Trial · NCT00829309
Pravastatin 80 mg Tablets Dosed in Healthy Subjects Under Non-Fasting Conditions
NCT00829309, Phase 1, Completed, Teva Pharmaceuticals USA; results first posted 2009-08-18
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Pravastatin 80 mg Tablets Dosed in Healthy Subjects Under Non-Fasting Conditions. Trials, record NCT00829309. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT00829309
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Pravastatin 80 mg Tablets Dosed in Healthy Subjects Under Non-Fasting Conditions
- NCT number
- NCT00829309
- Status
- Completed
- Phases
- Phase 1
- Enrollment
- 16 participants, actual
- Lead sponsor
- Teva Pharmaceuticals USA
- Conditions
- Healthy
- Interventions
- Pravastatin, Pravastatin
- First posted
- 2009-01-27
- Last updated
- 2024-08-20
- Results first posted
- 2009-08-18
Source ClinicalTrials.gov
Registered outcomes3
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Cmax - Maximum Observed Concentration - Pravastatin in Plasma | Blood samples collected over 16 hour period | Bioequivalence based on Cmax |
| Primary | AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) | Blood samples collected over 16 hour period | Bioequivalence based on AUC0-inf |
| Primary | AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) | Blood samples collected over 16 hour period | Bioequivalence based on AUC0-t |
Source ClinicalTrials.gov
Outcomes3
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
| Type | Outcome | Time frame | Population | Units | Measured as |
|---|---|---|---|---|---|
| PRIMARY | Cmax - Maximum Observed Concentration - Pravastatin in Plasma | Blood samples collected over 16 hour period | Data from all subjects who completed the study were included in the statistical analysis. | ng/mL | MEAN |
| PRIMARY | AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) | Blood samples collected over 16 hour period | Data from all subjects who completed the study were included in the statistical analysis. Data from one subject could not be included in the AUC0-inf calculation for Pravachol®. | ng*h/mL | MEAN |
| PRIMARY | AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) | Blood samples collected over 16 hour period | Data from all subjects who completed the study were included in the statistical analysis. | ng*h/mL | MEAN |
Source ClinicalTrials.gov
Results by group6
Each measurement the trial posted, group by group, in the words and numbers it posted.
| Outcome | Group | Category | Value | Spread | Units |
|---|---|---|---|---|---|
| Cmax - Maximum Observed Concentration - Pravastatin in Plasma | Pravastatin | 126.69 | Standard Deviation 60.95 | ng/mL | |
| Cmax - Maximum Observed Concentration - Pravastatin in Plasma | Pravachol® | 130.64 | Standard Deviation 58.86 | ng/mL | |
| AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) | Pravastatin | 273.32 | Standard Deviation 116.86 | ng*h/mL | |
| AUC0-inf - Area Under the Concentration-time Curve From Time Zero to Infinity (Extrapolated) | Pravachol® | 299.56 | Standard Deviation 121.83 | ng*h/mL | |
| AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) | Pravastatin | 241.29 | Standard Deviation 104.11 | ng*h/mL | |
| AUC0-t - Area Under the Concentration-time Curve From Time Zero to Time of Last Non-zero Concentration (Per Participant) | Pravachol® | 251.86 | Standard Deviation 111.26 | ng*h/mL |
Source ClinicalTrials.gov
Participant flow18
How many started, completed or left each group, period by period.
| Period | Milestone | Group | Participants | Units counted |
|---|---|---|---|---|
| First Intervention | STARTED | Pravastatin (Test) First | 8 | |
| First Intervention | STARTED | Pravachol® (Reference) First | 8 | |
| First Intervention | COMPLETED | Pravastatin (Test) First | 8 | |
| First Intervention | COMPLETED | Pravachol® (Reference) First | 8 | |
| First Intervention | NOT COMPLETED | Pravastatin (Test) First | 0 | |
| First Intervention | NOT COMPLETED | Pravachol® (Reference) First | 0 | |
| Washout: 7 Days | STARTED | Pravastatin (Test) First | 8 | |
| Washout: 7 Days | STARTED | Pravachol® (Reference) First | 8 | |
| Washout: 7 Days | COMPLETED | Pravastatin (Test) First | 7 | |
| Washout: 7 Days | COMPLETED | Pravachol® (Reference) First | 8 |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 participant flowAdverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
Papers0
The papers the trial lists on ClinicalTrials.gov.
None in this release.
Grants0
The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.
None in this release.
Trial comparisons0
Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.
None in this release.
Tests0
The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.
None in this release.
Data dates
The day each source was copied for this release.
Sources 3
- ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
- ClinicalTrials.govNo license stated
- NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
- ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
- ClinicalTrials.govnone stated
- NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)
ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.
For software
Read this trial from software.
The record and each of its lists are JSON, twenty rows a page. No key.
GET https://conductscience.org/api/trials/v1/NCT00829309
GET https://conductscience.org/api/trials/v1/NCT00829309/registered