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Find Clinical Drug Pipeline Developments & Deals by UCB Pharma S.A
Bimzelx (bimekizumab) is a humanized IgG1 monoclonal antibody that selectively binds to IL-17A, IL-17F and IL-17AF cytokines. It is approved for the treatment of adults with moderate-to-severe hidradenitis suppurativa.
Bimzelx (bimekizumab) is an IL-17A and IL-17F inhibitor, which is being evaluated for the treatment of adults with moderate-to-severe hidradenitis suppurativa.
Bimzelx (bimekizumab) is a humanized IgG1 monoclonal antibody that selectively binds to IL-17A, IL-17F and IL-17AF cytokines. It is being evaluated for the treatment of adults with moderate-to-severe hidradenitis suppurativa.
Bimzelx (bimekizumab) is a humanized IgG1 monoclonal antibody that selectively binds to IL-17A, IL-17F and IL-17AF cytokines. It is being evaluated for the treatment of adults with moderate-to-severe hidradenitis suppurativa.
The net proceeds will be used to the advancement of novel medicines, including IMB1001, a highly promising humanized antibody targeting CD226, for immune-mediated inflammatory diseases (IMIDs).
Rystiggo (rozanolixizumab) is a humanized IgG4 monoclonal antibody that binds to the neonatal Fc receptor (FcRn) resulting in the reduction of circulating IgG. It is approved by EMA for generalized myasthenia gravis.
Zilbrysq (zilucoplan) is FDA-approved as the first and only self-administered C5 complement inhibitor indicated for the treatment of generalized myasthenia gravis (gMG) in adult patients who are anti-AChR antibody positive.
Zilbrysq (zilucoplan) is a C5 inhibitor peptide drug candidate, which is currently being evaluated for the treatment of patients with AChR antibody-positive generalized myasthenia gravis.
Bimzelx (bimekizumab) is a humanized monoclonal IgG1 antibody that is designed to selectively inhibit both IL-17A and IL-17F, two key cytokines driving inflammatory processes, received positive CHMP opinion for severe plaque psoriasis.
Rystiggo (rozanolixizumab) is an FcRn Binder antibody drug candidate, which is currently being evaluated for the treatment of adult patients with generalized myasthenia gravis.
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