Zasocitinib is also being evaluated in a head-to-head study against Bristol Myers Squibb’s Sotyktu (deucravacitinib) in ...
Eli Lilly has now submitted a new drug application (NDA) for GLP-1RA orforglipron to the FDA for use in adults with obesity.
Shares in Tokyo-listed Nxera Pharma slid 5% at market open after Boehringer walked away from the neurological assets.
Transforming US drug access and production: MFN pricing deals and historic manufacturing investments
In November 2025, US President Donald Trump announced transformative actions to lower prescription drug costs and secure the ...
J&J has received the US FDA approval for Rybrevant Faspro, a SC administered therapy to treat patients with EGFR-mutated ...
The MHRA has launched a call for evidence seeking input from healthcare providers, the public, and health experts on AI ...
The EC has approved Incyte’s Minjuvi (tafasitamab) with lenalidomide and rituximab for adults with relapsed or refractory FL.
Poised to become law, the BIOSECURE Act will have ramifications for certain US-China pharmaceutical relationships.
Targeted patient recruitment can increase the likelihood of trial success and help cultivate use of precision medicine.
INCOG BioPharma Services has announced an injectable drug manufacturing expansion at its Fishers facility in Indiana, US.
Propelled by a flurry of dealmaking late in the year, 2025 M&A ended on a strong note, with high activity expected to ...
The US Food and Drug Administration has approved Acadia Pharmaceuticals’ Daybue Stix (trofinetide), a dye and ...
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