Where the field is going right now is to maximize efficacy as well as safety. So in order to maximize the efficacy, the field is testing doublet or triplet combinations in the upfront settings as well as the relapse refractory setting. In terms of maximization of the safety, the trials are now looking into the treatment breaks. And one of the approaches that we have taken in the specific trial of Pirtobrutinib and Acalabrutinib was to take an artificial break after about one year of therapy...
Where the field is going right now is to maximize efficacy as well as safety. So in order to maximize the efficacy, the field is testing doublet or triplet combinations in the upfront settings as well as the relapse refractory setting. In terms of maximization of the safety, the trials are now looking into the treatment breaks. And one of the approaches that we have taken in the specific trial of Pirtobrutinib and Acalabrutinib was to take an artificial break after about one year of therapy. So I think the more maturing data from these trials would be helpful for us to determine the future directions. In the U.S. setting right now, the treatments are largely divided into two methods. One is to use a continuous treatment with one of the BTK inhibitors, a more selective one. The other approach is combination over a fixed duration or MRD-guided duration of the time. And there are several combinations in that category.
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