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EC Authorizes Opdualag From BMS As A Melanoma Treatment

The fixed-dose combination Opdualag (nivolumab and relatlimab) from Bristol Myers Squibb (BMS) has received clearance from the European Commission for use as the first-line...

GAVI Funds To Enable Quick Finances For The Next Pandemic

According to Chief Executive Seth Berkley of the global vaccination alliance GAVI, the organisation has set up financial structures that would enable it to...

Bluebird Hits $3m Mark With Gene Therapy After FDA Approval

Within one firm, the title of most costly treatment in the world has changed hands within a month. Bluebird Bio has received an FDA fast...

First Next-Gen Parkinsons Med To Be Made By Neuron23, QIAGEN

QIAGEN and Neuron23TM Inc., an early-stage biotechnology company focused on creating precision medications for genetically defined neurological and immunological illnesses, have announced a partnership...

Australia Permits New Treatment For Rare Bile Duct Cancer

Australia has authorised the use of a new targeted therapy for the treatment of cholangiocarcinoma, a rare bile duct cancer. The Therapeutic Goods Administration...

Beyfortus From Sanofi And Astrazeneca Is Supported By RSV

Beyfortus has received approval from the Committee for Medicinal Products for Human Use (CHMP) of the European Medicines Agency to treat lower respiratory tract...

canSERV, EU Cluster Effort, Offers Cancer Study In Europe

Brussels marks the beginning of the European canSERV initiative, which aims to defragment the European cancer research landscape. CanSERV will give academia and business...

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