Upadacitinib Application for Active Psoriatic Arthritis Submitted for Review
AbbVie has submitted an application to the FDA for review of upadacitinib in the treatment of active psoriatic arthritis (PsA) in adults.
AbbVie has submitted an application to the FDA for review of upadacitinib in the treatment of active psoriatic arthritis (PsA) in adults.
The FDA has granted Orphan Drug designation to TLY012 for the treatment of systemic sclerosis.
Use of hydroxychloroquine or chloroquine may increase the risk of ventricular arrhythmia and death in patients hospitalized.
The NDA for voclosporin has been submitted to the Food and Drug Administration (FDA) for the treatment for lupus nephritis.
Biota Biosciences announced the voluntary recall of CBD Complex, Curcumin Complex, and Cannabidiol + Curcumin Injectables due to the products being marketed without the approval of the FDA.
A sBLA has been submitted ot the FDA for golimumab for the treatment of polyarticular juvenile idiopathic arthritis and juvenile PsA in combination with methotrexate.
Novartis will make its hydroxychloroquine intellectual property available to support broad access for the treatment if it is approved for COVID-19.
The FDA has granted Fast Track designation to telitacicept for the treatment of systemic lupus erythematosus.
Perrigo announced that the FDA has approved the abbreviated New Drug Application for its over-the-counter diclofenac sodium topical gel 1% for the temporary relief of arthritis pain in the hand, wrist, elbow, foot, ankle or knee in adults ≥18 years old.
The FDA announced that it is working closely with other government agencies and academic centers to investigate the potential use of chloroquine for the treatment of coronavirus disease 2019 (COVID-19).