Data Points to Potential for Patient Centricity in Rare Disease Trial Success
For health policymakers at a national level, rare diseases are those affecting a tiny fraction of the population. Worldwide, however, this…
For health policymakers at a national level, rare diseases are those affecting a tiny fraction of the population. Worldwide, however, this…
The healthcare landscape faces turbulent times. Regulatory pressures, challenges around demand forecasting and an influx of novel therapies are heaping…
Pediatric clinical trials are often designed according to templates established for adults. Yet there are notable differences between adults and…
The evolving mRNA landscape has been marked by rapid advancements and a broadening scope of applications, primarily driven by the…
Cell and gene therapies represent a groundbreaking advancement in medical science, offering transformative opportunities for treating complex and previously untreatable…
A recent survey for GlobalData’s “State of the Biopharmaceutical Industry 2025” report, conducted at the end of 2024, found drug…
The obesity therapeutics market has gone from a standing start to the story of the year in biopharmaceuticals - and…
Reducing patient burden in clinical trials – especially for rare diseases – is a key objective for drug developers. Decentralized…
Developing treatments for rare diseases, known as orphan drugs, presents a range of unique challenges from the outset, from limited…
Cell and gene therapies (CGTs) are currently at the heart of dynamic trends in the pharma sector. While oncology remains…