The US Food and Drug Administration (FDA) has accepted for review the resubmission of the supplemental biologics license application (sBLA) for Dupixent (dupilumab) to treat adults and pediatric ...

Recently, news portal Malaysiakini released three pieces of “evidence” from a whistleblower, alleging that the government was involved in abuse of power and corruption. In one of the clips, Sindumin ...

The sNDA was submitted to support full approval of OCA for this indication based on data from the COBALT trial, as well as real-world evidence.

Boston College quarterback Thomas Castellanos will enter the transfer portal after being benched this week, On3 Sports ...

The FDA informed Intercept that it is unable to approve the sNDA in its current form, consistent with the outcome of the Gastrointestinal Drugs Advisory Committee (GIDAC) meeting in September 2024. In ...

The FDA in 2016 granted accelerated approval to the FXR agonist as a second-line treatment for adults with PBC, either in ...

Recently the U.S. Food and Drug Administration (FDA) issued updated safety warnings for all glucagon-like peptide 1 receptor ...

In the 2022-23 preseason poll, LSU was eighth and finished the season last. McMahon said the advent of the transfer portal ...

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The Food and Drug Administration (FDA) has expanded a recall of Dynacare-brand baby powder, manufactured by the Dynarex Corporation, due to potential asbestos contamination. Recent tests have ...

The FDA officially deemed the nearly two-year shortage ... Welch logged into his wholesaler portal and was surprised to see "zero allocation" for Mounjaro and Zepbound, meaning he was still ...

Pfizer Inc. (NYSE: PFE) announced today that the U.S. Food and Drug Administration (FDA) has approved ABRYSVO ® (Respiratory Syncytial Virus Vaccine), the company's bivalent RSV prefusion F (RSVpreF) ...