UK relies on EMA’s review of Xgeva reformulation in first-ever reciprocal approval
For the first time since Brexit, the UK’s medicines regulator has made use of its new approval pathway that can speed drug approvals based on
For the first time since Brexit, the UK’s medicines regulator has made use of its new approval pathway that can speed drug approvals based on
A federal judge in Delaware on Friday ruled in favor of the Biden administration in a case brought by AstraZeneca seeking to overturn parts of
Moderna has made cuts at its Burlington and Norwood sites in Massachusetts, a spokesperson confirmed to Endpoints News, including some workers in quality assurance. “Moderna previously
Plus, news about Tarsus Pharmaceuticals, Humacyte, Stemcell Technologies and SQZ Biotechnologies: Achieve Life Sciences raises $124M, details plans for NDA: The company plans to submit
In a bid to overcome some of the commercial challenges faced by expensive new gene therapies, Quantile Health has raised $6 million for a financial
FogPharma, a biotech from Harvard researcher Greg Verdine that is led by former Johnson & Johnson R&D leader Mathai Mammen, said it has raised $145
(This story is from our new Health Tech newsletter. If you’d like to sign up, just click here.) As weight loss drugs boom in popularity,
Share this article The diagnostic industry is growing and evolving – picking the right partnerships can help with the process of navigating change. Credit: Mongkolchon
WASHINGTON — Although FDA approval has eluded the intranasal epinephrine spray ARS-1 (also known as neffy), it continued to build its case with findings of
More than 90% of patients with locally advanced basal cell carcinoma (BCC) of the head and neck achieved locoregional control (LRC) with vismodegib (Erivedge) and