Protein based therapeutics have been regarded very highly as they have produced immense results in treating various diseases including genetic disorders, neurodegenerative disorders, sexually transmitted diseases, and autoimmune disorders. This has revolutionized the field of medicine by enabling precise targeting for treating diseases and personalized medicine for different individuals. The ability to target the source of a disease or disorder has made this line of therapeutics a major outbreak for revolutionizing the field of targeted medicine and is currently being pursued for developing novel therapeutics. The production of recombinant protein paved the way for these therapeutics and despite the considerable progress made so far in the study and production of therapeutic proteins, there are still concerns over its off-target effects and ethical considerations, which have spurred the exploration of alternative approaches. In this context, this article is presented on therapeutic proteins, an innovative biological approach that has the potential to cure disorders that were once considered incurable. This article highlights the limitations of current targeted medicine technologies and the need for more targeted and personalized approaches to treat genetic disorders. Employing artificially synthesized therapeutic proteins such as monoclonal antibodies (MAC) to target specific cells, tissues, organs, genes, proteins, and sites of disease progression has proven to be more effective in treating the diseases. This approach provides greater specificity and control over various disorders, making it a highly promising therapeutic option for various diseases such as cancer, cardiovascular diseases, and viral infections. This article discusses the status of therapeutic proteins, their potential prospects, as well as the challenges and opportunities that need to be addressed to fully exploit their potential. Overall, the article aims to shed light on the significance of therapeutic medicine in the field of medicine and its potential to revolutionize treatments for various disorders. By providing an overview of this innovative approach, it hopes to inspire further research in this area and pave the way for novel and more effective therapies for genetic disorders.

Anti-ageing is an idea that has always been a part of human life. Eternal life and immortality are parts of fantasy which were given a hope to become true with developing technology. Anti-ageing research is being conducted with the hopes of finding ways to improve lifespan, reversing the impacts of certain diseases in humans which leads to cell death and faster progression of aging and to develop regenerative medicine. There are genes in certain species of animals and other organisms which tend to reduce the speed of aging in the organisms, it is also found out that these genes are also present in human beings but are inactive. There are also ways to manipulate these genes and activate them using certain compounds and their activation might prove to be helpful in improving lifespan and curing various diseases which leads to the destruction of cells and their aging. This also helps in regenerative medicine. Gene therapy is one of the developing approaches for almost every disease and their progression which also includes the age-related ones. Gene therapy helps to alter the genome to produce the desired results but when it comes to anti-ageing gene therapy there have been a lot of hindrances like ethical issues, unsatisfactory results of the therapy and side effects so this therapy hasn't been brought into application yet but if the hurdles were overcome, clinical implementation of this technology and with the upcoming CRISPR technology it will give rise to various closed disciplines from the past.