Articles
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3 weeks ago |
lupusnewstoday.com | Lindsey Shapiro
People with systemic lupus erythematosus (SLE) who have antibodies that target the mitochondrial transcription factor A (TFAM) protein are more likely to develop certain blood clotting complications, a study found. The antibodies were a risk factor for blood clots, or thrombotic events, even when accounting for other factors that could play a role, such as smoking or the presence of other types of self-reactive antibodies (autoantibodies) linked to SLE.
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3 weeks ago |
lupusnewstoday.com | Lindsey Shapiro
October 23, 2023 by Lindsey Shapiro Lupus Therapeutics to support development of NK cell therapy Lupus Therapeutics will partner with Nkarta to advance the development of NKX019, Nkarta’s investigational natural killer (NK) cell therapy, for people with treatment-resistant lupus nephritis, a serious complication of lupus that features kidney damage and dysfunction. The U.S. Food and Drug Administration (FDA) recently cleared the launch…
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1 month ago |
lupusnewstoday.com | Margarida Maia
May is Lupus Awareness Month, and the Lupus Foundation of America is calling on supporters to join efforts to bring attention to lupus, an autoimmune disease whose symptoms are not always readily apparent. The focus of this year’s awareness month is “Make Lupus Visible” — given that the chronic condition is often invisible to others. For World Lupus Day on May 10, the World Lupus Federation, a global coalition, will also be pushing for greater awareness and more resources for patients.
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1 month ago |
lupusnewstoday.com | Marisa Wexler
The U.S. Food and Drug Administration (FDA) has granted regenerative medicine advanced therapy (RMAT) designation to FT819, a cell therapy Fate Therapeutics is developing to treat lupus. An RMAT designation is awarded to treatments for serious conditions that have shown promise in early clinical testing.
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2 months ago |
lupusnewstoday.com | Patricia Inacio |Steve Bryson |Katherine Poinsatte |Andrea Lobo
The U.S. Food and Drug Administration (FDA) has agreed to review an application by Roche seeking approval of obinutuzumab for the treatment of lupus nephritis, a lupus complication marked by kidney inflammation and damage. Developed by Roche’s subsidiary Genentech and Biogen, obinutuzumab is an antibody-based treatment, already approved for certain blood cancers, that was found in a clinical trial to ease symptoms of kidney disease in lupus nephritis patients.
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