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BioWorld - Wednesday, April 1, 2026
Breaking News: Trump administration impacts continue to roil the life sciences sectorBreaking News: Trump administration impacts continue to roil the life sciences sector
Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory front

Canada raises wall to protect its drug supply from U.S.

Nov. 30, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Pandemic not the time for trade restrictions; Longer-term vaccine follow-up crucial; Labeling update advised for chloroquines; FDA stands up new DDT path; FDA drafts DDI guidance; MHRA continues Brexit updates; FDA debars three.
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Regulatory actions for Nov. 30, 2020

Nov. 30, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Antengene, Aprea, Ars, Astellas, Astrazeneca, Cassava, Chiesi, Recordati, Exelixis, Fibrogen, Innovation, Iterum, Kadmon, Mirum, Otonomy, Prevail, Protalix, Regeneron, Rhythm, Sedana, Takeda, Vertex, Y-mabs, Zymeworks.
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Brain

FDA grants approval for Y-mabs neuroblastoma therapy Danyelza

Nov. 30, 2020
By Michael Fitzhugh
Just ahead of the U.S. celebration of Thanksgiving, the FDA granted an accelerated approval for Danyelza (naxitamab), a new therapy for certain adults and children with relapsed or refractory high-risk neuroblastoma. The antibody, which Y-mabs Therapeutics Inc. initially sublicensed via a deal with Mabvax Therapeutics Inc. in 2018, is approved for use in combination with granulocyte macrophage colony-stimulating factor. The regulator had assigned the BLA a Nov. 30 PDUFA date.<
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Regulatory front

HHS seeks feedback on future of pandemic policies

Nov. 25, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: The other shoe drops for former Insys CEO; NICE gives nod to new myeloma regimen; MHRA prepares for January; FDA guidances finalized.
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Regulatory actions for Nov. 25, 2020

Nov. 25, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Altimmune, Basilea, Bio-Thera, Janssen, Liquidia, Pfizer, Polaryx, Reata, Revance, Rhovac, Sirtex.
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Architectural pillars

Let the challenges begin

Nov. 24, 2020
By Mari Serebrov
The Pharmaceutical Research and Manufacturers Association (PhRMA) filed suit Nov. 23 in U.S. district court challenging the Trump administration’s final rule allowing the import of prescription drugs from Canada.
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FDA approved metal stamp

Oxlumo for preventing kidney disease is Alnylam’s third FDA approval

Nov. 24, 2020
By Lee Landenberger
Four days after receiving European approval, the FDA has followed suit for Alnylam Pharmaceuticals Inc.’s Oxlumo (lumasiran), the first treatment for primary hyperoxaluria type 1, an ultra-rare genetic disorder that contributes to kidney stones and deposits.
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Chinese flag, pills

China further bolsters cell therapy development with dual-track regulatory framework

Nov. 24, 2020
By Elise Mak
SHENZHEN – To accelerate the development of cell therapies, China’s NMPA has introduced a dual-track regulatory pathway that allows companies to seek an IND with data from investigator-initiated trials.
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Regulatory actions for Nov. 24, 2020

Nov. 24, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Alnylam, Appili, BMS, F-star, Mustang, Obseva, Polypid, Viatris.
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Regulatory front

FDA’s ‘misguided’ drug program to be withdrawn

Nov. 24, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Unapproved Drugs Initiative.
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