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Bioequivalency Study of Zidovudine Under Fasting Conditions

NCT00602550·1 site·ClinicalTrials.gov

What this study is about

Take this into the appointment.

Saves the questions and what to expect into your notes, next to the visit they belong to.

Keep this study

Lead

Roxane Laboratories

Age

18–45

Sex

ALL

Healthy volunteers

Accepted

You may be eligible if

No clinically significant abnormal findings on physical exam, medical history, or clinical laboratory findings during screening.

You may not be if

Allergic or adverse responses to zidovudine or any other comparable or similar products.
Participation in clinical trial within 30 days of study initiation.
Positive blood screen for HIV, Hepatitis B and C.

The record

StatusCompleted

PhaseNo phase

Taking part52

StartedJun 2003

UpdatedJan 23, 2018

Conditions

Where1

CEDRA Clinical Research
Austin, Texas, United States

Clareo Health | Bioequivalency Study of Zidovudine Under Fasting Conditions