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The Bioequivalence Study of Acyclovir 800 mg Tablet in Healthy Thai Volunteers Under Fasting Conditions - Trial NCT06228430

Access comprehensive clinical trial information for NCT06228430 through Pure Global AI's free database. This Phase 1 trial is sponsored by International Bio service and is currently Not yet recruiting. The study focuses on Healthy Volunteer. Target enrollment is 40 participants.

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NCT06228430
Phase 1
Not yet recruiting
drug
Trial Details
ClinicalTrials.gov • NCT06228430
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The Bioequivalence Study of Acyclovir 800 mg Tablet in Healthy Thai Volunteers Under Fasting Conditions
A Single Dose, Randomized, Open-label, Two-way Crossover Bioequivalence Study of Generic Acyclovir 800 mg Tablet and Reference Product (ZoviraxTM) in Healthy Thai Volunteers Under Fasting Conditions

Study Focus

Healthy Volunteer

Acyclovir 800 mg Tablet

Interventional

drug

Sponsor & Location

International Bio service

Timeline & Enrollment

Phase 1

Feb 12, 2024

Feb 22, 2024

40 participants

Primary Outcome

Plasma Area Under the Curve (AUC(0 to 36 Hour)) for Acyclovir,Peak Plasma Concentration (Cmax) of Acyclovir

Summary

A Single Dose, Randomized, Open-label, Two-way Crossover Bioequivalence Study of Generic
 Acyclovir 800 mg Tablet and Reference Product (Zovirax™) in Healthy Thai Volunteers under
 Fasting Conditions

ICD-10 Classifications

Healthy person accompanying sick person
Routine general health check-up of armed forces
Persons encountering health services in other circumstances
Persons encountering health services in other circumstances
Person encountering health services in unspecified circumstances

Data Source

ClinicalTrials.gov

NCT06228430

Non-Device Trial