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EMA Recommends Granting a Marketing Authorisation for Sacituzumab Govitecan

It is indicated for the treatment of adult patients with unresectable or metastatic TNBC who have received two or more prior systemic therapies
25 Oct 2021
Anticancer agents & Biologic therapy;  Breast cancer

On 14 October 2021, the European Medicines Agency’s (EMA’s) Committee for Medicinal Products for Human Use (CHMP) adopted a positive opinion, recommending the granting of a marketing authorisation for the first-in-class medicinal product sacituzumab govitecan (Trodelvy), intended for the treatment of unresectable or metastatic triple negative breast cancer (TNBC).

Trodelvy was reviewed under EMA’s accelerated assessment programme.

The applicant for this medicinal product is Gilead Sciences Ireland UC.

Trodelvy will be available as a 200 mg powder for concentrate for solution for infusion. The active substance of Trodelvy is sacituzumab govitecan, an antineoplastic agent (ATC code: L01FX17). It combines a humanised monoclonal antibody, which binds to Trop-2-expressing cancer cells, and a linked cytotoxic moiety SN-38 (govitecan), which inhibits topoisomerase I, preventing DNA repair and leading to apoptosis and cell death.

The benefits of Trodelvy are its improved progression-free survival (PFS) and overall survival (OS) in patients with unresectable locally advanced or metastatic TNBC which had relapsed after at least two prior chemotherapies, when compared with treatment of physician’s choice in a phase III, multicentre, open-label, randomised study.

The CHMP based its recommendation on data from a phase III, multicentre, open-label, randomised clinical study that study investigated the safety and efficacy of Trodelvy in 529 patients with unresectable locally advanced or metastatic TNBC. All patients enrolled had relapsed after at least two prior chemotherapies for breast cancer. Participants were randomised (1:1) to receive sacituzumab govitecan 10 mg/kg as an intravenous infusion on days 1 and 8 of a 21-day cycle or treatment of physician’s choice (eribulin, vinorelbine, gemcitabine, or capecitabine).

The medicine prolonged the OS by approximately 5 months (11.8 months for sacituzumab govitecan compared to 6.9 months for treatment of physician’s choice) and the PFS by about 3 months (4.8 months for sacituzumab govitecan compared to 1.7 months for treatment of physician’s choice).

The most common side effects are diarrhoea, nausea, neutropenia, fatigue, alopecia, anaemia, vomiting, constipation, decreased appetite, cough, and abdominal pain.

The full indication is:

Trodelvy as monotherapy is indicated for the treatment of adult patients with unresectable or metastatic TNBC who have received two or more prior systemic therapies, including at least one of them for advanced disease.

Trodelvy must only be prescribed to patients by healthcare professionals experienced in the use of cancer.

Detailed recommendations for the use of this product will be described in the summary of product characteristics, which will be published in the European public assessment report and made available in all official European Union languages after the marketing authorisation has been granted by the European Commission.

Once a marketing authorisation has been granted, decisions about price and reimbursement will take place at the level of each Member State, taking into account the potential role/use of this medicine in the context of the national health system of that country.

Summaries of positive opinion are published without prejudice to the Commission decision, which will normally be issued 67 days from adoption of the opinion.

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