Developing Novel Anticancer Drugs for Targeted Populations: An Update
Tadesse B Tafesse1, Mohammed H Bule1, Fazlullah Khan2
1Department of Medicinal Chemistry, School of Pharmacy, Drug Design and Development Research Center and The Institute of Pharmaceutical Sciences, Tehran University of Medical Sciences, Tehran, Iran.
Background:
Due to higher failure rates, lengthy time and high cost of the traditional de novo drug discovery and development process, the rate of opportunity to get new, safe and efficacious drugs for the targeted population, including pediatric patients with cancer, becomes sluggish.
Objectives:
This paper discusses the development of novel anticancer drugs focusing on the identification and selection of targeted anticancer drug development for the targeted population.
Methods:
Information presented in this review was obtained from different databases, including PUBMED, SCOPUS, Web of Science, and EMBASE. Various keywords were used as search terms.
Results:
The pharmaceutical companies currently are executing drug repurposing as an alternative means to accelerate the drug development process that reduces the risk of failure, time and cost, which take 3-12 years with almost 25% overall probability of success as compared to de novo drug discovery and development process (10- 17 years) which has less than 10% probability of success. An alternative strategy to the traditional de novo drug discovery and development process, called drug repurposing, is also presented.
Conclusion:
Therefore, to continue with the progress of developing novel anticancer drugs for the targeted population, identification and selection of target to specific disease type is important. Considering the aspects of the age of the patient and the disease stages such as each cancer types are different when we study the disease at a molecular level. Drug repurposing technique becomes an influential alternative strategy to discover and develop novel anticancer drug candidates.
Insights
Drug repurposing accelerates the development of novel anticancer drugs, offering a faster and more cost-effective alternative to traditional de novo discovery. This strategy enhances the success rate for targeted cancer therapies.
Area of Science:
- Oncology
- Pharmacology
- Drug Development
Background:
- Traditional de novo drug discovery is lengthy, costly, and has high failure rates, slowing the delivery of new cancer drugs.
- Pediatric cancer patients face particular challenges in accessing novel, safe, and effective treatments.
Purpose of the Study:
- To explore the development of novel anticancer drugs.
- To focus on identifying and selecting targeted drug development strategies for specific patient populations.
Main Methods:
- A comprehensive literature review was conducted.
- Databases searched included PubMed, SCOPUS, Web of Science, and EMBASE using various keywords.
Main Results:
- Drug repurposing is an alternative strategy that significantly reduces development time (3-12 years) and cost compared to de novo discovery (10-17 years).
- Drug repurposing offers a higher probability of success (approx. 25%) compared to de novo discovery (less than 10%).
Conclusions:
- Identifying and selecting specific molecular targets is crucial for advancing novel anticancer drug development.
- Drug repurposing is an influential strategy for discovering and developing new anticancer drug candidates, considering patient age and disease stage.
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