“With that in mind, it is possible we will not reach data cutoff this year, and we look forward to updating you in due course.”

In context

“rately, we're pleased FDA has granted Kite the Regenerative Medicine Advanced Therapy designation, or RMAT, for the evaluation of Yescarta for newly diagnosed high-risk large B-cell lymphoma who have a positive PET scan after two cycles of first-line chemotherapy. Under the RMAT designation, the Yescarta development program for first-line treatment of high-risk large B-cell lymphoma will be able to access the benefits of the FDA's accelerated pathways, including fast-track and breakthrough designations. Our Phase 3 ZUMA-23 study in this setting is ongoing, and we look forward to sharing updates in due course. Moving to our milestones on Slide 23, a brief update on ASCENT-03. As a reminder, this is an event-driven trial, and I can share that we are continuing to accrue events at this time. With that in mind, it is possible we will not reach data cutoff this year, and we look forward to updating you in due course. Other updates this quarter included the readout of PURPOSE 2 data ahead of schedule, the review of our Phase 2 data for Lenacapavir plus our broadly neutralizing antibodies with plans to share the data at an upcoming scientific conference in 2025. The initiation of several key HIV, Trodelvy, and cell therapy trials, including enrollment for ISLEND-1, ISLEND-2, ASCENT-GYN-01, and iMMagine-3. In closing, I'd like to thank the Kite and Gilead Research and Development teams for a stellar quarter of execution. And with that, I'll hand the call over to Andy. Andrew Dickinson : Thank you, Merdad. And good afternoon, everyone. Our third quarter results represent a strong quarter for Gilead. As shown on Slide 25, with our base business up 7% year-over-year to $6.8 billion, driven by growth in each”