The European Medicines Agency's Committee For Medicinal Products For Human Use Has Adopted A Positive Opinion Recommending Gilead Sciences' Trodelvy (Sacituzumab Govitecan) As Monotherapy In Pre-Treated HR+/HER2- Metastatic Breast Cancer
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The European Medicines Agency's Committee for Medicinal Products for Human Use has recommended Gilead Sciences' Trodelvy for pre-treated HR+/HER2- metastatic breast cancer.
June 23, 2023 | 12:14 pm
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Gilead Sciences' Trodelvy receives positive recommendation from EMA committee for pre-treated HR+/HER2- metastatic breast cancer.
The positive recommendation from the European Medicines Agency's Committee for Medicinal Products for Human Use is a significant step towards the approval of Trodelvy in Europe. This could lead to increased sales and revenue for Gilead Sciences, positively impacting the stock price in the short term.
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