This is an important question as well because until now, so in current days, the epcoritamab is approved as a monotherapy for the third plus line treatment. The epcoritamab plus R-CHOP is tested in the first line and if this study is successful, then definitely probably will be not so much space for the patients who fail combination of the bispecific antibody plus R-CHOP in the first line...
This is an important question as well because until now, so in current days, the epcoritamab is approved as a monotherapy for the third plus line treatment. The epcoritamab plus R-CHOP is tested in the first line and if this study is successful, then definitely probably will be not so much space for the patients who fail combination of the bispecific antibody plus R-CHOP in the first line. But in the current situation we know that we need to bring the bispecific antibodies to the second line. This is our study, is the first step, but we know about the STARGLO study, which unfortunately, it was not approved in the US because of some questions regarding the Caucasian population. But definitely, we need to improve the response of those patients in the second line as well. So it means the epco, the other bispecific antibodies, are very good candidates.
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