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Ixekizumab is a monoclonal antibody used to treat plaque psoriasis, psoriatic arthritis, and spondyloarthritis by selectively blocking interleukin-17A.
Ixekizumab is a monoclonal antibody used to treat plaque psoriasis, psoriatic arthritis, and spondyloarthritis by selectively blocking interleukin-17A.
Ixekizumab is a biotechnologically produced, humanized monoclonal antibody belonging to the class of biologics. It is marketed under the brand name Taltz® and targets the cytokine interleukin-17A (IL-17A), a key signaling protein of the immune system involved in inflammatory processes. The medication is administered by subcutaneous injection (under the skin) and is approved for adults as well as, in certain cases, children and adolescents.
Ixekizumab has been approved by the European Medicines Agency (EMA) and the U.S. Food and Drug Administration (FDA) for the following conditions:
Ixekizumab binds with high specificity to interleukin-17A (IL-17A), a pro-inflammatory cytokine produced by T helper cells (Th17 cells). IL-17A plays a central role in promoting inflammation and the excessive immune response observed in conditions such as psoriasis and spondyloarthritis. By blocking IL-17A, ixekizumab prevents this signaling molecule from binding to its receptor, thereby interrupting the inflammatory cascade. This leads to a significant reduction in skin inflammation, joint symptoms, and other disease manifestations.
Ixekizumab is administered as a subcutaneous injection using a pre-filled autoinjector pen or pre-filled syringe. The dosing schedule varies by indication:
The injection can be administered by a healthcare professional or, after appropriate training, by the patient at home.
Like all biologics, ixekizumab may cause side effects. Common side effects include:
Less common but more serious side effects include:
Ixekizumab must not be used in patients with:
Prior to initiating treatment, patients should be screened for tuberculosis. Patients should be monitored for signs of infection throughout therapy. Special caution is required in patients with a history of inflammatory bowel disease.
Ixekizumab is generally prescribed when conventional therapies (e.g., methotrexate, ciclosporin, phototherapy) have proven insufficient or are not tolerated. In clinical trials, ixekizumab demonstrated clear superiority over placebo and conventional treatments. A significant proportion of patients achieved complete or near-complete skin clearance (PASI 90 or PASI 100). Treatment is regularly monitored by a physician to assess efficacy and safety.
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