In today's world, Metelimumab is a topic that has gained great relevance in all areas of society. From its impact on the economy to its influence on people's daily lives, Metelimumab has been the subject of continuous debate and analysis. In this article, we will thoroughly explore the different facets of Metelimumab, examining its origins, its evolution over time, and its impact today. Through interviews with experts in the field and relevant statistical data, we seek to build a clear and complete picture of Metelimumab, delving into its implications and challenges.
| Monoclonal antibody | |
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| Type | Whole antibody |
| Source | Human |
| Target | TGF beta 1 |
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Metelimumab (CAT-192) is a human IgG4 monoclonal antibody that neutralizes TGF beta 1 which had been chosen for further development for the treatment of diffuse cutaneous systemic sclerosis, also known as scleroderma.[1] It was dropped from further development in favour of fresolimumab,[2] which was being developed by Genzyme as of 2006.[3]
Metelimumab was isolated by Cambridge Antibody Technology (CAT) using its phage display technology. In 2000, CAT signed a collaborative deal with Genzyme to further develop TGF beta antibodies.[4][5]
In 2004, CAT and Genzyme revealed that Phase I/II trials of metelimumab for scleroderma showed this antibody to be safe and well tolerated across all dose levels, although no conclusions regarding efficacy of the compound could be made.[6]
Initial trials targeted the skin condition scleroderma[7] but, after some unsuccessful clinical trial results, the product was dropped in favour of fresolimumab,[2] which was being developed by Genzyme as of 2006.[3]
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