To Demonstrate the Effect of Food on the Bioavailability of Glipizide
The Effect of Food on the Bioavailability of Glipizide
1 other identifier
interventional
18
0 countries
N/A
Brief Summary
To demonstrate the effect of food on the bioavailability of Glipizide.
Trial Health
Trial Health Score
Automated assessment based on enrollment pace, timeline, and geographic reach
participants targeted
Target at below P25 for phase_1 type-2-diabetes
Started Nov 1993
Health score is calculated from publicly available data and should be used for screening purposes only.
Trial Relationships
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Study Timeline
Key milestones and dates
Study Start
First participant enrolled
November 1, 1993
CompletedPrimary Completion
Last participant's last visit for primary outcome
November 1, 1993
CompletedStudy Completion
Last participant's last visit for all outcomes
November 1, 1993
CompletedFirst Submitted
Initial submission to the registry
July 24, 2009
CompletedFirst Posted
Study publicly available on registry
July 27, 2009
CompletedMarch 28, 2017
July 1, 2009
Same day
July 24, 2009
March 27, 2017
Conditions
Outcome Measures
Primary Outcomes (1)
Bioequivalence based on AUC and Cmax
15 days
Study Arms (3)
1
EXPERIMENTAL10 mg Glipizide Tablet (Geneva Pharmaceutical, Inc.), Administered Immediately After a Standard Breakfast.
3
ACTIVE COMPARATOR10 mg Glucotrol Tablet (Roerig), Administered Immediately After a Standard Breakfast.
2
EXPERIMENTAL10 mg Glipizide Tablet (Geneva Pharmaceutical, Inc.), Administered After an Overnight Fast.
Interventions
Eligibility Criteria
You may qualify if:
- No clinically significant abnormal finding on physical exam, medical history, or clinical laboratory results on screening.
You may not qualify if:
- Positive test results for HIV or hepatitis B or C.
- Treatment for drug or alcohol dependence.
Contact the study team to confirm eligibility.
Sponsors & Collaborators
- Sandozlead
MeSH Terms
Conditions
Interventions
Condition Hierarchy (Ancestors)
Intervention Hierarchy (Ancestors)
Study Officials
- PRINCIPAL INVESTIGATOR
Roger D. Anderson, M.D.
Novum Pharmaceutical Research Services
Study Design
- Study Type
- interventional
- Phase
- phase 1
- Allocation
- RANDOMIZED
- Masking
- NONE
- Purpose
- TREATMENT
- Intervention Model
- CROSSOVER
- Sponsor Type
- INDUSTRY
Study Record Dates
First Submitted
July 24, 2009
First Posted
July 27, 2009
Study Start
November 1, 1993
Primary Completion
November 1, 1993
Study Completion
November 1, 1993
Last Updated
March 28, 2017
Record last verified: 2009-07