EAST HANOVER, N.J., Sept. 30, 2025 -- Novartis announced today that Rhapsido® (remibrutinib) received US Food and Drug Administration (FDA)...
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FDA Approves Rhapsido (remibrutinib) as the First Bruton’s Tyrosine Kinase Inhibitor for Chronic Spontaneous Urticaria Novartis has announced FDA approval of Rhapsido as an oral treatment for adult patients with chronic spontaneous urticaria...
EAST HANOVER, N.J., Sept. 30, 2025 -- Novartis announced today that Rhapsido® (remibrutinib) received US Food and Drug Administration (FDA)...
"FDA Approves KEYTRUDA QLEX" DelveInsight's market intelligence analysis reveals the transformative implications of the FDA's September 19, 2025...
"FDA Approves KEYTRUDA QLEX" DelveInsight's market intelligence analysis reveals the transformative implications of the FDA's September 19, 2025...
Sanofi/Regeneron's Dupixent wins CHMP backing for chronic spontaneous urticaria in the EU, paving the way for expanded treatment options.
MONDAY, Sept. 29, 2025 -- The U.S. Food and Drug Administration has approved Opzelura cream 1.5 percent (ruxolitinib) for children ages 2 to 11 years...
"FDA approved INLURIYO (imlunestrant) by Eli Lilly, on September 25, 2025" The pharmaceutical landscape for metastatic breast cancer treatment has...
"FDA approved INLURIYO (imlunestrant) by Eli Lilly, on September 25, 2025" The pharmaceutical landscape for metastatic breast cancer treatment has...
September 29, 2025 -- Kedrion Biopharma announced today that it has received FDA approval for Qivigy®, a new 10% Immunoglobulin for intravenous...
Updated Date: Fri, 03 Oct 2025 00:00:00 EDT
Updated Date: Fri, 03 Oct 2025 00:00:00 EDT