Turning bottlenecks into breakthroughs in gene therapy manufacturing
In late 2023, the first CRISPR-based gene therapy for sickle cell disease patients Casgevy, received the seal of approval from…
In late 2023, the first CRISPR-based gene therapy for sickle cell disease patients Casgevy, received the seal of approval from…
ADCs are precision medicines that hitch a cell-killing drug (the “payload”) to an antibody via a chemical “linker”. The antibody…
GlobalData estimates suggest that, across seven of the world’s major pharmaceutical markets - the US, the big five in Europe…
Developing oncology medications is a complicated and costly process. While clinical trial designs have improved, these trials still face difficulties…
Biopharma innovators are operating in an environment shaped by the medical need for new and advanced therapies, the sheer volume…
Few industries have innovated more prodigiously than biopharma over recent years. But its adoption of digital innovations has lagged. Today,…
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…