Published Date: 27 May 2023
The decision by the regulator's advisory panel to postpone an accelerated approval caused worries about the prospects of Intercept's drug to treat a specific form of fatty liver disease, which caused shares of the company to drop by about 16% on Monday.
Read Full NewsThe recommendation follows phase 3 data showing longer progression-free survival when patients switched to camizestrant plus a CDK4/6 inhibitor.
The antibody drug conjugate was approved by the FDA for certain patients with triple-negative breast cancer.
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