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BioWorld - Wednesday, May 20, 2026
Breaking News: Tracking hantavirus across the globeBreaking News: Tracking hantavirus across the globe
Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory actions for April 7, 2020

April 7, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Agenus, Alnylam, Ascentage, Blaze, Immunomedics, Merck.
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Regulatory actions for April 6, 2020

April 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acceleron, BMS, Daiichi, Eisai, GW, Histogen, Hope, Mallinckrodt, Mateon, Mesoblast, Novo Nordisk, Takeda, Tetra, Tracon.
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Regulatory front for April 6, 2020

April 6, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Gilead.
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Regulatory actions for April 3, 2020

April 3, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Cytodyn, Gracell, I-Mab, Iveric, Novan, Revive.
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COVID-19 strikes again: U.S. lawmakers say longer comment periods needed

April 2, 2020
By Mari Serebrov
Given the evolving COVID-19 situation, U.S. House committee chairs are asking the White House Office of Management and Budget (OMB) to direct federal agencies to immediately extend all public comment periods by at least 45 days beyond the end of the declared national emergency, whenever that may be.
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Hydroxychloroquine prescription bottle

Desperation drives shortage of antimalarial drugs used to treat COVID-19

April 1, 2020
By Mari Serebrov
The jury is still out on how much hydroxychloroquine and chloroquine actually help in the treatment or prevention of COVID-19, but desperate times have led desperate health care providers to use the antimalarial drugs to treat patients in desperate need of coronavirus cures.
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FDA accepts Mesoblast’s BLA for pediatric GVHD stem cell therapy under priority review

April 1, 2020
By Tamra Sami
PERTH, Australia –Australian stem cell therapy company Mesoblast Ltd. announced that the FDA has accepted its BLA for priority review for its allogeneic mesenchymal precursor cell therapy, remestemcel-L, for children with acute steroid-refractory graft-vs.-host disease (aGVHD).
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Regulatory front for April 1, 2020

April 1, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Amarin stock plummets on district court’s patent ruling on Vascepa

March 31, 2020
By Lee Landenberger
A U.S. district court in Nevada ruled in favor of two ANDA filers in Amarin Corp. plc.’s patent litigation case regarding its fish oil cardiovascular therapy franchise, Vascepa (icosapent ethyl), increasing the possibility of generics crowding Amarin’s U.S. sales.
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Regulatory front for March 31, 2020

March 31, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Pfizer Healthcare India.
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