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BioWorld - Wednesday, January 14, 2026
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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New York Stock Exchange building

U.S. lawmakers look to close trading loopholes

Sep. 17, 2020
By Mari Serebrov
Spurred by reports of biopharma executives exercising stock options in conjunction with announcements about COVID-19 vaccine developments and government contracts, U.S. lawmakers want to close the loopholes that make such actions legal.
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Regulatory front

USPTO launches pilot for COVID-19 drugs, devices

Sep. 17, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: Bladder cancer therapies evaluated.
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Regulatory actions for Sept. 17, 2020

Sep. 17, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Allovir, Celltrion, Chemocentryx, Chi-Med, Roche, Sorrento, Zynerba.
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Biopharma companies draw ire for stepping into 340B oversight void

Sep. 16, 2020
By Mari Serebrov
Given the minimal accountability written into the 340B prescription drug discount program, a few biopharma companies recently began taking oversight into their own hands by demanding data claims or refusing to extend the mandated discounts to contract pharmacies.
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Regulatory front

More than a pledge is needed, CEOs told

Sep. 16, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: DMF a pathway for cannabis drugs.
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Regulatory actions for Sept. 16, 2020

Sep. 16, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: AVM, Cura, Mateon, Mediwound, Orphazyme.
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Canbridge wins approval for MPS II drug and expands partnership with UMass

Sep. 16, 2020
By Elise Mak
BEIJING – Canbridge Pharmaceuticals Inc. last week won marketing approval in China for its first rare disease drug, the mucopolysaccharidosis II therapy Hunterase (idursulfase beta injection).
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Plus Therapeutics’ Rhenium Nanoliposomes are fast tracked in glioblastoma

Sep. 15, 2020
By Lee Landenberger
The FDA has granted Plus Therapeutics Inc. fast track designation for its lead candidate, Rhenium Nanoliposomes (RNL), for treating recurrent glioblastoma, propelling it into the sixth cohort of a phase I dose-finding trial.
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Regulatory front

FDA releases guidance on COVID-19, geriatric labeling, EoE

Sep. 15, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: NIH adds funding to Latino Alzheimer’s research; Sprout warned for Addyi promotion; Scripps to pay $10M over use of NIH grants.
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Regulatory actions for Sept. 15, 2020

Sep. 15, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aerie, Amryt, Apellis, Ardelyx, Astrazeneca, BMS, Boehringer, Epimab, Equillium, Gensight, Gilead, Kiniksa, Lilly, Mateon, Matinas, Novartis, Plus, Takeda, Zynerba.
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