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| Sponsor: | AstraZeneca |
|---|---|
| Information provided by: | AstraZeneca |
| ClinicalTrials.gov Identifier: | NCT00684190 |
Purpose
The purpose of the study is to evaluate if AZD3355 and Nexium interact with each other or not, i.e. show the same or altered plasma concentration profiles when co-administered compared to administered alone.
| Condition | Intervention | Phase |
|---|---|---|
|
Gastroesophageal Reflux Disease |
Drug: AZD3355 Drug: Esomeprazole |
Phase I |
| Study Type: | Interventional |
| Study Design: | Allocation: Randomized Endpoint Classification: Pharmacokinetics Study Intervention Model: Crossover Assignment Masking: Open Label Primary Purpose: Basic Science |
| Official Title: | An Open, Randomised, Three Period Cross, Single Centre, Phase 1 Pharmacokinetic Interaction Study of the Reflux Inhibitor AZD3355 150 mg Bid and Esomeprazole 40 mg od After 7 Days of Treatment in Healthy Volunteers |
| Enrollment: | 30 |
| Study Start Date: | March 2008 |
| Study Completion Date: | June 2008 |
| Primary Completion Date: | June 2008 (Final data collection date for primary outcome measure) |
| Arms | Assigned Interventions |
|---|---|
|
Experimental: 1
AZD3355 150 mg
|
Drug: AZD3355
150 mg bid, oral, 7 days
Other Name: Lesogaberan
|
|
Experimental: 2
Esomeprazole 40mg
|
Drug: Esomeprazole
40 mg od, oral, 7 days
Other Name: Nexium
|
|
Experimental: 3
AZD3355 150mg/Esomeprazole 40mg
|
Drug: AZD3355
150 mg bid, oral, 7 days
Other Name: Lesogaberan
Drug: Esomeprazole
40 mg od, oral, 7 days
Other Name: Nexium
|
Eligibility| Ages Eligible for Study: | 18 Years to 45 Years |
| Genders Eligible for Study: | Both |
| Accepts Healthy Volunteers: | Yes |
Inclusion Criteria:
Exclusion Criteria:
Contacts and Locations| Sweden | |
| Research Site | |
| Uppsala, Sweden | |
| Study Director: | Eva Ersdal, PhD | AstraZeneca R&D, Mölndal, Sweden |
| Principal Investigator: | Jan Vouis, MD | Quintiles AB, Uppsala, Sweden |
More Information
| Responsible Party: | Debra G. Silberg, MD, PhD, Medical Science Director, AZD3355, AstraZeneca Pharmaceuticals |
| ClinicalTrials.gov Identifier: | NCT00684190 History of Changes |
| Other Study ID Numbers: | D9120C00016, EudraCt nr 2007-007128-16 |
| Study First Received: | May 22, 2008 |
| Last Updated: | December 2, 2010 |
| Health Authority: | Sweden: Medical Products Agency |
|
Reflux Inhibitor GERD PPI Interaction |
|
Gastroesophageal Reflux Esophageal Motility Disorders Deglutition Disorders Esophageal Diseases Gastrointestinal Diseases Digestive System Diseases Omeprazole |
Anti-Ulcer Agents Gastrointestinal Agents Therapeutic Uses Pharmacologic Actions Enzyme Inhibitors Molecular Mechanisms of Pharmacological Action |