Phase 1
Completed N=18
Bioavailability Study Comparing 10 Mg Amlodipine Besylate Orally Disintegrating Tablet (ODT) And 10 Mg Amlodipine Besylate Tablets
Healthy Volunteers
Source: ClinicalTrials.gov NCT01138826 ↗
Enrolled (actual)
18
Serious AEs
0.0%
Results posted
Jul 2011
Primary outcomePrimary: Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0-∞)] — 307.225; 324.324; 330.411 hr*ng/mL
Summary
This study is being performed to determine the bioavailability, or extent of absorption into the body, of a 10 mg amlodipine besylate orally disintegrating tablet (ODT) as compared to the bioavailability of a 10 mg amlodipine besylate (non-ODT) tablet.
Outcome Measures
| Outcome | Result | p-value |
|---|---|---|
| PRIMARY Area Under the Curve From Time Zero to Extrapolated Infinite Time [AUC (0-∞)] |
307.225; 324.324; 330.411 | — |
| PRIMARY AUC From Time Zero to Last Quantifiable Concentration (AUClast) |
275.302; 285.974; 287.035 | — |
| PRIMARY Maximum Observed Plasma Concentration (Cmax) |
5.201; 5.117; 4.952 | — |
| SECONDARY Time to Reach Maximum Observed Plasma Concentration (Tmax) |
8.00; 10.00; 13.00 | — |
| SECONDARY Plasma Decay Half-Life (t1/2) |
44.004; 46.698; 49.869 | — |
Eligibility Criteria
Inclusion Criteria
- Healthy male and/or female subjects (Healthy is defined as no clinically relevant abnormalities identified by a detailed medical history, full physical examination, including blood pressure and pulse rate measurement, 12-lead ECG and clinical laboratory tests).
- Body Mass Index (BMI) of 18 to 26 kg/m2; and a total body weight >50 kg (110 lbs).
Exclusion Criteria
- Evidence or history of clinically significant hematological, renal, endocrine, pulmonary, gastrointestinal, cardiovascular, hepatic, psychiatric, neurologic, or allergic disease (including drug allergies, but excluding untreated, asymptomatic, seasonal allergies at time of dosing).
- A positive urine drug screen.
Data sourced from ClinicalTrials.gov (NCT01138826). Outcome figures and adverse-event rates are extracted automatically from the registry's posted results and are provided for clinician reference, not as a substitute for the primary publication. Informational only — not medical advice.