The new approval expands the drug's indication to include treatment in adult patients with unresectable locally advanced or metastatic triple-negative breast cancer.
Gilead’s Trodelvy (sacituzumab govitecan-hziy), received full FDA approval and an expanded indication for patients with advanced or metastatic triple-negative breast cancer (TNBC).
The FDA granted accelerated approval to Trodelvy a year ago, but the new approval expands the drug's indication to include treatment of adult patients with unresectable locally advanced or metastatic TNBC who have received two or more prior systemic therapies, at least one of them for metastatic disease.
Related: MacroGenics’ treatment for HER2-positive breast cancer to be available in March
The commercial list price or Trodelvy is around $2,100 per vial, a spokesperson told FormularyWatch®. The cost of therapy is dependent on patient weight and duration of treatment, the spokesperson said.
Trodelvy is directed to the Trop-2 receptor, a protein frequently expressed in multiple types of epithelial tumors, including TNBC, where high expression is associated with poor survival and relapse, Gilead said in a press release. Prior Trodelvy’s approval, patients with previously treated metastatic TNBC had few treatment options, according to Gilead.
“Women with triple-negative breast cancer have historically had very few effective treatment options and faced a poor prognosis,” said Aditya Bardia, MD, MPH, director of Breast Cancer Research Program, Mass General Cancer Center; assistant professor of medicine at Harvard Medical School, and global principal investigator of the ASCENT study.“[FDA’s] approval reflects the statistically significant survival benefit seen in the landmark ASCENT study and positions sacituzumab govitecan-hziy as a potential standard of care for pre-treated TNBC.”
In the Phase 3 ASCENT study, Trodelvy demonstrated a statistically significant and clinically meaningful 57% reduction in the risk of disease worsening or death (progression-free survival (PFS), extending median PFS to 4.8 months from 1.7 months with chemotherapy.
Trodelvy also extended median overall survival (OS) to 11.8 months versus 6.9 months, a 49% reduction in the risk of death.
Trodelvy carries a Boxed Warning for severe or life-threatening neutropenia and severe diarrhea.
Read more: FDA okays novel breast, colorectal cancer treatments
AstraZeneca, Daiichi Sankyo Submit New BLA for Datopotamab in Lung Cancer
November 12th 2024After feedback from the FDA, the companies have voluntarily withdrawn the previous biologics licensing application for datopotamab deruxtecan for patients with advanced or metastatic nonsquamous non-small cell lung cancer.
Read More
Skyrizi Overtakes Humira in U.S. Sales Numbers
November 8th 2024For the first time, Skyrizi has replaced Humira as AbbVie’s sales driver, largely due to companies encouraging “product hopping” to avoid competition, creating concerns for the sustainability of the burgeoning adalimumab biosimilar market.
Read More