“We are continuing to look at all global markets. And I would point out, as Dean points out, we're looking at the '25, '26 RSV season, so next year. And then beyond that, we will go globally thereafter.”

In context

“ducation is required to access the private market? Thank you. Dean Li: Yes. So let me just level set in relationship to clesrovimab, and the RSV antibody. So we have the data, and that data will be presented at some time in the second half of this year as the different plenary sessions of different conferences occur. In relationship to filing, our plan is to file such that it would be available, not for this season, but for the next season within the United States. And so that's the sort of next wave in relationship. So I want to make sure that there's no concept that this is coming out this RSV season. We're targeting next RSV season in relationship to when we're seeking approval and licensure. Rob Davis: Yes. And maybe just on the broader question, could this be an opportunity in China. We are continuing to look at all global markets. And I would point out, as Dean points out, we're looking at the '25, '26 RSV season, so next year. And then beyond that, we will go globally thereafter. And China is a market we are looking at. Peter Dannenbaum: Great. Thank you, Luisa. Next question, please, Brad. Operator: The next question comes from Dana Graybosch of Leerink. Your line is open. Dana Graybosch: Hi, thank you for the question. I want to ask about the recent ODAC that was on periadjuvant [ph] development in lung cancer. I wonder, let's assume FDA takes a hard line on requiring the contribution of the neoadjuvant and adjuvant phases. And you look forward to the current KEYTRUDA development program. Do you see any risk to that hard line to any of your label extension plans? And how are you going back to looking at your development, especially of novel combos in the early stage given that discussion. Thank you. Rob Davis: Thank you very much. So just to provide some context”