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Putting Americans First: No medicine is more expensive than the one patients can’t access
The most notable differences between the pharmaceutical market in the U.S. and those in other countries are not in the prices. They’re in the […]
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BIO Coffee Chat looks at patient access after three years of the IRA
It has been three years since the Inflation Reduction Act (IRA) was signed into law. “We have definitively seen negative impacts on patient access,
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Riboway Therapeutics: Resilience, RNA, and redefining the undruggable
At this year’s BIO International Convention in Boston, Riboway Therapeutics emerged as the winner of the 2025 BIO Start-Up Stadium seed-stage category. For founder and
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Startup Stadium: Tezcat Biosciences targets common cancer mutation
A Rat sarcoma (RAS) mutation is an oncogene, a gene that causes cancer when mutated. The RAS is the most commonly mutated oncogene in
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Psoriasis awareness: The condition is more than skin deep
Over 8 million people in the U.S., and 125 million worldwide, live with psoriasis—about 2–3% of the population. Far from being a simple cosmetic
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BIO 2025: As M&A slows, biotechs need to show good data
M&A in biotech has slowed from its peak in 2023 but there are still deals to be done, especially for companies who can present
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BIO 2025: How weight loss drugs are disrupting chronic disease
“Initial weight loss is just the first chapter,” said Mia de Graaf, Deputy Executive Health Editor at Business Insider, “but the real challenge and
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BIO 2025: Psychedelics go mainstream – what’s next?
When experts discussed clinical uses of psychedelics two years ago at the 2023 Biotechnology Innovation Organization (BIO) International Convention, there was some interest in
BIO 2025: Psychedelics go mainstream – what’s next? Read More »
Mother inspired to support solutions for her boys’ blindness
For most of her life, the only things coming out of left field for Kristin Smedley were fly balls, but with the birth of
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BIO experts discuss challenges and offer opportunities for developing redosable gene therapies
As drug makers work to develop safe, effective gene therapies, their progress can be slowed when they challenge the limits of established regulatory guidance