US-based Azurity Pharmaceuticals Inc announced on Tuesday that the US Food and Drug Administration (FDA) has approved XIFYRM (meloxicam injection), an IV non-steroidal anti-inflammatory drug (NSAID) that offers once daily dosing.
XIFYRM is indicated for use in adults for the management of moderate-to-severe pain, alone or in combination with non-NSAID analgesics. XIFYRM provides a non-opioid analgesic in a 30mg/mL vial for IV bolus injection over 15 seconds. Because of delayed onset of analgesia, XIFYRM alone is not recommended for use when rapid onset of analgesia is required.
"XIFYRM demonstrates our commitment to improving patient care by providing an alternate dosage form for pain management," commented Ron Scarboro, Azurity Pharmaceuticals CEO. "XIFYRM addresses an important clinical need, especially for patients requiring a non-opioid component to multimodal analgesia strategies."
Azurity Pharmaceuticals expects XIFYRM to be available in the coming weeks.
SciBase introduces Nevisense pilot at Florida research university
Exact Sciences secures Medicare coverage for Oncodetect MRD test in colorectal cancer
Tyra Biosciences to announce TYRA-300 preclinical results at ENDO 2025
Centivax raises USD45m to commercialise universal flu vaccine
Adcentrx Therapeutics' ADRX-0405 granted US FDA orphan drug designation
Avenzo Therapeutics doses first patient in AVZO-1418/DB-1418 Phase 1/2 clinical study
SCG Cell's SCG101V therapy Investigational New Drug Application receives Chinese regulatory approval
Celltrion USA launches denosumab biosimilars STOBOCLO and OSENVELT (denosumab-bmwo) in US
HotSpot Therapeutics presents small molecule CBM signalosome inhibitor program data
CyanVac's nasal COVID vaccine shows promise in phase 1 trial