Pharma Monthly – December 2025
December 2025 wrapped up the year with a wave of clinical progress, strategic licensing deals, and investment shifts across the pharma and biotech landscape. Leading companies pursued next-generation therapies in oncology, immunology, and gene editing, while M&A activity and pipeline partnerships continued to reshape portfolios.
FDA approval of the drug in combination with Perjeta initiates a $150 million milestone payment to Daiichi Sankyo from AstraZeneca under their joint collaboration.
The deal adds early-stage candidates for breast, lung, and other tumour types, using RIPTAC technology, to J&J’s pipeline.
Johnson & Johnson has received European Commission approval for nipocalimab, marketed as IMAAVY, as an add-on therapy for generalised myasthenia gravis (gMG).
Eli Lilly and Indiana University (IU) have announced a new agreement, under which Lilly will provide up to $40m to IU in order to expand access to clinical trials in Indiana.
Eli Lilly has announced new study data on Inluriyo (imlunestrant) as a treatment for patients with ER+, HER2– metastatic breast cancer.
Lilly has announced plans to build a $6bn facility in Alabama in the US for the manufacture of active pharmaceutical ingredients (APIs).
Moderna is seeking to enhance some of its drugs with Nanexa’s technology as the biologics sector moves to less frequent dosing.
This discovery deal falls under Novartis’ wider ploy to strengthen its immunology portfolio.
The impurities research illustrates an approach that could offer a simpler and more flexible downstream purification process.
Novo Nordisk has presented new findings from its phase 3 Evoke and Evoke+ trials on using semaglutide as part of Alzheimer’s disease (AD) treatment.
This comes just under a month after Pfizer finalised a deal to acquire Metsera following a bidding war with Novo Nordisk.
The cuts follow a broader downgrading of the drug manufacturer’s Swiss operations.
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The in vivo, one-time gene editing therapy has potential to transform outcomes for alpha-1 antitrypsin deficiency (AATD).
Sanofi is adding a hepatitis B vaccine and shingles vaccine candidate to its portfolio via the deal.
Sanofi has agreed $1.7bn and $1.04bn licensing deals with Dren Bio and ADEL, respectively.
The $11bn collaboration with the Chinese biopharma company gives Takeda the rights to several next-generation candidates.
The deal is anticipated to be finalised in the first quarter of 2026, pending the fulfilment of all closing conditions.
Macro Developments
Researchers at the University of Geneva (UNIGE) have developed in vitro models of the kidneys, liver and heart for the purposes of testing the effects of new cancer treatments on healthy tissue
The UK and US have agreed to keep tariffs on UK pharmaceutical shipments into the US at zero.
And as the Critical Medicines Act advances, so too does the Biotech Act, with the moves attracting mixed support from the region’s pharma industry.
New phase I data suggests the oral small molecule ASC50 could help address immunology conditions such as psoriasis.
New BSI standard PAS 2090 could reshape how the pharmaceutical industry reports and minimises its environmental footprint.