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CLAIM #27435 · GILD (GILD) · 2026Q1 earnings call · May 7, 2026 · due Dec 31, 2026

Additionally, we expect FDA regulatory decisions for Biclen in August and anitocel in December, as well as Phase 3 updates for ILLAND-1 and -2 in the first half of this year, and for EVOQUE-3, ASCENT GYN, and IDEAL in the second half.

Dietmar Berger · Chief Medical Officer

PENDING
graded after results covering Dec 31, 2026 are reported

How to check this claim

Look at: Occurrence of stated regulatory/clinical milestones: FDA decision on Biclen, FDA decision on anitocel, Phase 3 data updates for ILLAND-1/-2, EVOQUE-3, ASCENT GYN, and IDEAL

It came true if: FDA action on Biclen disclosed by end of August 2026; FDA action on anitocel disclosed by end of December 2026; ILLAND-1 and -2 Phase 3 updates disclosed by June 30, 2026; EVOQUE-3, ASCENT GYN, and IDEAL Phase 3 updates disclosed by December 31, 2026

Where: Company press releases, FDA announcements, and Gilead quarterly earnings calls/presentations in 2026

In context

r we plan to share updates from our broader inflammation portfolio, including the Phase 3 IDEAL study evaluating Libdelzi in PBC patients with incomplete response to UDCA, the Phase 2 SWIFT study evaluating GS-1427 or envistigraf, our investigational oral alpha4beta7 inhibitor for inflammatory bowel diseases, and the Phase 2a COSMIC study evaluating usertib, our investigational IRAK4 kinase inhibitor, in cutaneous lupus erythematosus. Finally, reviewing our 2026 pipeline milestones on slide 20, we remain on track across all our key deliverables. We expect an FDA regulatory decision for bulevirtide as a treatment for chronic HDV infection later this quarter. Bulevirtide has been approved as Hepcludex in the EU since 2020, and we look forward to making this available to patients in the U.S. Additionally, we expect FDA regulatory decisions for Biclen in August and anitocel in December, as well as Phase 3 updates for ILLAND-1 and -2 in the first half of this year, and for EVOQUE-3, ASCENT GYN, and IDEAL in the second half. With that, I would like to thank our research and development teams and our partners, whose continued strong clinical execution are driving the progress we have seen across our pipeline. Now I will turn over the call to Andy. Andrew Dickinson: Thank you, Dietmar. Good afternoon, everyone. As you have heard, Gilead Sciences, Inc. delivered strong first quarter results with continued commercial outperformance and disciplined operating execution. As shown on slide 22, our base business grew 8% year-over-year, to $6.8 billion, driven by continued growth in sales for HIV products, Trodelvy, and Libdelzi, partially offset by lower sales of HCV and cell therapy products. Sequentially, sales were down 12%, reflecting typical seasonal inventory dynamics in line with our expectations. Total product

Verify independently

SEC filings for GILD · Claim quote is verbatim from the 2026Q1 earnings call.