
Where do Stem Cells Fit in the Future of Medicine?
In recent weeks, we have issued reports highlighting cell and gene therapy from various perspectives. Another area of research under the same umbrella is stem

In recent weeks, we have issued reports highlighting cell and gene therapy from various perspectives. Another area of research under the same umbrella is stem

Today our spotlight is on how well a gene therapy approved in early 2024 has performed with a lookback at several years preapproval and over

A fog of uncertainty hangs thickly in the air. Manufacturers find themselves wringing their hands in the aftermath of sweeping layoffs and shifting policies at

Orphan Drugs are significantly impacting the health care market. A recent independent report analyzes the key market elements and challenges, providing some guidance to pharmaceutical

The FDA recently approved a new indication for an infused therapy, Uplizna (inebilizumab-cdon) from Amgen. While the therapy was originally approved in 2020, this approval

Earlier this week, we delved into the topic of Accelerated Approval Pathways and the critical role played by surrogate endpoints. Today, let’s delve even deeper

Quiz me this……….What is a surrogate endpoint, and what the heck do they have to do with a drug obtaining Accelerated Approval? People working in

Global Pharma industry has been buzzing about the looming tariffs from the US being applied for everything from Hello Kitty chotchkie to, ‘say it ain’t

A recent Executive Order directing HHS to develop price targets for imported drugs has really stirred up the hornet’s nest. It is common knowledge that

The FDA recently approved a new treatment, Qfitlia (fitusiran) from Sanofi, for routine prophylaxis to prevent or reduce the frequency of bleeding episodes in adult
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