» Articles » PMID: 20716397

Challenges and Opportunities for Drug Discovery in Psychiatric Disorders: the Drug Hunters' Perspective

Overview
Specialty Psychiatry
Date 2010 Aug 19
PMID 20716397
Citations 35
Authors
Affiliations
Soon will be listed here.
Abstract

Innovation is essential for the identification of novel pharmacological therapies to meet the treatment needs of patients with psychiatric disorders. However, over the last 20 yr, in spite of major investments targets falling outside the classical aminergic mechanisms have shown diminished returns. The disappointments are traced to failures in the target identification and target validation effort, as reflected by the poor ability of current bioassays and animal models to predict efficacy and side-effects. Mismatch between disease biology and how psychiatric diseases are categorized has resulted in clinical trials of highly specific agents in heterogeneous patients, leading to variable treatment effects and failed studies. As drug hunters, one sees the opportunity to overhaul the pharmaceutical research and development (R&D) process. Improvements in both preclinical and clinical translational research need to be considered. Linking pharmacodynamic markers with disease biology should provide more predictive and innovative early clinical trials which in turn will increase the success rate of discovering new medicines. However, to exploit these exciting scientific discoveries, pharmaceutical companies need to question the conventional drug research and development model which is silo-driven, non-integrative across the confines of a company, non-disclosing across the pharmaceutical industry, and often independent from academia. This leads to huge redundancy in effort and lack of contextual learning in real time. Nevertheless, there are signs that drug discovery in the 21st century will see more intentional government, academic and industrial collaborations to overcome the above challenges that could eventually link mechanistic disease biology to segments of patients, affording them the benefits of rational and targeted therapy.

Citing Articles

Identifying neurobiological heterogeneity in clinical high-risk psychosis: a data-driven biotyping approach using resting-state functional connectivity.

Tang X, Wei Y, Pang J, Xu L, Cui H, Liu X Schizophrenia (Heidelb). 2025; 11(1):13.

PMID: 39905003 PMC: 11794858. DOI: 10.1038/s41537-025-00565-6.


What Remains to Be Discovered in Schizophrenia Therapeutics: Contributions by Advancing the Molecular Mechanisms of Drugs for Psychosis and Schizophrenia.

Correll C, Tusconi M, Carta M, Dursun S Biomolecules. 2024; 14(8).

PMID: 39199294 PMC: 11353083. DOI: 10.3390/biom14080906.


Role of Biosynthesis and Catabolism of Neurotransmitters in Drug Discovery for Anxiety and Depression.

Patil A, Koul S Curr Pharm Des. 2024; 30(33):2587-2596.

PMID: 39075953 DOI: 10.2174/0113816128309913240704095334.


Exploring mood disorders and treatment options using human stem cells.

Hudock A, Leal Z, Sharma A, Mei A, Santos R, Marchetto M Genet Mol Biol. 2024; 47Suppl 1(Suppl 1):e20230305.

PMID: 38954533 PMC: 11223183. DOI: 10.1590/1678-4685-GMB-2023-0305.


Identifying plasma metabolic characteristics of major depressive disorder, bipolar disorder, and schizophrenia in adolescents.

Yin B, Cai Y, Teng T, Wang X, Liu X, Li X Transl Psychiatry. 2024; 14(1):163.

PMID: 38531835 PMC: 10966062. DOI: 10.1038/s41398-024-02886-z.