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LUPKYNIS® (voclosporin) Achieved Significantly Higher Renal Response in Lupus Nephritis Patients with High Proteinuria Compared to Patients Treated with MMF and Low Dose Steroids Alone

Aurinia Pharmaceuticals Inc. today announced the results of a post-hoc, pooled analysis of the Phase 2 AURA-LV and Phase 3 AURORA 1 studies, which found that LUPKYNIS® with mycophenolate... | June 1, 2023
United States Emily Littlejohn Greg Keenan Aurinia Pharmaceuticals European Congress Aurinia Pharmaceuticals Inc

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Jazz Pharmaceuticals plc: Jazz Pharmaceuticals Demonstrates Continued Leadership in Sleep Medicine with New Data Presentations at SLEEP 2023

Seven abstracts emphasize Jazz's commitment to advancing the care and understanding of debilitating sleep disorders such as narcolepsy and idiopathic hypersomnia DUBLIN, May 31, 2023 /PRNewswire/
United States Andrean Flynn Kelvin Tan Kristin Bhavnani International Classification Of Sleep Disorders Drug Administration

Axsome Therapeutics to Present Data and Post-Hoc Analyses on Auvelity® and Sunosi® at the 2023 American Society of Clinical Psychopharmacology (ASCP) Annual Meeting

Data on Auvelity demonstrating improved functioning in major depressive disorder Data on Sunosi demonstrating improved cognitive function in patients with excessive daytime sleepiness associated with... | May 30, 2023
United States New York Gregory Mattingly Rakesh Jain Eileen Leary Andrew Cutler

FDA approves first drug to treat agitation symptoms associated with dementia due to Alzheimer's disease

This month, the U.S. Food and Drug Administration announced the supplemental approval of Rexulti (brexpiprazole) oral tablets for the treatment of agitation associated with dementia due to Alzheimerโ€™s disease.
United States Tiffany Farchione Division Of Psychiatry Lundbeck Inc Otsuka Pharmaceutical Company Ltd Drug Administration

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