Lunsumio

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After FDA no, Regeneron gets yes from EU on odronextamab

Regeneron's CD20xCD3 bispecific antibody for non-Hodgin lymphoma (NHL) has been approved in Europe, five months after it was turned down by the FDA in the US.

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FDA starts swift review of Regeneron’s CD20 bispecific

The FDA has started a priority review of Regeneron’s CD20xCD3 bispecific antibody odronextamab, seeking a broader label than other drugs in the class.

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CD20 market heats up as FDA OKs AbbVie, Genmab bispecific

AbbVie and partner Genmab have FDA approval for the lead drug in their $3.9 billion cancer

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Roche claims US approval for lymphoma bispecific Lunsumio

The FDA has given a green light to Roche's CD20xCD3 bispecific antibody Lunsumio as a treatment for relapsed or refractory follicular lymphoma, following the lead of the European Commission

News

ASH: CD20 bispecific antibodies take centre stage in lymphom...

As Roche heads towards an FDA verdict on its CD20xCD3 bispecific Lunsumio for lymphoma before the end of this year, rivals from Regeneron and AbbVie are starting to nip at its heels, with n

News

FDA to decide on Roche's lymphoma drug Lunsumio before year-...

The FDA has granted a priority review to Roche's T-cell engager Lunsumio as a treatment for follicular lymphoma (FL), setting up a decision on the drug by 29 December.

After FDA no, Regeneron gets yes from EU on odronextamab

FDA starts swift review of Regeneron’s CD20 bispecific

CD20 market heats up as FDA OKs AbbVie, Genmab bispecific

Roche claims US approval for lymphoma bispecific Lunsumio

ASH: CD20 bispecific antibodies take centre stage in lymphom...

FDA to decide on Roche's lymphoma drug Lunsumio before year-...

NIH algorithm matches patients to clinical trials

Decoding physician prescribing behaviour: A data-driven jour...

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