Drug Discovery; a Process through Which Potential New Therapeutic Entities (Drugs) Are Identified
Drug discovery is the process through which potential novel
drugs are identified. The process involves many different stages and series of
actions. Typically, it can be divided into four main stages: such as early drug
discovery, pre-clinical phase, clinical phases, & regulatory approval. Despite
advances in biotechnology and understanding of biological systems, drug
discovery is still a lengthy, costly, and difficult process with high attrition
rate of new therapeutic discovery. Drug design is a process of finding new
drugs based on the knowledge of a biological target.
According to Coherent
Market Insights the Drug
Discovery Market Global Industry Insights, Trends, Outlook, and
Opportunity Analysis, 2022-2028.
New insights regarding a disease allow researchers to design
a drug to stop or reverse the effects of the disease. Once a lead compound is
found, pre-clinical phase of drug development begins to determine the efficacy
and safety of the drug. The goal of a pre-clinical drug discovery is to deliver
one or more clinical candidate molecules, each with sufficient evidence of
biological activity to a target relevant to the disease as well as adequate safety
and drug-like properties, so that the drug can be entered into clinical phase (human
trial).
Drug discovery is
the process of identifying chemical entities that have the potential to become
therapeutic agents that are capable of presenting unmet medical needs. Modern
drug discovery involves the identification of screening hits, medicinal
chemistry and optimization of those hits to increase the affinity, efficacy and
potency, selectivity (to reduce potential of side effects), metabolic
stability, and oral bioavailability. Whereas outsourced drug discovery is a
contract-based procedure, which is conducted by the contract research
organizations (CROs).
Drugs are used to prevent, diagnose, treat, and/or relieve
symptoms of the disease, and thereby, there is an increasing demand for drugs,
which in turn increase the practice of drug discovery. However, drugs are
tested on people to make sure they are safe and effective. In the U.S., FDA
thoroughly examine all of the submitted data related to the drug and make a
decision to approve or not to approve it. Moreover, the FDA monitors all drug
and device safety once products are available for use by the public.

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