Benzinga | Nov 29, 2021 08:31AM EST

Gilead Says Co's Bold Ambition Of Transforming Triple-Negative Breast Cancer Treatment To Be Highlighted With New Data At SABCS

Gilead Sciences, Inc. (NASDAQ:GILD) will present additional data from the Phase 3 ASCENT study of Trodelvy(r) (sacituzumab govitecan-hziy) during the upcoming San Antonio Breast Cancer Symposium (SABCS) being held from December 7-10. These data reinforce the benefits of Trodelvy and the importance of Gilead's transformative science in cancers with high unmet need. In the United States, Trodelvy is indicated for the treatment of adult patients with unresectable locally advanced or metastatic triple-negative breast cancer (TNBC) who have received two or more prior systemic therapies, at least one of them for metastatic disease.

"Our data at SABCS add to the growing body of evidence supporting the use of Trodelvy for people with metastatic TNBC," said Merdad Parsey, MD, PhD, Chief Medical Officer, Gilead Sciences. "We continue to advance the treatment of TNBC and are actively exploring the potential of Trodelvy across the breast cancer landscape."

Highlights at the meeting include an ASCENT analysis examining outcomes for Black patients with metastatic TNBC who were treated with Trodelvy compared to those receiving physician's choice of chemotherapy. Additional ASCENT analyses will explore health-related quality of life (HRQoL) measures by clinical response and post-progression treatment and survival of patients who experienced continued disease progression.

Accepted abstracts are as follows:

* Assessment of Sacituzumab Govitecan in Black Patients from the Phase 3 ASCENT Study in Metastatic Triple-Negative Breast Cancer (Poster #P5-16-07)

* Post-Progression Therapy Outcomes in Patients from the Phase 3 ASCENT Study of Sacituzumab Govitecan in Metastatic Triple-Negative Breast Cancer (Poster # P5-16-15)

* Assessment of Health-Related Quality of Life by Clinical Response from the Phase 3 ASCENT Study in Metastatic Triple-Negative Breast Cancer (Poster #P5-16-01)

The presentations will be made available in-person and on-demand as part of Poster Session 5 beginning Friday, December 10 at 7:00 a.m. CT.

For more information, including a complete list of abstract titles at the meeting, please visit: https://www.sabcs.org/Program/Schedule-at-a-Glance.

The Trodelvy U.S. Prescribing Information has a BOXED WARNING for severe or life-threatening neutropenia and severe diarrhea; see below for Important Safety Information.