Drug-drug Interaction Study in Healthy Male Volunteers Following the Administration of Pantoprazole and Rosuvastatin
Overview[ - collapse ][ - ]
| Purpose | This is a single-center, randomized, 2-period, 2-sequence, cross-over study. |
|---|---|
| Condition | Drug Interaction Potentiation |
| Intervention | Drug: Rosuvastatin, Pantoprazole |
| Phase | Phase 1 |
| Sponsor | Centre hospitalier de l'Université de Montréal (CHUM) |
| Responsible Party | Centre hospitalier de l'Université de Montréal (CHUM) |
| ClinicalTrials.gov Identifier | NCT01146483 |
| First Received | May 25, 2010 |
| Last Updated | December 14, 2011 |
| Last verified | December 2011 |
Tracking Information[ + expand ][ + ]
| First Received Date | May 25, 2010 |
|---|---|
| Last Updated Date | December 14, 2011 |
| Start Date | April 2010 |
| Estimated Primary Completion Date | December 2011 |
| Current Primary Outcome Measures | To determine changes induced by pantoprazole administration on the pharmacokinetics of rosuvastatin in healthy volunteers. [Time Frame: 2 weeks] [Designated as safety issue: No]Rosuvastatin will be administered with and without pantoprazole. |
| Current Secondary Outcome Measures | Not Provided |
Descriptive Information[ + expand ][ + ]
| Brief Title | Drug-drug Interaction Study in Healthy Male Volunteers Following the Administration of Pantoprazole and Rosuvastatin |
|---|---|
| Official Title | Drug-drug Interaction Study in Healthy Male Volunteers Following the Administration of Pantoprazole and Rosuvastatin |
| Brief Summary | This is a single-center, randomized, 2-period, 2-sequence, cross-over study. |
| Detailed Description | Background: Notions used to describe drug disposition are being reviewed as the roles of drug membrane transporters are being discovered. In the near past, simple biophysical principles - lipophilicity and passive diffusion - were used to explain drug absorption, distribution and elimination. Today, with more than 367 genes known in humans, membrane transporters occupy a much central role. Rational: Drug influx/efflux transporters are expressed in various organs with variable activities and their presence increases (influx) or decreases (efflux) the intracellular concentration of a drug in a specific organ. Therefore, intersubject variability in the activity of these transporters due to genetic polymorphisms or concomitant drug treatments can explain intersubject variability in drug actions. Rosuvastatin is an HMG-CoA reductase inhibitor and a substrate of OATPs and BCRP. There is not much information on the transporter-mediated disposition of rosuvastatin. Literature suggests that rosuvastatin is a transporter substrate of the influx OATP1B1, 1B3 and 2B1 as well as the efflux BCRP. The efflux of rosuvastatin by BCRP would be of major importance in the hepatocytes. BCRP would be responsible of the excretion of 30% of the unchanged drug in the bile. To confirm this hypothesis and identify patients at risk of toxicity with rosuvastatin, we want to perform a drug-drug interactions study with an inhibitor of BCRP namely, pantoprazole. With this approach, we will confirm if rosuvastatin is a real substrate of BCRP as suggested in the literature. Methodology: To determine changes induced by the administration of pantoprazole on the pharmacokinetics of rosuvastatin in healthy volunteers 16 healthy volunteers will be administered a single dose of rosuvastatin with and without (placebo) pantoprazole. Urine and plasma analysis will be performed by LC-MSMS. Pharmacokinetics analysis will be performed. Plasma and urine concentrations of rosuvastatin will be analysed using a noncompartmental method. Pharmacokinetic parameters calculated in this study will be Cmax, Tmax, AUC0-72, AUC0-∞, Kel, T1/2β, CL/F, CLr, and Ae. |
| Study Type | Interventional |
| Study Phase | Phase 1 |
| Study Design | Allocation: Randomized, Endpoint Classification: Pharmacokinetics Study, Intervention Model: Crossover Assignment, Masking: Single Blind (Subject), Primary Purpose: Basic Science |
| Condition | Drug Interaction Potentiation |
| Intervention | Drug: Rosuvastatin, Pantoprazole Rosuvastatin, 10 mg tablets, single dose on the morning Concomitant drug: Pantoprazole; 40 mg tablets, 2 single doses administered 1 hour before rosuvastatin and 23 hours after rosuvastatin administration. A placebo is given on the other period as a crossover design study. Other Names:
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Recruitment Information[ + expand ][ + ]
| Recruitment Status | Completed |
|---|---|
| Estimated Enrollment | 16 |
| Estimated Completion Date | December 2011 |
| Estimated Primary Completion Date | December 2011 |
| Eligibility Criteria | Inclusion Criteria: - Vital Signs, EKG and Clinical Laboratory Values within the normal range - Body mass index (BMI) [20-29kg/m2] - Caucasian male - Age between [18-55] - Healthy by physical exam - Non or ex-smoker Exclusion Criteria: - Presence or history of intolerance or hypersensibility to proton pump inhibitors or HMG-CoA reductase inhibitors. - Significant illness. History of cardiovascular, kidney, liver or gastrointestinal disease. Presence of cardiovascular, pulmonary, hematologic, neurologic, psychiatric, endocrine, immunologic or dermatologic disease. - consumption of an investigational product or donation of blood in the previous 28 days preceding the study. |
| Gender | Male |
| Ages | 18 Years |
| Accepts Healthy Volunteers | Accepts Healthy Volunteers |
| Contacts | Not Provided |
| Location Countries | Canada |
Administrative Information[ + expand ][ + ]
| NCT Number | NCT01146483 |
|---|---|
| Other Study ID Numbers | CE 09.252 |
| Has Data Monitoring Committee | No |
| Information Provided By | Centre hospitalier de l'Université de Montréal (CHUM) |
| Study Sponsor | Centre hospitalier de l'Université de Montréal (CHUM) |
| Collaborators | Centre de Recherche du Centre Hospitalier de l'Université de Montréal |
| Investigators | Principal Investigator: Pavel Hamet, M.D., Ph.D. Centre hospitalier de l'Université de Montréal (CHUM) |
| Verification Date | December 2011 |
Locations[ + expand ][ + ]
| Centre hospitalier de l'Université de Montréal (CHUM) | Montreal, Quebec, Canada, H2W1T7 |
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