Clinical trial
Randomized, 4-Way Replicate Crossover, Bioequivalence Study of Cabergoline 0.5 mg Tablets and Dostinex 0.5 mg Tablets Administered as 2 x 0.5 mg Tablets in Healthy Adult Females and Males Under Fasting Conditions
NCT00653055 is registered in ClinicalTrials.gov with Par Pharmaceutical, Inc. as lead sponsor.
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Registry record
As filed in ClinicalTrials.gov.
- Title
- Randomized, 4-Way Replicate Crossover, Bioequivalence Study of Cabergoline 0.5 mg Tablets and Dostinex 0.5 mg Tablets Administered as 2 x 0.5 mg Tablets in Healthy Adult Females and Males Under Fasting Conditions
- Lead sponsor
- Par Pharmaceutical, Inc.
- Phase
- Phase 1
- Overall status
- Completed
- Start date
- August 31, 2001
- Completion date
- December 31, 2001
- Enrollment
- 40 (actual)
- Sites
- 1
Conditions
As the registry lists them; a condition with its own page is linked.
to determine bioequivalence under fasting conditions