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U.S. v. Actelion - Settlement Agreement - United States …
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Stiftung - Tagesheime Allschwil
WebDec 6, 2024 · By Katie Thomas. Dec. 6, 2024. The drug maker Actelion Pharmaceuticals has agreed to a $360 million settlement stemming from an investigation into whether the company illegally funneled kickbacks ... WebJul 30, 2024 · TITUSVILLE, N.J. – July 30, 2024 – The Janssen Pharmaceutical Companies of Johnson & Johnson announced today that the U.S. Food and Drug Administration (FDA) has approved UPTRAVI ® (selexipag) injection for intravenous (IV) use for the treatment of pulmonary arterial hypertension (PAH, WHO Group I) in adult patients with WHO functional … WebJanssen will provide drug supply for the clinical trials and Extended Access Program, and right of reference to data within the Zavesca New Drug Application (NDA) to support the development of BBDF-101. Lead Product (s): Miglustat, Trehalose API. Therapeutic Area: Genetic Disease Product Name: BBDF 101. Highest Development Status: Preclinical ... dani arroyo