Immunomedics’ ASCENT Confirms Trodelvy’s Efficacy In Triple-Negative Breast Cancer

After accelerated approval in the US in April based on Phase II response rates, the company will seek full approval later this year based on a tripling of progression-free survival in a Phase III trial.

Healthcare success and patients to succeed in medical care or successful doctor concept as a stethoscope solving a maze to hit the target and succeed as a 3D illustration.
Trodelvy could find its way to more TNBC patients based on Phase III data • Source: Shutterstock

Immunomedics, Inc. reported top-line results from the Phase III ASCENT clinical trial on 6 July for Trodelvy in which progression-free survival (PFS) was three times as long for patients with previously treated metastatic triple-negative breast cancer (TNBC) who were treated with the antibody-drug conjugate (ADC) targeting Trop-2 compared with patients who received chemotherapy. More detailed results could improve uptake and reimbursement for the recently launched product.

Trodelvy (sacituzumab govitecan-hziy) received accelerated US Food and Drug Administration approval in April for the treatment of metastatic TNBC patients who have received at least two prior lines of therapy based on the objective response rate (ORR) in a Phase II study

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