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BioWorld - Wednesday, June 24, 2026
Home » Topics » Regulatory

Regulatory
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Benlysta approved as the first therapy for adult patients with active lupus nephritis in the U.S.

Dec. 18, 2020

Macrogenics wins first FDA approval; margetuximab cleared for HER2-positive breast cancer

Dec. 17, 2020
By Jennifer Boggs
Macrogenics Inc., which started the year with a pipeline prioritization, ends 2020 with its first FDA approval. The agency cleared its HER2-targeting Fc-engineered monoclonal antibody margetuximab in combination with chemotherapy for use in patients with metastatic HER2-positive breast cancer who have received two or more prior anti-HER2 regimens, at least one of which was for metastatic disease.
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COVID-19 mRNA vaccine vials, syringe

Moderna vaccine gains FDA adcom support, suggesting EUA likely

Dec. 17, 2020
By Michael Fitzhugh
As expected, the FDA's Vaccines and Related Biological Products Advisory Committee voted near-unanimously on Dec. 17, with one abstention, that available evidence shows the benefits of Moderna Inc.'s COVID-19 vaccine, mRNA-1273, outweigh its risks for people 18 and older. The vote bolsters the likelihood that the regulator will grant the vaccine an emergency use authorization (EUA), which could come as soon as Friday. Not the same as an approval, the authorization would allow for the vaccine's use for the prevention of COVID-19 in the U.S. even as further trials and regulatory evaluation remains underway ahead of a company BLA submission.
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Exero sensor

Exero secures FDA breakthrough designation for GI smart sensor

Dec. 17, 2020
By Annette Boyle
The U.S. FDA granted a breakthrough device designation to Exero Medical Ltd.’s implantable smart sensor for early detection of anastomotic leaks after gastrointestinal (GI) surgery. The device continuously monitors the GI tract near the surgical site to alert providers about potentially deadly leaks.
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Binaxnow COVID-19 Ag Card Home Test

Abbott’s Binaxnow COVID-19 rapid test authorized for home use

Dec. 17, 2020
By Meg Bryant
As COVID-19 cases surge across the U.S., there is growing demand for greater access to testing to rein in the pandemic. On Wednesday, the U.S. FDA granted an emergency use authorization (EUA) to Abbott Laboratories for at-home use of the company’s Binaxnow COVID-19 Ag Card Home Test. Abbott has teamed up with Miami-based telehealth provider Emed to distribute and administer the tests, with an expected 30 million in the first quarter of 2021.
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Regulatory actions for Dec. 17, 2020

Dec. 17, 2020
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Concept Medical, Corvion, Miach Orthopedics.
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Regulatory front for Dec. 17, 2020

Dec. 17, 2020
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for Dec. 17, 2020

Dec. 17, 2020
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Allovir, Amgen, Avenue, Biosight, Blueprint, CNS, Cook Myosite, Decibel, Eton, GSK, Histogen, Kiromic, Macrogenics, Merck, Moleculin, Sigilon, Tarsier, Therapeutic Solutions, Vyne, Zynerba.
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FDA approves Margenza for pretreated metastatic HER2-positive breast cancer

Dec. 17, 2020
Osteoboost vibration belt

FDA breakthrough device designation strengthens Osteoboost outlook

Dec. 16, 2020
By Annette Boyle
Bone Health Technologies Inc. may be on the verge of upstaging a common drug therapy, but don't tell them to break a leg. The San Francisco-based company's Osteoboost Vibration Belt received a U.S. FDA breakthrough designation for technology that delivers gentle stimulation to reduce bone loss and prevent osteoporosis with the goal of reducing the number of potentially devastating broken bones in the elderly.
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