Ongoing right now, as far as practice-changing studies, we will have the MANGROVE study, which is Zanubrutinib and Rituximab versus BR, that we’ll hopefully be reading out very shortly. In this clinical protocol, obviously, it’ll be evaluating a truly chemo-free regimen versus BR. Just some context, obviously, we have the British study, ENRICH, that looked at ibrutinib and Rituximab versus BR or R-CHOP, which showed equivalency to BR, so it’ll be very curious to see how this study reads out with the caveat that MANGROVE did not allow any Rituximab maintenance for the BR arm, so that may play some part in the progression-free survival...
Ongoing right now, as far as practice-changing studies, we will have the MANGROVE study, which is Zanubrutinib and Rituximab versus BR, that we’ll hopefully be reading out very shortly. In this clinical protocol, obviously, it’ll be evaluating a truly chemo-free regimen versus BR. Just some context, obviously, we have the British study, ENRICH, that looked at ibrutinib and Rituximab versus BR or R-CHOP, which showed equivalency to BR, so it’ll be very curious to see how this study reads out with the caveat that MANGROVE did not allow any Rituximab maintenance for the BR arm, so that may play some part in the progression-free survival.
In the relapsed/refractory setting, there’s still the ongoing GLOBRYTE study, which is looking at the bispecific antibody Glofitamab versus standard of choice, which is R-squared, lenalidomide-Rituximab, or Bendamustine-Rituximab in patients who progress after BTK inhibitor.
Lastly, there are several ongoing studies looking at some novel CAR T-cell products within the mantle cell lymphoma space, and given unfortunately, we still are not necessarily curing these patients, it’ll be very important to get some more sort of treatment options into this field to help salvage some of these patients.
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