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BioWorld - Wednesday, July 1, 2026
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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Two to go: J&J the latest pharma to reach MFN drug pricing deal

Jan. 9, 2026
By Jennifer Boggs
No Comments
And another firm has reached a most-favored nation (MFN) pricing deal with the White House. Johnson & Johnson announced Jan. 8 a voluntary agreement with the Trump administration aimed at improving access and lowering prices for medications in the U.S., in exchange for exempting the pharma firm’s products from tariffs.
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FDA rejects Vanda’s Hetlioz for jet lag disorder

Jan. 8, 2026
No Comments
Debate over Vanda Pharmaceuticals Inc.’s Hetlioz (tasimelteon) for use in jet lag disorder looks to continue after the U.S. FDA rejected the latest supplemental NDA submission, with the agency’s Center for Drug Evaluation and Research concluding the application cannot be approved in its current form.
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Hutchmed plans China NDA filing of sovleplenib in rare anemia

Jan. 8, 2026
By Marian (YoonJee) Chu
No Comments
Hutchmed Ltd. plans to file a second NDA in China for sovleplenib, a novel spleen tyrosine kinase inhibitor, based on positive phase II/III findings in warm antibody autoimmune hemolytic anemia.
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Cells and DNA helix

South Korea enacts world’s first regulation on synthetic biology

Jan. 7, 2026
By Marian (YoonJee) Chu
No Comments
South Korea will implement a new regulation on synthetic biology in April 2026, aiming to foster innovations across both biotechnology and biomanufacturing.
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U.S. vaccine illustration

Industry considering options amid US vaccine upheaval

Jan. 7, 2026
By Mari Serebrov
No Comments
The chaos Health and Human Services Secretary Robert Kennedy has injected into the U.S. vaccine market could have long-term consequences as vaccine makers reevaluate business decisions and pipelines.
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Appeals court says no to cap on indirect costs in NIH grants

Jan. 6, 2026
By Mari Serebrov
No Comments
Unless the U.S. Supreme Court steps in to reverse the decision, the NIH’s attempt to cap indirect costs at 15% in all its grants is dead. The U.S. Court of Appeals for the First Circuit upheld a permanent injunction Jan. 5 that was issued by a lower court, vacating an NIH supplemental guidance imposing the across-the-board cap both retroactively and prospectively.
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Gold won currency symbol on black background

South Korea approves record budgets for health agencies in 2026

Jan. 6, 2026
By Marian (YoonJee) Chu
No Comments
South Korea’s National Assembly approved the largest budgets for its health ministries in 2026, including the Ministry of Health and Welfare, Ministry of Food and Drug Safety and Korea Disease Control and Prevention Agency.
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Yellow umbrella in a storm

Stormy year in biopharma forecast

Jan. 6, 2026
By Mari Serebrov
No Comments
It doesn’t take a meteorologist to predict another stormy year for the biopharma sector, not just in the U.S., but also in Europe. Lurking within those storms, though, could be a few silver linings.
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US vaccine schedule slashed to international standards

Jan. 5, 2026
By Mari Serebrov
No Comments
With the stroke of a pen and no input from the CDC’s Advisory Committee for Immunization Practices, acting CDC Director Jim O’Neill cut the number of vaccines the agency routinely recommends for children to 11 on Jan. 5, down from 17 in 2024.
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Scinopharm wins US FDA approval of multiple sclerosis drug

Jan. 5, 2026
By Marian (YoonJee) Chu
No Comments
Scinopharm Taiwan Ltd. received U.S. FDA approval for its generic version of glatiramer acetate injection, a treatment for multiple sclerosis.
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