CLAIM #27407 · GILD (GILD) · 2026Q1 earnings call · May 7, 2026 · due Dec 31, 2026
“We are also expecting Phase 3 updates from the EVOQUE-3 trial in first-line metastatic non-small cell lung cancer and the ASCENT GYN trial in second line-plus metastatic endometrial cancer in the second half of this year.”
Daniel O'Day · CEO
How to check this claim
Look at: Public disclosure of Phase 3 trial updates (data readout or results announcement) for EVOQUE-3 (first-line metastatic NSCLC) and ASCENT GYN (second-line-plus metastatic endometrial cancer)
It came true if: At least one company-disclosed update (press release, conference presentation, or publication) on trial results/status for each of EVOQUE-3 and ASCENT GYN occurring between 2026-07-01 and 2026-12-31
Where: Company press releases, investor presentations, or medical conference disclosures (e.g., ASCO/ESMO abstracts) referenced on Gilead's investor relations site
In context
“y oral for virally suppressed people with HIV. We shared encouraging Phase 1 data at CROI in February for a long-acting integrase inhibitor GS-3242. Later this year, we plan to share additional data that support the combination of GS-3242 with lenacapavir as a potential twice-yearly injectable treatment regimen. The time frame for potential launch is between 2031 and 2033. In oncology, first quarter Trodelvy sales were up 37% year-over-year, reflecting growing demand for Trodelvy. We anticipate regulatory decisions on extending into first-line metastatic triple-negative breast cancer in the second half of this year. Ahead of these decisions, Trodelvy has already received NCCN category 1 recommendations across the first line and is the leading ABC and second-line metastatic TNBC treatment. We are also expecting Phase 3 updates from the EVOQUE-3 trial in first-line metastatic non-small cell lung cancer and the ASCENT GYN trial in second line-plus metastatic endometrial cancer in the second half of this year. The pending acquisition of Tubulus is another significant milestone in building Gilead Sciences, Inc.'s oncology franchise. The company brings a clinical-stage candidate, TUV-40, which we believe has the potential to be a leading ADC in ovarian cancer and a next-generation ADC platform with a promising early pipeline. At the upcoming ASCO meeting, we look forward to additional Phase 1 data on TUV-40 in platinum-resistant ovarian cancer. Additionally, we are expecting a regulatory decision on anitocel, our potential best-in-disease BCMA CAR T, in December. Our acquisition of Arcellx, which closed on April 28, reflects our conviction in the potential of anitocel as a differentiated option for patients with multiple myeloma. Given the significant opportunity in fourth line as well as earlier”
Verify independently
SEC filings for GILD ↗ · Claim quote is verbatim from the 2026Q1 earnings call.