Lokman Hekim Health Sciences
Article Open Access Volume 3 · Issue 3 · 2023 pp. 223–229

The Development, Indications, and the Safety of Monoclonal Antibodies

Hakkı Zafer Güney1 ORCID, Merve Mete2 ORCID, Bilgen Dölek3 ORCID, Murat Yuvakuran4 ORCID, Zehra Mantin5 ORCID
1 Department of Pharmacology, Lokman Hekim University Faculty of Medicine, Ankara, Türkiye
2 Project Manager of Amgen Biotechnology and Gensenta Pharma
3 Director of Market Access, Health Policy and Corporate Affairs, Amgen Türkiye
4 Senior Manager of Market Access , Health Policy, Governmental Affairs, Amgen Türkiye
5 Manager of Market Access , Health Policy, Governmental Affairs, Amgen Türkiye
Published: 2023 DOI: 10.14744/lhhs.2023.12008 Article ID: LHHS-03581
Abstract
Monoclonal antibodies (mAbs) are described as brand-new tools used in the therapy of cancer, autoimmune and infectious diseases, transplant rejection, and some other new indications. MAbs have been shown to create some adverse events such as hypersensitivity reactions, immunological problems, cardiovascular diseases, respiratory events, proteinuria, nephrotoxicity, dermatologic events, and cytopenia. In this review, our purpose is to overview the indications and the unwanted events matched with these drugs and negotiate the developments in the development of these drugs that are able to increase the efficacy and decrease the safety problems.

Keywords: Adverse effect; Cancer molecular biology; Clinical drug studies; Drug development; Monoclonal antibody

Article information

1,878 Views
1,874 Downloads
View / Download PDF

Current Issue Vol 3 · Iss 3

Submit manuscript
Most read & early access
Click an article to open abstract.
View all articles