The CHMP renders a positive opinion recommending approval for MRK's Keytruda for the first-line treatment of malignant ...
The European Union health agency on Monday warned that Europe was set to miss goals on reducing the use of antibiotics, ...
The EC has approved Elahere for treating adult patients with folate receptor-alpha (FRα) positive, platinum-resistant and ...
That Thursday, for the first time, the European Medicines Agency (EMA) approved a drug that targets the cause — not just the ...
NORTH CHICAGO, IL, USA I 18, 2024 I AbbVie (NYSE: ABBV) today announced the European Commission (EC) granted marketing authorization for ELAHERE® ...
The New Drug Application is based on positive results from the Phase 3 PALISADE study – People living with familial chylomicronemia syndrome have extremely high triglyceride ...
The study showed significant reductions in serum TTR levels in subjects after a single dose, with sustained effects over time ...
Committee for Medicinal Products for Human Use (CHMP) has recommended the approval of a combination therapy consisting of ...
(RTTNews) - Janssen-Cilag International NV, a Johnson & Johnson company (JNJ), Monday said that the European Medicines Agency's Committee for Medicinal Products for Human Use (CHMP) has recommended ...
A new study reveals that more than half of cancer drugs approved by the FDA under accelerated pathways are not authorized in ...
InflaRx (IFRX) has released an update. InflaRx has received a positive opinion from the European Medicines Agency’s CHMP for GOHIBIC, a ...
Patients with MSI-high/dMMR advanced colorectal cancers had a 79 percent lower risk of disease progression or death on Opdivo-Yervoy compared to chemo.