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PMLiVE
1 天
ICR researchers uncover new method for predicting bowel cancer risk in IBD patients
Scientists from the Institute of Cancer Research (ICR) have found a new method for predicting bowel cancer risk in ...
PMLiVE
1 天
Amgen’s Blincyto granted EC approval for new acute lymphoblastic leukaemia indication
Amgen’s Blincyto (blinatumomab) has been approved by the European Commission (EC) to treat certain acute lymphoblastic ...
PMLiVE
1 天
NICE approves Vertex’s Casgevy one-time gene therapy for sickle cell disease
The National Institute for Health and Care Excellence (NICE) has approved Vertex Pharmaceuticals’ Casgevy (exagamglogene ...
PMLiVE
1 天
Keto, CAR-T and creativity: insights from ASH 2024
With a menu featuring everything from cutting-edge science to DEI and diet, ASH 2024 certainly offered congress attendees ...
PMLiVE
2 天
Roche shares overall survival results for Itovebi in advanced breast cancer
Levi Garraway, Roche’s chief medical officer and head of global product development, said: “The INAVO120 overall survival ...
PMLiVE
3 天
Novo Nordisk’s Ozempic granted FDA approval in chronic kidney disease
Novo Nordisk’s Ozempic (semaglutide) has been approved by the US Food and Drug Administration (FDA) to reduce the risk of ...
PMLiVE
3 天
Bayer UK launches digital educational hub to improve menopause support
Bayer Consumer Health has launched a digital educational resource to support perimenopausal or menopausal patients in the UK.
PMLiVE
5 天
Havas Health Network launches Havas Life London
Havas Health Network has launched Havas Life London, an evolution of Havas Life Medicom that is “deeply rooted” in the agency ...
PMLiVE
4 天
The silent treatment – researching gene silencing for Alzheimer’s, Parkinson’s and ...
In trials at University College London Hospitals (UCLH), an ASO is being used to target the mutated gene that results in the ...
PMLiVE
3 天
Biogen’s higher dose spinal muscular atrophy regimen accepted for review by EMA/FDA
Biogen has announced that the European Medicines Agency (EMA) and US Food and Drug Administration (FDA) have started ...
PMLiVE
2 天
Sanofi’s Sarclisa combination approved by MHRA for newly diagnosed multiple myeloma
Sanofi’s Sarclisa (isatuximab) has been approved by the Medicines and Healthcare product Regulatory Agency (MHRA) as part of a combination treatment for newly diagnosed multiple myeloma (MM).
PMLiVE
5 天
Biogen/Eisai’s Alzheimer’s drug approved by FDA for monthly maintenance dosing
Biogen and Eisai’s Alzheimer’s disease (AD) drug Leqembi (lecanemab-irmb) has been approved by the US Food and Drug ...
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