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BioWorld - Friday, June 19, 2026
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Home » Topics » BioWorld, Regulatory

BioWorld, Regulatory
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Regulatory actions for March 21, 2022

March 21, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Astrazeneca, Cstone, Kiora, Moderna, Sobi.
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Marinus wins first nod as FDA clears Ztalmy in rare CDKL5 deficiency disorder

March 18, 2022
By Jennifer Boggs and Lee Landenberger
Marinus Pharmaceuticals Inc.’s GABAA receptor agonist Ztalmy (ganaxolone), has won U.S. FDA approval for treating seizures associated with cyclin-dependent kinase-like 5 (CDKL5) deficiency disorder.
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Regulatory actions for March 18, 2022

March 18, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Abbvie, Amolyt, Aquestive, Bioheng, Heron, Inflarx, Moderna, TC, Tetra.
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Regulatory actions for March 17, 2022

March 17, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Adagene, Aim Immunotech, Biontech, Brii, Iovance, Kaléo, Ossium Health, Pfizer, Shionogi, Sonnet, The AIDS Clinical Trials Group.
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‘Outdated’ COVID-19 IP waiver advances at WTO, while White House seeks more pandemic funding

March 16, 2022
By Jennifer Boggs
With global COVID-19 cases on the rise once again, the World Trade Organization (WTO) said it reached consensus among four WTO members – the U.S., European Union, India and South Africa – for an IP waiver regarding vaccines, a proposal to which biopharma reiterated its objections. Meanwhile, in the U.S., the White House appealed to Congress to provide adequate funding to continue the country’s pandemic response, and Pfizer Inc. and Biontech SE submitted an application to the FDA seeking emergency use authorization for a fourth shot of its COVID-19 vaccine.
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Pills, bottle atop $100 bill

Talk of US Rx pricing reforms mired in déjà vu

March 16, 2022
By Mari Serebrov
When it comes to lowering U.S. drug prices, Congress has a lot of options among the several bills that have been introduced in both the House and Senate over the years. But a deadlock between bipartisan measures and partisan proposals has reduced legislative action to mere talk. The deadlock, and the at times hyperbolic debate, continued in yet another congressional hearing March 16 on “the urgent need to lower drug prices in Medicare,” as the Senate Finance Committee billed it.
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US FDA advises on gene therapies in two draft guidances

March 16, 2022
To advance gene therapies incorporating genetic modifications, the U.S. FDA issued two draft guidances this week.
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Regulatory actions for March 16, 2022

March 16, 2022
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Allarity, Arrowhead, Beigene, Kairos, Maia, Medison, Myrtelle, Pepgen, Quoin, Wesana.
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Eye and DNA

Hansoh wins China’s first approval for an anti-CD19 antibody to treat NMOSD

March 15, 2022
By Doris Yu

Hansoh Pharmaceutical Group Co. Ltd. has won a green light for inebilizumab, approved by China’s NMPA for the treatment of adults with neuromyelitis optica spectrum disorders (NMOSD) who are anti-aquaporin-4 immunoglobulin G (AQP4-IgG) seropositive. The decision marked Hansoh’s first biologic approval.


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Vials, syringes, pills and masks

HELP looks to the future with PREVENT bill

March 15, 2022
By Mari Serebrov
The bipartisan PREVENT Pandemics Act, which seeks to put into U.S. law many of the lessons learned from the COVID-19 pandemic, marked its first milestone March 15, with the Senate Health, Education, Labor and Pensions (HELP) Committee sending it to the full Senate with a do-pass recommendation on a 20-2 vote.
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