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BioWorld - Saturday, June 13, 2026
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Kiniksa reaches commercial stage with first FDA-approved drug for recurrent pericarditis

March 19, 2021
By Jennifer Boggs and Michael Fitzhugh
Barely five and a half years since the company was founded, Kiniksa Pharmaceuticals Ltd. has moved its first drug over the finish line, winning FDA approval for interleukin-1 blocker (IL-1) rilonacept to treat recurrent pericarditis and reduce the risk of recurrence in adults and children 12 and older.
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Regulatory front for March 19, 2021

March 19, 2021
The latest global regulatory news, changes and updates affecting biopharma.
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Regulatory actions for March 19, 2021

March 19, 2021
Regulatory snapshots, including global drug submissions and approvals, clinical trial approvals and other regulatory decisions and designations: BMS, Idorsia, J&J, Kiniksa, RDIF.
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Multiple sclerosis

Can ya, Gilenya? J&J’s Ponvory for MS aims to intervene in sphingosine

March 19, 2021
By Randy Osborne
Now that Johnson & Johnson (J&J), through its Janssen Pharmaceuticals unit, has won the FDA’s nod for Ponvory (ponesimod), market factors will decide how the once-daily oral selective sphingosine-1-phosphate receptor 1 modulator fares against several others already approved in the class.
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FDA approves Arcalyst for recurrent pericarditis

March 19, 2021

Regulatory front for March 18, 2021

March 18, 2021
By Mark McCarty
The latest global regulatory news, changes and updates affecting medical devices and technologies, including: FDA grants de novo for Biofire multianalyte assay; No injuries or deaths associated with Acist Kodama recall; Supreme Court to hear assignor estoppel case; Cardiac rehab bill resurfaces in U.S. House.
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Regulatory actions for March 18, 2021

March 18, 2021
Regulatory snapshots, including global submissions and approvals, clinical trial approvals and other regulatory decisions and designations: Biofire, Boston Scientific, Braintale, Catalyst, Life Spine, Stimdia.
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U.S. FDA headquarters

Is U.S. FDA getting tougher under Biden?

March 18, 2021
By Mari Serebrov
Although U.S. President Joe Biden has yet to nominate his choice to lead the FDA, his nomination of Xavier Becerra as the next Health and Human Services (HHS) secretary – and Becerra’s Senate confirmation March 18 – could signal a shift to a more conservative approach at the FDA when it comes to approving new drugs and devices.
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Astrazeneca-COVID-19-vaccine-vials

EMA review finds benefits outweigh risks for Astrazeneca COVID-19 vaccine

March 18, 2021
By Nuala Moran
LONDON – Astrazeneca plc’s COVID-19 vaccine is safe and effective and the benefits well outweigh any risks, according to a review carried out by the EMA, following reports of blood clots in people who received the vaccine.
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European Commission headquarters

EC launches council to make money out of science

March 18, 2021
By Mari Serebrov
Combining research on emerging technologies with an accelerator program and a dedicated equity fund, the European Commission (EC) launched the European Innovation Council March 18 to invest in promising research and to scale up innovative startups and small- and medium-size businesses.
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