Answer extracted from the Morning Brew Daily podcast — listen to the full episode below.
RasenQ, developed by Revolution Medicines, is the first drug to successfully target the KRAS protein—a driver of nearly all pancreatic cancers that was previously considered undruggable due to its smooth surface. In late-stage trials, patients on RasenQ lived over 13 months on average compared to 6.7 months for those receiving standard chemotherapy. The FDA approved it this week, marking a fundamental shift in how pancreatic cancer can be treated.
For decades, the KRAS protein remained a frustrating puzzle for oncologists. Its shape made it nearly impossible to bind pharmaceutical molecules to it—hence the label "undruggable." Pancreatic cancer, which affects over 60,000 people annually in the United States, has long carried one of the poorest survival rates among major cancers, with KRAS mutations present in approximately 90% of all pancreatic cancer cases.
Revolution Medicines' breakthrough lies in a novel molecular approach that finally cracked this obstacle. As detailed in the episode, the drug's ability to bind to KRAS represents years of targeted research. This single approval opens the door to an entirely new class of cancer therapeutics that had been written off as impossible.
The clinical evidence is striking. In the phase 2b study that led to FDA approval, the 13-month average survival extension doubled the historical baseline for pancreatic cancer patients. This is not a marginal improvement—it signals a potential paradigm shift in how the disease is managed. The sticker price, at nearly $40,000 per month or approximately $478,000 annually, reflects both the complexity of the drug's development and the market's assessment of its clinical value.
Financial markets have already reacted decisively. Revolution Medicines shares are up nearly 180% in 2025, and analysts project RasenQ will generate more than $9 billion in annual sales by 2032. For oncology investors and patients alike, this approval represents proof that previously untargatable proteins can be addressed with enough ingenuity and investment, potentially unlocking treatments for other historically difficult-to-drug cancers.
KRAS is a protein that, when mutated, drives the growth of multiple cancer types, most notably pancreatic cancer. It was considered "undruggable" because its smooth molecular surface lacked the binding pockets that conventional drug molecules could attach to, making it extremely difficult to inhibit pharmacologically until RasenQ's novel mechanism overcame this barrier.
For more context on how this breakthrough fits into the broader biotech and pharma landscape, listen to Morning Brew Daily for the full episode discussion, which also explores the broader implications of targeted cancer therapies and the timelines for patient access to this new treatment.
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