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BioWorld - Thursday, February 19, 2026
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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Regulatory actions for July 8, 2020

July 8, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aclaris, Asieris, Astrazeneca, Biogen, Concert, Cormedix, Croma-Pharma, Eisai, Merck, Talaris.
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Stop sign

Patient death in Cellectis CAR T trial for MM leads to clinical hold

July 7, 2020
By Michael Fitzhugh
Cellectis SA said the FDA has placed a clinical hold on a phase I study of UCART-CS1A, an allogenic CAR T-cell therapy it has been testing in patients with relapsed or refractory multiple myeloma, after one person enrolled in the study died from a case of treatment-emergent cardiac arrest. Cellectis' chief medical officer, Carrie Brownstein, told BioWorld she supported the move, which formalized a decision she'd already taken with her team.
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Regulatory front for July 7, 2020

July 7, 2020
The latest global regulatory news, changes and updates affecting biopharma, including: Esperion, Novartis.
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Regulatory actions for July 7, 2020

July 7, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Aldeyra, Cellectis, Cybrexa, Diffusion, Endo, Mallinckrodt, Neurogene, Novartis, Otonomy, Otsuka, Propeller, Senhwa, Sosei.
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FDA Approved seal

Viiv wins FDA approval for new late-line HIV drug

July 6, 2020
By Michael Fitzhugh
Viiv Healthcare Ltd., late Thursday, won FDA approval for Rukobia (fostemsavir), a gp120-directed attachment inhibitor for the treatment of adults with multidrug-resistant HIV-1 infection failing their current antiretroviral regimen due to resistance, intolerance or safety considerations. The drug was reviewed under FDA's fast track and breakthrough therapy status programs.
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Regulatory actions for July 6, 2020

July 6, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: ADC, Adial, Ascendis, CSL Behring, Daiichi Sankyo, Esperare Foundation, Gilead, Medivir, Mesoblast, Mylan, Napo, Sinovac, Viiv.
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Patents, regulations and tech transfer: Challenges for the biotech sector in LatAm

July 2, 2020
By Sergio Held
CAJICA, Colombia – The Latin American biotech sector is scrambling in the midst of the COVID-19 pandemic, not only in coping with the outbreak, but also in finding the path to the future, while avoiding the pitfalls and looking for new opportunities ahead.
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Japan’s MLWH ends June with string of approvals, looks set for busy 2H 2020

July 2, 2020
By Gina Lee
HONG KONG – Japan’s Ministry of Health, Labour and Welfare (MHLW) ended the first half of 2020 by handing out a flurry of approvals to both domestic and international companies across a wide spectrum of indications.
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Regulatory front for July 2, 2020

July 2, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for July 2, 2020

July 2, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acacia, Beigene, Biophytis Eusa, Geron, Metvital, Mundipharma, Napp, Rhythm.
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