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CLAIM #27217 · GILD (GILD) · 2025Q1 earnings call · Apr 24, 2025 · due Dec 31, 2026

we plan to provide an update on our registrational phase two IMagineOne trial later this year and remain on track to potentially launch anetocel in late-line relapsed refractory multiple myeloma in 2026.

Daniel O'Day · CEO

PENDING
graded after results covering Dec 31, 2026 are reported

How to check this claim

Look at: Company-disclosed update on IMagineOne phase two trial (anetocel) and status of anetocel launch for late-line relapsed/refractory multiple myeloma

It came true if: Company issues a trial update on IMagineOne by end of 2025, AND anetocel is launched (commercially available following approval) for late-line relapsed/refractory multiple myeloma by 2026-12-31

Where: Company press releases, quarterly earnings calls, and 10-K/10-Q filings (Gilead/Kite pipeline disclosures)

In context

zumab for first-line PD-L1 positive metastatic triple-negative breast cancer. The results showed a clinically meaningful and statistically significant improvement in progression-free survival over the standard of care. This news represents an important potential benefit for patients. Metastatic TNBC, one of the most aggressive forms of breast cancer, has historically been very difficult to treat. We expect to share the ASCENT-04 data at a medical congress in the near future and to file with global regulatory authorities as quickly as possible. We continue to expect an update later this quarter on the phase three ASCENT-03 study evaluating Trodelvy monotherapy in first-line metastatic triple-negative breast cancer patients who are not candidates for PD-1 inhibitors. Moving to cell therapy, we plan to provide an update on our registrational phase two IMagineOne trial later this year and remain on track to potentially launch anetocel in late-line relapsed refractory multiple myeloma in 2026. We believe that anetocel's clinical profile, combined with Kite's exceptional manufacturing capabilities and industry-leading turnaround time, puts us in a strong position to address the unmet need for patients with multiple myeloma. In inflammation, we are launching Libdelzi in additional markets following approval from the European Commission in February. We look forward to continued momentum as we bring Libdelzi to more people seeking to manage their primary biliary cholangitis with a differentiated option. As we wrap up a strong first quarter performance, we can look forward to continuing positive momentum. We have multiple potential launches ahead, including lenacapavir, anetocel, and now Trodelvy. As a reminder, we have no major LOEs until the end of 2033 and expect to drive top-lin

Verify independently

SEC filings for GILD · Claim quote is verbatim from the 2025Q1 earnings call.