Eli Lilly and Company has received approval from the US FDA for the expanded use of Jaypirca tablets in 100mg and 50mg doses.

If Richard Padzur retires, he would become one of several high-ranking FDA officials who left the agency in 2025.

On 1 December, the fortunes of the UK pharma sector changed radically, with the UK Government becoming the first in the world ...

AGC Biologics is set to expand its Cell Line Development Centre of Excellence through a partnership with ATUM.

Citizen Health has entered a multi-year strategic partnership with UCB for expediting drug development across five rare ...

New non-primate draft guidance follows the FDA's wider aim to curtail the use of animal testing in preclinical toxicology.

The World Health Organization (WHO) predicts that fewer than 10% of eligible patients will have access to GLP-1RAs by 2030.

Rare disease research faces complex regulations, small patient populations, and high costs. As traditional incentives wane, ...

Patient advocacy and industry bodies welcomed the bill’s backing, though it will now need to be passed in the Senate.

Biotechs in the charter city of Próspera aim to cure ageing, but experts question the feasibility of their goals.

Data management in oncology clinical trials features multiple complexities, and choosing the right EDC system is essential.

Solid Biosciences has secured US FDA rare paediatric disease designation for SGT-212, its investigational gene therapy targeting FA.