Skip to main content
OpenTrials
Completed

NCT Number: NCT00865670

To Demonstrate the Relative Bioavailability of Azithromycin 600 mg Tablets Under Fed Conditions

To demonstrate the bioequivalence of Azithromycin 600 mg Tablets Under Fed Conditions.

Completed

Looking for future studies?

Notify Me

Key information

Conditions

Age range

19 year–55 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening

Exclusion criteria

  • Positive test results for HIV or hepatitis B or C
  • Treatment for drug or alcohol dependence
  • Female subjects who are pregnant or lactating

Treatment and study plan

Azithromycin Monohydrate 600 mg Tablets

Drug

Zithromax (azithromycin dihydrate) 600 mg Tablets

Drug

Primary outcomes

  1. Bioequivalence according to US FDA guidelines

    Time frame: 32 days

Sponsors and collaborators

Lead sponsor

Sandoz

Industry

Registry information

Official study title

Comparative, Randomized, Single-Dose, 2-way Crossover Bioavailability Study of Geneva 600 mg Azithromycin Monohydrate Tablets and Pfizer Inc. (Zithromax) 600 mg Azithromycin Dihydrate Tablets in Healthy Adult Volunteers Under Fed Conditions

Important dates

Study start
2003
Primary completion
2003
Study completion
2003
First posted
Mar 19, 2009
Registry last updated
Mar 29, 2017

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

Published trials that share one or more normalized conditions with this study.