rally raises questions over valuation after strong run
Shares in Ionis Pharmaceuticals have surged more than 150 per cent over the past year, prompting investors to reassess whether further upside remains or if much of the growth story is already priced in.
New catalytic method promises more efficient route to amine synthesis
Researchers at the University of Wisconsin–Madison have developed a method to simplify the formation of carbon–nitrogen (C–N) bonds, a fundamental step in producing amines widely used in pharmaceuticals, agrochemicals and advanced materials.
Branded generics gain ground as drugmakers balance cost and trust
The global market for branded generics is expanding rapidly, reflecting mounting pressure on healthcare systems to contain costs while maintaining patient confidence in treatment quality.
Trump secures final drug pricing accord with Regeneron
US President Donald Trump has announced a pricing agreement with Regeneron Pharmaceuticals, marking the final deal in a series of negotiations between the administration and leading drugmakers aimed at lowering the cost of medicines in the US.
South Korea climbs to third in global drug development pipeline
South Korea has consolidated its position as a leading player in pharmaceutical innovation, ranking third globally for drug development pipelines in 2026, behind only the US and China, according to industry data.
Lilly rejects subsidised listing for diabetes drug amid pricing dispute
Eli Lilly has declined to list its diabetes treatment Mounjaro on Australia’s Pharmaceutical Benefits Scheme (PBS), despite a recommendation from the country’s medicines regulator, citing what it described as an unacceptably low pricing proposal from the federal government.