Pharmaceutical

Excitement associated with FDA approval of Rinvoq in Cr...

Rinvoq is expected to have a rapid uptake in the CD market by healthcare provide...

Daiichi Sankyo receives Japan’s MHLW approval for VANFLYTA

VANFLYTA was first approved as a monotherapy in the relapsed/refractory setting.

FDA grants priority review for Takeda and HUTCHMED’s fr...

The NDA included data from the Phase III FRESCO-2 and FRESCO trials conducted in...

FDA awards full approval to Paxlovid amidst hazy covera...

A few weeks after Covid-19 emergency declaration ended, the FDA has approved Pax...

Immuno-oncology market set to grow in billions, but acc...

The immune-oncology market is forecasted to grow to over $150 billion by 2028, b...

Touchlight boosts DNA manufacturing capacity with lates...

The larger facility is expected to help Touchlight supply plasmid DNA to meet th...

Beta Bionics’ automated insulin delivery system picks u...

Insulin delivery devices are proliferating despite equitable insulin access bein...

Illegal online pharmacies gain traction as regulators l...

As US drug prices increase, consumers are turning to illegal online pharmacies t...

Krystal Biotech receives FDA approval for DEB topical g...

Patients with DEB have extremely fragile skin that blisters and tears with minor...

STAT+: U.K. unveils $800 million package to bolster lif...

The U.K. government on Thursday unveiled an $800 million package to bolster the ...

STAT+: Bristol drug reduces reliance on transfusions fo...

In a new study, a medicine from Bristol Myers Squibb nearly doubled the treatmen...

STAT+: Gilead and Teva defend antitrust claims that pri...

“We’ve lost an opportunity to have direct government purchases of hundreds of th...

Listen: ChatGPT in medicine, a boom in weight loss pill...

Can AI diagnose a disease? Are Wegovy's days numbered? And what makes AI halluci...

STAT+: Illumina shareholders elect one Icahn ally to bo...

Illumina shareholders elect one of Carl Icahn's allies to board, but the company...

STAT+: Pharmalittle: FDA approvals will stop if U.S. de...

The FDA delayed its decision on a gene therapy for Duchenne muscular dystrophy a...

Opinion: Adopting the term ‘preaddiction’ would be a se...

Adopting the term "preaddiction" could have potentially disastrous consequences ...