For patients who rely on monoclonal antibodies and other biologic drugs, treatment often means hours tethered to an IV pole ...

A woman dubbed the “injection aunt,” a figure alleged to have provided off-the-books intravenous drips and prescription drugs ...

A sweeping inspection campaign by the Jordan Food and Drug Administration (JFDA) has uncovered unapproved cosmetic injections being used inside two medical facilities in Amman, prompting immediate ...

Hikma Pharmaceuticals PLC (Hikma), the multinational pharmaceutical company, today announces the launch of the first-of-its-kind, ready-to-use vancomycin premix with room-temperature stability under ...

The U.S. Food and Drug Administration has approved an oral pellet formulation of BioCryst Pharmaceuticals' drug to prevent ...

With Qfitlia and Cablivi, Sanofi reaches its fourth and fifth approvals in China this year, following Tzield for stage 2 type ...

The subcutaneous administration of the established immunotherapy could free up an estimated 30,000 hours of infusion chair ...

Cevostamab demonstrated a 38.8% overall response rate in relapsed/refractory multiple myeloma, with a median response duration of 12.3 months. BCMA-naive patients showed a higher overall response rate ...

Emergent BioSolutions (NYSE: EBS) today announced that the U.S. Food and Drug Administration (FDA) has approved its supplemental Biologics License Application (sBLA) for its Winnipeg, Canada facility ...

Enable Injections is a combination product company that is synonymous with large-volume wearable injectors. When biopharma companies want to make their biologics more convenient for patients, they ...

The approval of Emeprev will help veterinary professionals by providing an in-clinic antiemetic option.