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Amgen has secured full approval from the U.S. Food and Drug Administration for its new therapy designed for adults with extensive stage small cell lung cancer who have progressed after platinum-based chemotherapy.
This approval marks a significant milestone for the biopharmaceutical company, enhancing its portfolio in the oncology sector and providing a vital treatment option for patients facing this aggressive form of cancer.
The advancement deepens Amgen’s strategic foothold in oncology just as the company prepares for a critical financial update. Investor attention is expected to center on implications for revenue streams during Amgen’s upcoming Q3 2025 financial results announcement, a key event for evaluating the broader impact of new therapeutic approvals on the company’s long-term outlook.