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Author(s):
Jonathan D. Grinstein, PhD, Manfred Scholz, PhD, and Erik Wiklund, PhD, go behind the headlines to address a shifting policy landscape and what it means for the future of chronic disease, diagnostics, and next-generation cell and gene therapies.
Behind the Headlines is a bi-weekly panel discussion examining the latest trends, readouts, and other factors that drive pharmaceutical news and innovation. Each episode features consultants, venture capitalists, scientists, patient advocates, and journalists discussing the prior weeks’ top news while seeking to highlight the more enduring lessons that hide behind the headlines.
In episode 22, Jonathan D. Grinstein, PhD, North American Editor for Inside Precision Medicine; Manfred Scholz, PhD, President of Scholz Consulting Partners; and Erik Wiklund, PhD, CEO of Circio, tackle a shifting policy landscape and what it means for the future of chronic disease, diagnostics, and next-generation cell and gene therapies. They explore what’s rising, what’s receding, and what’s next for precision medicine.
The discussion opens with reflections on a growing realignment in U.S. healthcare priorities—from high-profile acute care innovations toward more long-term strategies for managing chronic illness. The panel agrees that the shift is overdue, citing a large body of data pointing to the long-term burden of untreated and under-managed conditions across the country (1). This shift occurs against a backdrop of geopolitical tensions, including tariffs and widespread staff layoffs affecting the life sciences workforce.
The panel then takes a full-circle look at diagnostics—highlighting both high-opportunity fields and high-need gaps. In addition to established companion diagnostics and biomarker work, attention is turning to emerging tools like dried blood spot testing and acoustic ejection mass spectrometry, which promise faster and more accessible protein biomarker quantification (2).
The regulatory environment for cell and gene therapy continues to evolve. The panel notes the FDA’s recent move to halt Sarepta’s Elevidys distribution and place multiple trials on hold after reported deaths (3), while also citing broader leadership shifts within the agency’s biologics arm. In this climate, in vivo approaches are gaining traction. Examples include Orbital Therapeutics’ non-human primate data for its in vivo CAR-T program in autoimmune disease (4) and ARTBIO’s $132 million Series B raise to advance its radioligand therapy (RLT) platform. While some see RLT as a more promising route for solid tumors, others—like ARTBIO’s Emanuele Ostuni, PhD—suggest that the modalities may work best in tandem. “The alpha particle modality essentially creates a small explosion of antigens in the tumor, which do recruit T cells—a situation ripe with synergistic potential,” he told Inside Precision Medicine (5).
Watch the full episode above for more insights into the evolving biopharma landscape and catch up on previous episodes of Behind the Headlines here.
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