AML

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FDA grants full approval for Roche/AbbVie's Venclexta in AML...

Combination therapies involving Roche and AbbVie’s cancer drug Venclexta have been formally approved by the FDA in acute myeloid leukaemia, following supportive data from late-stage studies

News

Gilead to buy immuno-oncology firm Forty Seven for $4.9bn

Gilead is to buy immuno-oncology firm Forty Seven for $4.9 billion, adding an antibody targeting several blood cancers to its research pipeline.

News

NICE rejects Astellas' Xospata in AML, queries MSD's Keytrud...

NICE has been busy with announcements today, rejecting Astellas’ Xospata for a certain type of acute myeloid leukaemia (AML) and querying evidence for MSD's Keytruda in head and neck cancer

News

Astellas gets EU approval for AML drug Xospata

The European Commission has approved Astellas’ Xospata (gilteritinib) for patients with relapsed or refractory FLT3-positive acute myeloid leukemia (AML), cementing its lead over a rival dr

News

Daiichi waits on FDA as AML drug quizartinib approved in Jap...

The Japanese regulator has approved Daiichi Sankyo’s quizartinib for certain patients with acute myeloid leukaemia (AML), amid doubts over the outcome of a regulatory review in the US.

News

FDA advisors reject one Daiichi Sankyo cancer drug, back ano...

Daiichi Sankyo had a day of mixed fortunes after advisers to the US regulator voted against approval for its leukaemia drug quizartinib, but recommended pexidartinib for a rare tumour.

FDA grants full approval for Roche/AbbVie's Venclexta in AML...

Gilead to buy immuno-oncology firm Forty Seven for $4.9bn

NICE rejects Astellas' Xospata in AML, queries MSD's Keytrud...

Astellas gets EU approval for AML drug Xospata

Daiichi waits on FDA as AML drug quizartinib approved in Jap...

FDA advisors reject one Daiichi Sankyo cancer drug, back ano...

Neuralink gets okay for its first international trial

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

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