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BioWorld - Monday, July 6, 2026
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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory front

Adcom: ADF offers no meaningful reduction in overall Oxycontin abuse

Sep. 14, 2020
By Mari Serebrov
The latest global regulatory news, changes and updates affecting biopharma, including: FDA advises on getting back to business as usual; ICER evidence report targets ulcerative colitis treatments.
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Regulatory actions for Sept. 14, 2020

Sep. 14, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascentage, Cycle, Essa, Gan & Lee, Gannex, Kiadis, Mateon, Novartis, Pharmacyte, Regeneron, Reven, Sanofi, SK, Seneca, Supernus, Vaxart, Vertex, Ziopharm.
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Regulatory actions for Sept. 11, 2020

Sep. 11, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Appili, Immupharma, Junshi, Seres, Sol-Gel.
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Regulatory actions for Sept. 10, 2020

Sep. 10, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Arch, Genmab, GSK, Halozyme, Sarepta, Terns, Zai Lab.
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Regulatory front

Herd immunity not totally reliant on vaccines

Sep. 10, 2020
By Mari Serebrov
Vaccine hesitancy could slow the development of herd immunity for COVID-19 in the U.S., but there could be other ways to help reach it. Testifying at a Senate Health, Education, Labor and Pensions (HELP) Committee hearing Sept. 9, Surgeon General Jerome Adams said the numbers needed for herd immunity vary from expert to expert, but it ranges from 60% to 80% of the population.
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Regulatory actions for Sept. 9, 2020

Sep. 9, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aldeyra, Apros, Ascendis, Beigene, Biomarin, Canbridge, Moleculin, Nanomab, Peptilogics, Precision, Reneo, Sellas.
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Lung cancer illustration

The RET stuff: Genentech’s newly approved therapy to compete with Lilly’s

Sep. 8, 2020
By Lee Landenberger
The FDA’s approval of Genentech Inc.’s Gavreto (pralsetinib) for treating adults with metastatic rearranged during transfection (RET) fusion-positive non-small-cell lung cancer (NSCLC) follows the FDA’s May approval of Eli Lilly and Co.’s Retevmo for patients whose tumors have a RET alteration. Gavreto will be commercialized in the U.S. by Genentech, part of the Roche Group, along with Blueprint Medicines Corp., which developed the once-daily oral therapy. Outside the U.S., Roche will handle commercialization.
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Regulatory actions for Sept. 8, 2020

Sep. 8, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aft, Arcutis, Aridis, Ascentage, Atara, Athena, Beyondspring, Caribou, Heron, Hyloris, Kadmon, Kleo, LNC, Marinomed, Ocular, Prometic, Protara, Roche, Silence, VBL.
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Regulatory front for Sept. 8, 2020

Sep. 8, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Abbvie, Allergan, Astrazeneca, Calvin Scott, Gedeon Richter, HRA Pharma, Nestle.
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Regulatory actions for Sept. 4, 2020

Sep. 4, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Ascendis, Kite, Lilly.
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