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AbbVie Adds New Warning To Rinvoq (JAK Inhibitor) Label For Rheumatoid Arthritis
Monday, December 6, 2021 - 7:53am | 415Read More...AbbVie Inc (NYSE: ABBV) announced an update to the U.S. Prescribing Information and Medication Guide for Rinvoq (upadacitinib) for rheumatoid arthritis (RA). The update follows a Drug Safety Communication (DSC) issued in September by the FDA following its final review of the...
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Eli Lilly-Incyte's Rheumatoid Arthritis Drug Gets OK From FDA For Solo Use In Hospitalized COVID-19 Patients
Thursday, July 29, 2021 - 1:37pm | 296Read More...The FDA extended the Emergency Use Authorization (EUA) for Eli Lilly And Co's (NYSE: LLY) and Incyte Corporation's (NASDAQ: INCY) rheumatoid arthritis drug Olumiant (baricitinib) to be used as a sole treatment for hospitalized COVID-19 patients who need...
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Navidea Stock Gains After FDA Grants End Of Phase 2 Meeting To Discuss Rheumatoid Arthritis Program
Thursday, July 15, 2021 - 8:48am | 207Read More...The FDA has granted Navidea Biopharmaceuticals Inc's (NYSE: NAVB) request for an End-of-Phase 2 Type B meeting to discuss its ongoing program in Rheumatoid Arthritis and advancement to the Phase 3 trial. The meeting will take place on September 1 via conference call....
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EC Selects Antibody Therapies, Arthritis Drug As Preferred COVID-19 Meds: Reuters
Tuesday, June 29, 2021 - 3:28pm | 235Read More...The European Commission (EC) picked four antibody treatments and a repurposed Eli Lilly And Co's (NYSE: LLY) rheumatoid arthritis drug for an initial portfolio of preferred medications to treat COVID-19, reports Reuters. The selection of drugs is part of the E.U. Strategy...
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Pfizer's Xeljanz Cuts Incidence Of Death, Respiratory Failure In COVID-19 Patients, Brazilian Study Shows
Thursday, June 17, 2021 - 7:12am | 219Read More...Pfizer Inc (NYSE: PFE) said that its oral rheumatoid arthritis drug Xeljanz (tofacitinib) reduced death or respiratory failure in hospitalized COVID-19 patients with pneumonia in Brazil, meeting the study’s primary goal. Results of the study, which tested the drug in 289 hospitalized...
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Lilly's Olumiant Found to Lower Pain In Late-Stage Rheumatoid Arthritis Trial
Wednesday, June 2, 2021 - 12:06pm | 228Read More...Eli Lilly And Co (NYSE: LLY) has reported posthoc analyses data from the Phase 3 RA-BEAM study that showed Olumiant 4mg (baricitinib) lowered pain and duration of morning joint stiffness in moderate to severe rheumatoid arthritis (RA) patients. Discovered by Incyte Corporation...
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AbbVie's Rinvoq Shows Encouraging Long Term Safety, Efficacy In Rheumatoid Arthritis, Psoriatic Arthritis Patients
Wednesday, June 2, 2021 - 10:02am | 277Read More...AbbVie Inc (NYSE: ABBV) has announced results of an analysis from the Phase 3 SELECT-PsA 2 clinical trial, showing that continuous treatment with Rinvoq (upadacitinib) resulted in sustained improvements in psoriatic arthritis patients who did not respond to disease-modifying anti-...
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Sorrento Reports Encouraging Data From Sofusa-Administered Enbrel In Rheumatoid Arthritis
Thursday, May 20, 2021 - 9:48am | 294Read More...Sorrento Therapeutics Inc (NASDAQ: SRNE) reported positive initial results from the Phase 1B study of its Sofusa Lymphatic Delivery System administering Amgen Inc’s (NASDAQ: AMGN) Enbrel for rheumatoid arthritis. Sofusa delivers biologic therapies through the...
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Biogen, Bio-Thera Ink Licensing Agreement For Development Of Actemra-Based Biosimilar For Rheumatoid Arthritis
Thursday, April 8, 2021 - 11:12am | 239Read More...Biogen Inc (NASDAQ: BIIB) and Bio-Thera Solutions Ltd have entered into a commercialization and license agreement to develop, manufacture, and commercialize BAT1806, a proposed biosimilar referencing Genentech's Actemra (tocilizumab). The anti-interleukin-6 (IL-6) receptor...
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Provention Bio's CEO On Identifying Autoimmune Diseases 'Before It's Too Late'
Tuesday, May 5, 2020 - 11:28am | 953Read More...When it comes to treating chronic, immune-mediated diseases, the standard course is to wait for symptoms before beginning treatment. But by that point, it may be too late for intervention. These diseases can silently do irreversible damage, according to Provention Bio Inc (NASDAQ: PRVB) CEO...
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Regeneron, Sanofi Announce FDA Has Accepted For Review BLA For Sarilumab
Friday, January 8, 2016 - 11:36am | 180Read More...Regeneron Pharmaceuticals Inc (NASDAQ: REGN) and Sanofi SA (ADR) (NYSE: SNY) jointly announced Friday morning that the U.S. Food and Drug Administration has accepted for review the Biologics License Application (BLA) for sarilumab. Regeneron noted that the BLA for sarilumab contains data from...











