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In Focus channel feed
'Find a way, or make one': How two scientists hope to revitalize CRISPR's rare disease crisis
Yesterday
R&D
Cell/Gene Tx
The inside story of how SalioGen, a startup trying to wrangle ‘jumping genes’ to make medicines, fell apart
Last week
Startups
US drugmakers increasingly look abroad for clinical trials as confidence in FDA wavers
Last week
Pharma
Primate researchers cope with uncertainty as NIH appeals for payment cuts in court
4 weeks ago
R&D
Pharma
‘People will die’: End of NIH grants guts work between academics and companies to counter next pandemic
Last month
R&D
Illumina was built on DNA. Its future could be biology’s next big wave
Last month
Diagnostics
A California health tech company is letting AI run medical visits, from intake to diagnosis
Last month
AI
Health Tech
Ahead of FDA decision, Alnylam faces the big question: Can it make money?
Last month
Pharma
FDA+
Inside NYC’s waitlist-only health tech club, where young professionals find both friends and jobs
Last month
Health Tech
Trump’s science crackdown hits rare disease research: ‘We need to sit down with Elon Musk’
2 months ago
Financing
Can Bill Anderson save Bayer?
2 months ago
People
Pharma
Will CRISPR matter?
2 months ago
R&D
Special
Drugmakers seize on biomarkers to test the FDA's rare disease shift
3 months ago
R&D
FDA+
Trump blog: Federal agencies must give jobs back to fired probationary workers, judge rules
3 months ago
Pharma
FDA+
China's biotech boom is threatening US drugmakers' dominance
3 months ago
R&D
China
Broad Institute paper offers potential new framework for treating Huntington’s disease
3 months ago
R&D
How a duty to spend wisely on worker benefits could loosen PBMs' grip on drug prices
4 months ago
Pharma
Law
Inside Isomorphic Labs: Demis Hassabis’ lab-free vision for biotech’s AI future
4 months ago
AI
As 23andMe struggles, another genetic testing company bets on drug discovery
5 months ago
R&D
Discovery
Lawmakers are poking holes in pharma's favorite new way to market medicines
5 months ago
Pharma
Health Tech
A rare neurological disease is Sage’s last, best hope after failures in depression
5 months ago
R&D
Pharma
Yorvipath’s approval showcases biopharma’s interest in rare endocrine disorder
5 months ago
Startups
R&D
Biotech industry worries over potential for RFK Jr. ally as FDA pick
6 months ago
FDA+
Is there room for MASH drugs in a GLP-1 world?
6 months ago
R&D
Pharma
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