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BioWorld - Sunday, February 15, 2026
Home » Topics » Regulatory, BioWorld

Regulatory, BioWorld
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FDA Approved stamp

Wall Street faithful as Novartis’ two-timing Leqvio enters LDL-C fray

Dec. 27, 2021
By Randy Osborne
Novartis AG’s FDA go-ahead for Leqvio (inclisiran), the first and only small interfering RNA therapy to lower LDL-C, “should come as a relief, given fears that the pandemic could again limit FDA's ability to conduct manufacturing-site inspections,” Jefferies analyst Peter Welford said. PCSK9-targeting Leqvio’s Dec. 22 approval, which came slightly ahead of the Jan. 1, 2022, PDUFA date, landed after a complete response letter about a year ago, citing unresolved facility inspection-related conditions. The drug is dosed twice per year, unlike competitors in the space.
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Regulatory actions for Dec. 27, 2021

Dec. 27, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Accutar, Aimmune, Allarity, Alnylam, Arcutis, Bioarctic, Celularity, Daiichi, Eisai, Fluoguide, GSK, I-Mab, Innovent, Irlab, Lion, Merck, Novartis, Radius, Syndax.
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Former Harvard researcher with undisclosed China contracts found guilty

Dec. 22, 2021
By Mari Serebrov
A U.S. federal jury convicted Charles Lieber, the former chair of Harvard University’s chemistry and chemical biology department, on charges related to lying to federal authorities about his affiliation with China’s Thousand Talents Plan and the Wuhan University of Technology (WUT), as well as failing to report the income he received from the institute.
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Pharmaceutical manufacturing

Pressure continues for vaccine producers to increase supply

Dec. 22, 2021
By Mari Serebrov
With Omicron spreading rapidly, U.S. COVID-19 vaccine producers are facing increasing pressure to up their production and to do more to ensure their vaccines are accessible globally.
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European Union flag, coins

EU moves 15% minimum effective tax rate toward reality

Dec. 22, 2021
By Mari Serebrov
The EU is on its way to becoming one of the first to implement a historic global tax reform agreement, setting a minimum effective tax rate of 15% for large multinational groups, including biopharma and med-tech companies.
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Antengene receives China’s first approval for oral exportin 1 inhibitor

Dec. 22, 2021
By Doris Yu
Antengene Corp. Ltd. received marketing approval from China’s NMPA for ATG-010 (selinexor), a drug that was in-licensed from Karyopharm Therapeutics Inc. It was approved for use in combination with dexamethasone to treat adults with relapsed or refractory multiple myeloma, specifically those who have received prior therapies and whose disease is refractory to at least a proteasome inhibitor, an immunomodulatory agent and an anti-CD38 monoclonal antibody.
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Regulatory actions for Dec. 22, 2021

Dec. 22, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Acadia, Amgen, Aquestive, Astrazeneca, Biontech, Biogen, Cstone, Deciphera, Eli Lilly, Gilead, Helsinn, Hepion, Hoth, Janssen, Lianbio, Mind, Novavax, Northwest, Pfizer, Sandoz, Sol-Gel, Takeda, Vaxine, Viiv, Zogenix.
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Abbvie U.S. headquarters

Abbvie attempts to fight off unlicensed Humira competition

Dec. 21, 2021
By Mari Serebrov
With licensed Humira (adalimumab) biosimilar competition a little more than a year away in the U.S., Abbvie Inc. is trying to fend off competitors that have not signed an agreement with the North Chicago-based company.
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US can now rely on stable supply of critical medical isotope

Dec. 21, 2021
By Mari Serebrov
The U.S. hit a milestone this week in ensuring a stable domestic supply of molybdenum-99 (Mo-99), a medical isotope critical to radiopharmaceuticals that are used in more than 40,000 diagnostic procedures in the U.S. each day.
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Document illustration

US SEC: More risk disclosure needed from China-based companies

Dec. 21, 2021
By Mari Serebrov
Citing recent events that highlighted the risks of investing in companies based in China or that have the majority of their operations there, the U.S. SEC’s Division of Corporation Finance is seeking more specific disclosures from those companies about the legal and operational risks of investing in their securities.
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