“In addition to the ongoing launch of Libdelzi, and the potential launch of lenacapavir for PrEP in 2025, we are also looking forward to the potential launch of anetocel in multiple myeloma and Trodelvy in first-line metastatic triple-negative breast cancer in 2026.”

In context

“oadly, we continue to raise awareness of the strength of our data, the advantages of a one-time treatment, and the potential benefits of earlier CAR T. Notwithstanding the ongoing competitive headwinds, that we continue to expect to extend through 2025, we remain very excited about the overall opportunity and future for cell therapy. The potential launch of anetocel in multiple myeloma in 2026, and exciting early-stage data in our next-generation products across lymphoma, and solid tumors at ASCO. Before I hand over to Dietmar, I'd like to thank the commercialization team for delivering a great start to the year. We remain focused on expanding the reach of our current portfolio but are also very excited about the rich pipeline of near-term launches over the next twelve to eighteen months. In addition to the ongoing launch of Libdelzi, and the potential launch of lenacapavir for PrEP in 2025, we are also looking forward to the potential launch of anetocel in multiple myeloma and Trodelvy in first-line metastatic triple-negative breast cancer in 2026. And with that, I'll hand the call over to Dietmar. Dietmar Berger: Thank you, Johanna, and good afternoon, everyone. We have made a lot of progress in the first quarter, with some exciting lenacapavir updates at CROI, and our first pivotal Phase III top-line readout for Trodelvy in breast cancer since 2022. The quality of these readouts highlights the breadth and depth of clinical expertise across Gilead Sciences, Inc., with the potential to support growth in our target therapeutic areas with new commercial launches in the years ahead. Starting with HIV on slide 15, we shared 20 abstracts at CROI, including data that showcase lenacapavir's potential even beyond the remarkable results we saw in PURPOSE 1 and PURPOSE 2 last year. For example, we shared our phase one data that showed once-ye”