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Pharmaceutical Executive Daily: September 18,2025

In today’s Pharmaceutical Executive Daily, we explore how AI is disrupting higher education and career pathways, AllRock Bio’s $50 million Series A funding to advance its lead molecule, and FDA warning letters issued to Novo Nordisk, Eli Lilly, and Hims over misleading drug advertising.

Welcome to Pharmaceutical Executive Daily, your quick briefing on the top news shaping the pharmaceutical and life sciences industry.

In today’s Pharmaceutical Executive Daily, we explore how AI is disrupting higher education and career pathways, AllRock Bio’s $50 million Series A funding to advance its lead molecule, and FDA warning letters issued to Novo Nordisk, Eli Lilly, and Hims over misleading drug advertising.

A new analysis highlights how artificial intelligence is reshaping higher education and workforce planning—even for top students. The piece argues that AI’s rapid adoption across industries is forcing even valedictorians to rethink their career trajectories, as skills once considered a long-term advantage risk becoming obsolete. For life sciences employers, the shift underscores the importance of developing flexible career playbooks and investing in continuous upskilling to ensure the next generation of professionals remains competitive in an AI-driven economy.

In biotech funding news, AllRock Bio has secured $50 million in Series A financing to advance its lead molecule, ROC-101. The company is focused on innovative approaches to treating cancer, and the funding round is expected to accelerate development and expand research capabilities. Investors see the move as a vote of confidence in AllRock’s science and its leadership team, positioning the biotech as a company to watch within the increasingly competitive oncology space. Early-stage funding momentum like this continues to signal strong interest in targeted therapeutics, even amid broader biotech market volatility.

And finally, the FDA has issued warning letters to Novo Nordisk, Eli Lilly, and telehealth company Hims, citing misleading advertising practices related to GLP-1 therapies. Regulators said certain promotional materials overstated benefits or downplayed risks, raising concerns about patient safety and compliance. The action serves as a reminder that even as demand for obesity and diabetes treatments surges, manufacturers and their partners must adhere strictly to FDA advertising standards. The warning letters could also spur closer scrutiny of digital marketing strategies across the sector.

Thanks for listening to Pharmaceutical Executive Daily. For more updates and in-depth analysis, visit PharmExec.com.

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