CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 27 enrolled
Drug / intervention
AZD3355 +4 moredrug
Likely dose
AZD3355 30 mgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT01043185
NCT01043185Phase 2Completed

A Double-blind, Placebo Controlled, Randomised, Phase IIA Pharmacodynamic 4-way Cross-over Study to Estimate the Dose Response Relationship of AZD3355 on the Number of Reflux Episodes Assessed by Impedance/pH in Patients With GERD and a Partial Response to PPI Treatment

AstraZeneca·interventional·Posted Jan 6, 2010·Updated Jun 14, 2011

In Brief

A Phase 2 clinical trial evaluating AZD3355 and placebo for Gastroesophageal Reflux Disease. Completed, enrolled 27 participants across 1 site.

Detailed Summary

The purpose of the study is to estimate what effect 4 different doses of AZD3355 will have on the number of reflux episodes, in patients who have GERD and still experience symptoms despite proton pump inhibitor (PPI) treatment.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesUnited States
Collaborators--

Timeline

Phase 2CompletedFinished
20102011201220132014201520162017201820192020202120222023202420252026
First PostedJan 6, 2010
Enrollment StartDec 1, 2009
Primary CompletionMay 1, 2010
TodayJul 2, 2026
Enrollment to primary: 5 monthsPosted 16.5 years ago

Interventions

AZD3355drug

30 mg orally in the morning and 30 mg in the evening for 1 day

AZD3355drug

90 mg orally in the morning and 90 mg in the evening for 1 day

AZD3355drug

120 mg orally in the morning and 120 mg in the evening for 1 day

AZD3355drug

240 mg orally in the morning and 240 mg in the evening for 1 day

placebodrug

Placebo capsules orally in the morning and placebo capsules in the evening for 1 day