Is the pharmaceutical industry’s preoccupation with the monotherapy drug model stifling the development of effective new drug therapies?

被引:0
作者
Ian Edwin Cock
机构
[1] Nathan Campus,Environmental Futures Research Institute
[2] Griffith University,School of Environment and Science
[3] Nathan Campus,undefined
[4] Griffith University,undefined
来源
Inflammopharmacology | 2018年 / 26卷
关键词
Combinational therapies; Synergy; Drug repurposing; Complementary therapies; Natural products; Drug repurposing; Traditional medicine;
D O I
暂无
中图分类号
学科分类号
摘要
Drug discovery and development is heavily biased towards the development of monotherapies. Screening, testing, and evaluation of mono-entity drugs are generally much simpler than drug combinations, and are generally easier to get approval from the regulatory authorities for their clinical use. However, monotherapy drugs may not have optimal activity, may have associated toxicities, or may lose activity over time as their target develops resistance. Drug combinations, often developed from existing monotherapies, may have improved efficacy and/or be less toxic. Furthermore, the existing drugs which have lost efficacy due to the development of resistance can often be re-activated by combining them with other chemical entities. Thus, whilst the current climate for drug approval, registration, and clinical use drives the majority of drug development research towards the development of monotherapies, combinations are often a substantial improvement on the original drug. This commentary examines monotherapy and combinational therapy models and discusses the benefits and limitations of each model.
引用
收藏
页码:861 / 879
页数:18
相关论文
共 196 条
[71]  
Hodge S(2009) (Ginger) rhizomes in rat adjuvant-induced arthritis China J Chin Mat Med 9 965-undefined
[72]  
Han P(2014)Pau d-arco activates Nrf2-dependent gene expression via the MEK/ERK-pathway Nat Prod Commun 8 1231-undefined
[73]  
Jang MH(2008)Evaluation of the cyclooxygenase inhibiting effects of six major cannabinoids isolated from Int Immunopharmacol 16 3875-undefined
[74]  
Lim S(2011)NF-κB dependent anti-inflammatory activity of chlorojanerin isolated from Molecules undefined undefined-undefined
[75]  
Han SM(undefined)Anti-inflammatory, pro-apoptotic, and anti-proliferative effects of a methanolic neem ( undefined undefined undefined-undefined
[76]  
Jurenka JS(undefined)) leaf extract are mediated via modulation of the nuclear factor-κB pathway undefined undefined undefined-undefined
[77]  
Khdair A(undefined)Anti-inflammatory effects of red pepper ( undefined undefined undefined-undefined
[78]  
Chen D(undefined)) on carrageenan- and antigen-induced inflammation undefined undefined undefined-undefined
[79]  
Patil Y(undefined)Using epigenetic therapy to overcome chemotherapy resistance undefined undefined undefined-undefined
[80]  
Kim JH(undefined)Frankincense and myrrh suppress inflammation via regulation of the metabolic profiling and the MAPK signalling pathway undefined undefined undefined-undefined