BioWorld. Link to homepage.
BioWorld
BioWorld MedTech
BioWorld Asia
BioWorld Science
Data Snapshots
BioWorld
BioWorld MedTech
Infographics: Dynamic digital data analysis
Index insights
NME Digest
Special reports
Infographics: Dynamic digital data analysis
Trump administration impacts
Under threat: mRNA vaccine research
BioWorld at 35
Biopharma M&A scorecard
BioWorld 2024 review
BioWorld MedTech 2024 review
BioWorld Science 2024 review
Women's health
China's GLP-1 landscape
PFA re-energizes afib market
China CAR T
Alzheimer's disease
Coronavirus
More reports can be found here
BioWorld. Link to homepage.
Sign In
Sign Out
My Account
Subscribe
BioWorld - Sunday, December 7, 2025
Home
»
Newsletters
» BioWorld Science
BioWorld Science
Dec. 24, 2013
View Archived Issues
EZH2 inhibition as a promising approach for treating CML
Read More
Discovery of a BTK inhibitor for the treatment of lupus-related renal disease
Read More
Amarantus expands intellectual property portfolio for MANF
Read More
Perrigo's acquisition of Elan Corporation completed
Read More
America Stem Cell changes name
Read More
Ivy Foundation awards grant to support brain cancer research
Read More
FDA grants orphan drug status to metadoxine in fragile X syndrome
Read More
Pleiotropic pathway modulator CC-122 evaluated in first-in-human trial
Read More
MAPK 14 inhibitor devised for use as a CNS probe
Read More
Chinese group presents new S1P1 receptor ligands
Read More
Researchers at Bayer Schering Pharma disclose new GLUT1 inhibitors for cancer
Read More
Novel tankyrase inhibitors synthesized by Roche
Read More
Novel BACE1 inhibitors for Alzheimer's disease reported by Lundbeck
Read More
Astex Therapeutics patents novel FGFR inhibitors
Read More
BioCryst submits NDA for peramivir to treat influenza
Read More
Pozen to conduct comparative pharmacokinetic study of PA-8140/PA-32540
Read More
Eli Lilly and Boehringer Ingelheim submit NDA to FDA for new insulin glargine product
Read More
Auxilium Pharmaceuticals submits supplemental BLA to the FDA for Xiaflex
Read More
EMA accepts filing of MAA for cangrelor
Read More
Regulatory application filed for nivolumab in malignant melanoma
Read More
Tretten approved in the U.S. for congenital FXIII A-subunit deficiency
Read More
Tafenoquine obtains FDA breakthrough therapy designation
Read More
Cervarix two-dose schedule receives European marketing authorization
Read More
EMA accepts dalbavancin MAA for review
Read More
FDA approves Orenitram for PAH
Read More
Actelion's Opsumit granted marketing authorization in the E.U. for PAH
Read More