Pharmaceutical

The ‘Hispanic Paradox’ intrigues a new generation of re...

With better data, powerful genomic tools, and a rich cultural awareness of the c...

STAT+: Civica Rx considers moving into chemo drugs as s...

A hospital nonprofit formed to deal with drug shortages, Civica Rx, is consideri...

Novelist John Green launches attack on Cepheid over the...

John Green, a novelist and popular YouTuber, is once again leveraging his star p...

Opinion: Long Covid is a new name for an old syndrome

Although much about ME/CFS is still not well-understood, decades of experience a...

STAT+: FDA panel endorses Alnylam’s heart drug — after ...

“It’s like a light wind blowing in favor of patisiran over placebo,” said David ...

STAT+: What to make of Biden’s latest Cancer Moonshot e...

President Biden’s latest Cancer Moonshot efforts are inspiring hope among cancer...

STAT+: Akili abandons prescription business model, to l...

Akili's move from prescription to OTC sales for its ADHD therapy signifies a maj...

STAT+: Lawmakers introduce bill to require drugmakers t...

A new bill seeks to have the FDA and the U.S. Patent Office coordinate efforts t...

STAT+: In new Regeneron deal for Covid drug, White Hous...

A groundbreaking clause in a deal between the Department of Health and Human Ser...

Menarini signs agreement for Astellas’s rheumatoid arth...

Menarini Asia-Pacific has entered a long-term exclusive agreement to license Ast...

Dewpoint and Chemify partner for cancer drug discovery

Dewpoint Therapeutics entered a collaboration with Chemify to expedite the disco...

Avalo drops three rare disease assets amid ongoing chal...

The company will divest the AVTX-800 rare disease compound series to AUG Therape...

Results from Rybrevant trial solidify Janssen’s foothol...

Currently, NSCLC patients with EGFR exon 19 deletions or L858R substitution face...

Bristol Myers Squibb’s Reblozyl reinforces market share...

On August 28, the FDA approved the label expansion of Bristol Myers Squibb’s Reb...

FDA to start review of subcutaneous Entyvio for Crohn’s...

The FDA is also reviewing a subcutaneous formulation of Takeda’s blockbuster dru...

FDA calls out eight companies for selling unapproved ey...

The US Food and Drug Administration has sent letters to eight companies for unau...