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BioWorld - Wednesday, February 11, 2026
Home » Topics » Inflammatory, BioWorld

Inflammatory, BioWorld
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Australia’s Cynata ahead of the pack as it progresses iPSCs to phase III osteoarthritis trial

June 24, 2020
By Tamra Sami
PERTH, Australia – Melbourne-based regenerative medicine company Cynata Therapeutics Ltd. is gearing up to take its Cymerus mesenchymal stem cell (MSC) product candidate, CYP-004, into a phase III trial in osteoarthritis.
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Catching up with EMA, FDA grants Ilaris new Still's disease indication

June 17, 2020
By Michael Fitzhugh
Four years after the EMA first approved Novartis AG's Ilaris (canakinumab) for the treatment of adult-onset Still’s disease (AOSD), the FDA has followed suit, giving it a green light in the indication following a priority review. The rare rheumatic condition usually affects younger adults and can occur as infrequently as once, but also intermittently or chronically.
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Seikagaku, Ono Pharma plan next steps for arthritis drug after positive Japan phase III results

June 16, 2020
By Gina Lee
HONG KONG – Japan’s Seikagaku Corp. is contemplating the next move for its ONO-5704/SI-613 (diclofenac etalhyaluronate), a treatment for arthritis that it is co-developing with fellow Japanese company Ono Pharmaceutical Co. Ltd.
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Selecta and Sobi cut a $730M deal for chronic refractory gout

June 12, 2020
By Lee Landenberger
Selecta Biosciences Inc., of Watertown, Mass., and Stockholm’s Swedish Orphan Biovitrum AB (Sobi) signed a licensing agreement for SEL-212, which is designed to control serum uric acid, reduce immunogenicity and allow for repeated monthly dosing when treating chronic refractory gout.
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Foot pain

Near-term rout in gout bout? Wager placed in Selecta, Krystexxa perfecta

May 7, 2020
By Randy Osborne
CEO Carsten Brunn said Selecta Biosciences Inc. has “not seen a material impact” from the COVID-19 pandemic and remains on track to report in the third quarter phase IIb data from a head-to-head trial comparing its refractory gout candidate, SEL-212, with Krystexxa (pegloticase), from Horizon Therapeutics plc, of Dublin.
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Kolon Tissuegene’s Invossa gets second chance as FDA removes clinical hold

April 16, 2020
By Gina Lee
HONG KONG – South Korean biopharmaceutical company Kolon Tissuegene Inc. got a new lease on life as the U.S. FDA lifted the hold on the phase III trial for its lead candidate, Invossa-K (Invossa), for the treatment of osteoarthritis.
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Lungs, COVID-19 test tube, health care worker in PPE

Australia’s Mesoblast plans to evaluate its stem cell therapy in patients infected with COVID-19

March 11, 2020
By Tamra Sami
PERTH, Australia – Australian stem cell therapy company Mesoblast Ltd. plans to evaluate its allogeneic mesenchymal stem cell (MSC) candidate, remestemcel-L, in patients with acute respiratory distress syndrome (ARDS) caused by coronavirus (COVID-19) in the U.S., Australia, China and Europe.
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Bridge Biotherapeutics taps Atomwise in potential $1B AI-based discovery deal

March 10, 2020
By Michael Fitzhugh
South Korea's Bridge Biotherapeutics Inc. has enlisted San Francisco-based AI drug discovery shop Atomwise Inc. to help it identify up to 13 small-molecule inhibitors of Pellino proteins and other targets in an effort to develop new therapies for inflammatory diseases. Atomwise stands to receive an up-front payment of undisclosed value, as well as milestone and royalty payments under terms of the deal. Presuming success, it estimates the partnership's payoff could reach up to $1.08 billion.
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Scorpio maurus palmatus

(Scorpion) Venom a-Blaze: arthritis, brain cancer superhero?

March 6, 2020
By Anette Breindl
In the Marvel Comic Universe, Venom is a superhero who started life as a supervillain and Spiderman foe. In the biopharma universe, scorpion venom is undergoing the same fate transformation, as separate papers this week reported new ways to use scorpion venom in two major therapeutic targeting challenges.
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Inflammatory/Immune: Filgotinib

Filgotinib looks to JAK up sales with multiple indications

Feb. 10, 2020
By Brian Orelli
Filgotinib (GLPG-0634) has the potential to be a blockbuster drug, according to Cortellis Drugs to Watch analysis, but it may take a few approvals in various indications to reach the coveted mark of $1 billion in annual sales.
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