“So we do expect growth in 2024 for Abecma.”

In context

“at these patients are getting. We are very confident and we are very much looking forward to having that dialog and discussion with the regulatory authorities and looking forward to getting this product to the patients as soon as possible. So the second part that you asked about the label updates that the FDA is seeking right now for all CAR-T products around T-Cell malignancies. Once again, we've treated thousands of patients. And from our perspective, as we look into our data, we do not see a positive relationship two (ph) CAR-T cell therapies in terms of Breyanzi and Abecma. So we will continue to have the dialog with the regulators on that as well as we look to the final wording the FDA will decide. With that, let me pass it onto, Adam. Adam Lenkowsky: Thanks, Luisa, for the question. So we do expect growth in 2024 for Abecma. Commentary is a key catalyst for growth this year. And as Samit said, we do look forward to the ODAC to reinforce the benefits of Abecma in a triple exposed patient population. As you can imagine our commercial teams have been launch-ready for some time and we're also seeing continued strong international performance. And we'll launch both Abecma and Breyanzi in a number of new countries this year. We've stated that, we're seeing continued impact from additional BCMA agents. This is a highly competitive market and putting some pressure on Abecma growth. But our teams are squarely focused on opening new accounts, expanding our site footprint, not just internationally, but also in the U.S. And coating the gap on efficacy perception, including solidifying any misconceptions around Abecma's e”