Tralokinumab for the treatment of severe, uncontrolled asthma: The ATMOSPHERE clinical development program

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Abstract

Tralokinumab, a fully human IgG4 monoclonal antibody, specifically neutralizes IL-13. The ATMOSPHERE clinical development program comprised four randomized, placebo-controlled clinical trials and an open-label study that aimed to assess the efficacy and safety of tralokinumab for the treatment of severe, uncontrolled asthma. The two pivotal trials (STRATOS 1 and STRATOS 2; NCT02161757 and NCT02194699) evaluated the efficacy and safety of tralokinumab, with STRATOS 1 identifying a subgroup most likely to demonstrate enhanced response to treatment. Further trials have assessed the ability of tralokinumab to reduce oral corticosteroid use (TROPOS; NCT02281357) and determined its mechanistic effects (MESOS; NCT02449473). An open-label study in Japanese individuals (NCT02902809) assessed the long-term safety and tolerability of tralokinumab in this population.

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Panettieri, R. A., Wang, M., Braddock, M., Bowen, K., & Colice, G. (2018). Tralokinumab for the treatment of severe, uncontrolled asthma: The ATMOSPHERE clinical development program. Immunotherapy, 10(6), 473–490. https://doi.org/10.2217/imt-2017-0191

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