14.Durno N, et al. Biologics and oral systemic treatment preferences in patients and physicians for moderate-to-severe atopic dermatitis: a discrete choice experiment in the United Kingdom and Germany. J Derm Treatment. 2024;35 ( 1 ) . doi: 10.1080/09546634.2024.2417966 15.Penton H, et al....
14.Durno N, et al. Biologics and oral systemic treatment preferences in patients and physicians for moderate-to-severe atopic dermatitis: a discrete choice experiment in the United Kingdom and Germany. J Derm Treatment. 2024;35(1). doi: 10.1080/09546634.2024.2417966 15.Penton H, et al. Asses...
On December 2, 2024, Johnson & Johnson announced submission of 2 supplemental Biologics License Applications (sBLAs) to the FDA for guselkumab (Tremfya) to treat moderate-to-severe psoriasis in children aged 6 and older and active juvenile PsA (jPsA) in those aged 5 and older. Guselkumab, an...
Biologics License Application for Nemolizumab Accepted by FDA for Prurigo Nodularis, Atopic Dermatitis On February 19, 2024, Galderma announced the of its BLA for nemolizumab for the treatment of prurigo nodularis and for adolescents and adults with moderate to severe atopic dermatitis. According t...
Comparative studies have investigated the different biologics, with in vitro studies suggesting that lebrikizumab exhibits a higher binding affinity and slower rate of dissociation than tralokinumab. Another study indirectly comparing lebrikizumab and dupilumab in patients with moderate-to-...
14.Durno N, et al. Biologics and oral systemic treatment preferences in patients and physicians for moderate-to-severe atopic dermatitis: a discrete choice experiment in the United Kingdom and Germany. J Derm Treatment. 2024;35(1). doi: 10.1080/09546634.2024.2417966 ...
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Billed as the first FDA approved biologic to target interleukin (IL)- 4 and 13 inhibitor, dupilumab has carved a a role for itself in multiple conditions as trial after trial have elucidated its role in the management of type 2 inflammation among those with atopic or allergic conditions. The...
Published on:September 27, 2024 Tim Smith This approval by the FDA follows positive findings from the pivotal BOREAS and NOTUS trials on adults with uncontrolled COPD. Advertisement Advertisement
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