Clinical trial
A Randomized, Open Label, Two Treatment, Two Period, Two Sequence, Single Dose, Crossover Bioequivalence Study of Fluoxetine Hydrochloride Delayed-Release Capsules 90 mg of Dr. Reddy's and Prozac®Weekly 90 mg DR Capsules of Eli Lilly and Company, USA in Healthy Adult Human Subjects Under Fasting Conditions
NCT01166100 is registered in ClinicalTrials.gov with Dr. Reddy's Laboratories Limited as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- A Randomized, Open Label, Two Treatment, Two Period, Two Sequence, Single Dose, Crossover Bioequivalence Study of Fluoxetine Hydrochloride Delayed-Release Capsules 90 mg of Dr. Reddy's and Prozac®Weekly 90 mg DR Capsules of Eli Lilly and Company, USA in Healthy Adult Human Subjects Under Fasting Conditions
- Lead sponsor
- Dr. Reddy's Laboratories Limited
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- February 28, 2006
- Completion date
- August 31, 2006
- Enrollment
- 54 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
healthy