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APPROVALS

ViiV initiates rolling submission of NDA for injectable PrEP in US
APPROVALS

ViiV initiates rolling submission of NDA for injectable PrEP in US

Dominic Cuthbert -
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Farxiga approved in the US for the treatment of chronic kidney disease
APPROVALS

Farxiga approved in the US for the treatment of chronic kidney disease

Dominic Cuthbert -
0
WHO issues Emergency Use Listing for Moderna’s COVID vaccine
APPROVALS

WHO issues Emergency Use Listing for Moderna’s COVID vaccine

Dominic Cuthbert -
0
Jemperli becomes first anti-PD-1 therapy available for endometrial cancer in Europe
APPROVALS

Jemperli becomes first anti-PD-1 therapy available for endometrial cancer in Europe

Dominic Cuthbert -
0
FDA accepts Airway’s IND to develop novel recombinant protein for COVID-19
APPROVALS

FDA accepts Airway’s IND to develop novel recombinant protein for COVID-19

Dominic Cuthbert -
0
FDA allows SPI to test ebselen as novel COVID-19 treatment
APPROVALS

FDA allows SPI to test ebselen as novel COVID-19 treatment

Dominic Cuthbert -
0
US approves PONVORY for relapsing multiple sclerosis
APPROVALS

US approves PONVORY for relapsing multiple sclerosis

Dominic Cuthbert -
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CDC Advisory Committee recommends first single-shot COVID-19 vaccine for US adults
APPROVALS

CDC Advisory Committee recommends first single-shot COVID-19 vaccine for US adults

Dominic Cuthbert -
0
Lilly’s bamlanivimab-etesevimab combo granted emergency use for COVID-19
APPROVALS

Lilly’s bamlanivimab-etesevimab combo granted emergency use for COVID-19

Dominic Cuthbert -
0
ViiV secures European marketing authorisation for fostemsavir
APPROVALS

ViiV secures European marketing authorisation for fostemsavir

Dominic Cuthbert -
0
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