Expired Study
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San Antonio, Texas 78217


The primary objective of this study is to evaluate the comparative bioavailability of a test product of dronabinol oral solution administered under fed conditions to the reference listed drug (RLD) administered to participants under fed and fasted conditions. The secondary objective is to compare the onset of detectable dronabinol concentrations between dronabinol oral solution and the RLD.


Inclusion Criteria: - Meets protocol-specified criteria for qualification - Fully comprehends and signs the informed consent form, understands all study procedures, and can communicate satisfactorily with the Investigator and study coordinator Exclusion Criteria: - History or current use of over-the-counter medications, dietary supplements, or drugs outside protocol-specified parameters - Signs, symptoms or history of any condition that, per protocol or in the opinion of the investigator, might compromise: 1. the safety or well-being of the participant or study staff 2. the safety or well-being of the participant's offspring (such as through pregnancy or breast-feeding) 3. the analysis of results



Primary Contact:

Study Director
Neha Parikh
INSYS Therapeutics Inc

Backup Contact:


Location Contact:

San Antonio, Texas 78217
United States

There is no listed contact information for this specific location.

Site Status: N/A

Data Source: ClinicalTrials.gov

Date Processed: January 21, 2020

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