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Priority review sets up Feb verdict on Sanofi, Sobi haemophi...

The FDA will carry out a speedy review of Sanofi and Sobi's once-weekly haemophilia A treatment efanesoctocog alfa (Bivv001), with a decision now

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Red blood cells moving in blood vessels with depth of field.

Sanofi trumpets data with haemophilia treatment duo at ISTH

Sanofi R&D in its core haemophilia category is advancing on three fronts – engineered proteins, RNA interference drugs and gene therapies – and highlighted results in two of those at th

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Sobi bolsters blood division via $435m ADC licensing deal

Swedish rare disease specialist Sobi is paying $55 million upfront to license rights to ADC Therapeutics' lymphoma therapy Zynlonta – approved in the US last year – in Europe and other inte

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Alnylam grabs FDA approval for its second amyloidosis therap...

Four years after getting the first drug approved by the FDA to treat rare disease hereditary ATTR amyloidosis, Alnylam has got the go-ahead for a second – Amvuttra – which has a simpler, mo

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Sanofi, Sobi eye filings for once-weekly haemophilia A thera...

Sanofi and Sobi's haemophilia partnership has been under competitive pressure from new therapies like Roche's antibody Hemlibra, so the two companies are hoping a new long-acting drug candi

News

After GSK stumble, Pfizer moves forward with RSV vaccine

Pfizer has been awarded breakthrough status from the FDA for its respiratory syncytial virus (RSV) vaccine in pregnant women, putting the company in pole position to bring a shot to market

Priority review sets up Feb verdict on Sanofi, Sobi haemophi...

Sanofi trumpets data with haemophilia treatment duo at ISTH

Sobi bolsters blood division via $435m ADC licensing deal

Alnylam grabs FDA approval for its second amyloidosis therap...

Sanofi, Sobi eye filings for once-weekly haemophilia A thera...

After GSK stumble, Pfizer moves forward with RSV vaccine

FDA experts lukewarm on AZ's anticoagulant antidote Andexxa

Coming soon: The Life Sciences Industry Report 2025 – insigh...

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