April 23, 2025
| This week’s commercialization news and insights for biopharma leaders
A spokesperson confirmed the Danish drugmaker has asked U.S. regulators to clear an oral version of its weight loss drug Wegovy two years after reporting initial Phase 3 results.
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A late-stage study found Cobenfy wasn’t better than a placebo as an add-on to atypical antipsychotics. Some analysts view the failure as a “significant hit” to the drug’s commercial outlook.
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The big pharma joined several of its peers in committing to invest billions of dollars in new and expanded manufacturing facilities in the U.S.
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Progress in gene editing, messenger RNA and cell therapies is promising new kinds of medicines in the future. Explore the current biotech landscape and what’s next in
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The partners overcame an earlier rejection to win a seventh use for Dupixent, though some analysts are skeptical of its sales potential compared to other emerging medicines for the condition.
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The law in particular will affect CVS and UnitedHealth, both of which operate physical pharmacies in the state along with specialty and mail-order pharmacy businesses.
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The committee endorsed lowering the age at which some people can receive RSV vaccines, but stopped short of recommending booster shots.
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News roundup
U.K. regulators cleared a multiple myeloma drug GSK withdrew from market three years ago. Elsewhere, an investment firm pressed Elevation Oncology to liquidate and the FDA relaxed risk monitoring requirements for Camzyos.
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