Clinical TrialID 5333
A Study in Healthy Volunteers Comparing Two Different Liquid Formulations of Solifenacin With Each Other and With the Tablet Formulation
NCT01406158
Pharmacokinetics of Solifenacin Succinate|Healthy Volunteers
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Record Fields
Scalar fields from the final clinical_trial record.
- Clinical Trial Id
- 5333
- Evidence Id
- 5333
- Core Evidence Id
- 5333
- Source Clinical Trial Id
- 5319
- Herb2 Clinical Trial Id
- HBCT005319
- Nct Id
- NCT01406158
- Title
- A Study in Healthy Volunteers Comparing Two Different Liquid Formulations of Solifenacin With Each Other and With the Tablet Formulation
- Status
- Completed
- Phase
- Phase 1
- Study Result
- No
- Study Condition
- Pharmacokinetics of Solifenacin Succinate|Healthy Volunteers
- Study Type
- Interventional
- Study Design
- Allocation: RANDOMIZED|Intervention Model: CROSSOVER|Masking: NONE|Primary Purpose:
- Intervention
- DRUG: Solifenacin Succinate Formulation A|DRUG: Solifenacin Succinate Formulation B|DRUG: Solifenacin Succinate
- Intervention Allocation
- Randomized
- Intervention Model
- Crossover
- Intervention Mask
- Intervention Purpose
- Gender
- All
- Age
- Adult
- Enrollment
- 24
- Outcome Measure
- Pharmacokinetic assessment of AUC and maximum concentration (Cmax) through the analysis of blood samples, Up to Day 11
- Sponsor Collaborator
- Astellas Pharma Inc
- Funded By
- INDUSTRY
- Location
- Spaulding Clinical Research, West Bend, Wisconsin, 53095, United States
- Other Id
- 905-CL-080
- Start Date
- 2011-05
- Primary Completion Date
- 2011-07
- Completion Date
- 2011-07
- First Posted
- 2011-08-01
- Results First Posted
- Last Update Posted
- 2011-08-24
- Study Document
- Study Url
- https://clinicaltrials.gov/study/NCT01406158
- Title Cn
- Title En
- A Study in Healthy Volunteers Comparing Two Different Liquid Formulations of Solifenacin With Each Other and With the Tablet Formulation
- Bilingual Status
- semi_complete