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BioWorld - Thursday, April 9, 2026
Home » Topics » Inflammatory, BioWorld

Inflammatory, BioWorld
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Unity shares untied as osteoarthritis of the knee drug fails phase II test

Aug. 17, 2020
By Michael Fitzhugh
Shares of Unity Biotechnology Inc. (NASDAQ:UBX) fell 66.6% to $4.15 on Aug. 17 after UBX-0101, its one-time lead candidate, failed to best a placebo on an established measure of osteoarthritis pain in a phase II study.
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Sanofi expands protein degrader ambitions with $2.15B Kymera deal

July 13, 2020
By Michael Fitzhugh

The industry's expanding quest for protein degraders grew a little larger on July 9 with Sanofi SA tapping Kymera Therapeutics Inc. to advance two new protein degrader programs, one of which will target IRAK4 in patients with immune-inflammatory diseases and another for an undisclosed target. Each program could yield multiple therapies.


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Patric Stenberg and Roger Franklin

Gesynta raises $21M to test novel mechanism in systemic sclerosis

July 8, 2020
By Cormac Sheridan
DUBLIN – Gesynta Pharma AB raised SEK190 million (US$20.6 million) in new funding to move GS-248, a selective inhibitor of microsomal prostaglandin E synthase-1 (mPGES-1), into a phase IIa trial in systemic sclerosis. The study is due to get underway toward the year end. “It’s going to be in the second half of the fourth quarter,” said Patric Stenberg, CEO of Lund, Sweden-based Gesynta.
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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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