The phase I of research establishes the toxicity of an investigational medication.
A phase I clinical research evaluates a novel treatment's efficacy, safety, adverse effects, ideal dose, and timing. It may also examine the appropriate delivery method for a novel therapy (for instance, oral administration, intravenous infusion, or injection), as well as how the therapy interacts with the body.
The dose is often raised a bit at a time to determine the maximum amount that has no negative side effects or the level of toxicity. Only a limited percentage of people who have not benefitted from prior therapies typically participate in phase I clinical trials. Healthy volunteers are occasionally used. likewise known as a phase 1 clinical study.
To learn more phase I of research, refer
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