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Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients
This Phase 3 Clinical Trial is Designed as Randomized, Double-blind, Placebo-controlled, Multi-centers Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients (Phase3).
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| Label | Type | Description | Intervention Names |
|---|---|---|---|
| YYD601 20mg | Experimental | Esomeprazole magnesium Dihydrate. |
|
| Nexium 20mg | Active Comparator | Esomeprazole magnesium trihydrate, a substituted benzimidazole. |
|
| Name | Type | Description | Arm Group Labels | Other Names |
|---|---|---|---|---|
| YYD601 20mg | Drug | Patients should take drugs an hour before breakfast. |
| |
| Measure | Description | Time Frame |
|---|---|---|
| Recovered percentage(%) of the symptom | Recovered percentage(%) of the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline). | within 4 weeks |
| Change of the score about the symptom | Change of the score about the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline). | within 4 weeks |
| Percentage(%) of the patients who have symptom during the daytime | Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the daytime measured by Patients diary after administration(baseline). | within 4 weeks |
| Percentage(%) of the patients who have symptom during the nighttime | Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the nighttime measured by Patients diary after administration(baseline). | within 4 weeks |
| Percentage(%) of the days no symtom | Percentage(%) of the days no symptom(heartburn or/and acid regurgitation) among the patients who have symptom(heartburn or/and acid regurgitation) during the nighttime measured by Patients diary after administration(baseline). | within 4 weeks |
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Inclusion Criteria:
A man or woman over 20 years old less than 70 years old.
A man or woman who has below all characters and diagnosis as NERD.
A man or woman who has experienced symptom(hearburn or/and acid regurgitation) over 3month at least.
A man or woman who has experienced symptom(heartburn or/and acid regurgitation) within 7days before Visit1, meet below 1) or 2) criteria.
** Symptom (heartburn and acid regurgitation) is confirmed by RDQ
A man or woman who has been made diagnosis as LA grade0(Zero) measured through the dendoscopy which is corried out within 14 days, there is no observed muscosal break.
A man or woman who has a full understanding of this clinical trial through the detailed explanation, agree in writing to participate in this trial.
Exclusion Criteria:
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| Facility | Status | City | State | ZIP | Country | Contacts |
|---|---|---|---|---|---|---|
| Korea University Ansan Hospital | Seoul | South Korea |
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| ID | Term |
|---|---|
| D000096663 | Non-Erosive Reflux Disease |
| ID | Term |
|---|---|
| D005764 | Gastroesophageal Reflux |
| D015154 | Esophageal Motility Disorders |
| D003680 | Deglutition Disorders |
| D004935 | Esophageal Diseases |
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| ID | Term |
|---|---|
| D064098 | Esomeprazole |
| ID | Term |
|---|---|
| D009853 | Omeprazole |
| D053799 | 2-Pyridinylmethylsulfinylbenzimidazoles |
| D013454 | Sulfoxides |
| D013457 | Sulfur Compounds |
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| Nexium 20mg |
| Drug |
Patients should take drugs an hour before breakfast. |
|
| Placebos | Drug | The placebo YYD601 is made from microcrystalline cellulose covered with hard shell. The placebo Nexium is made from microcrystalline cellulose, Crospovidone, Magnesiumstearat and other ingredients. |
|
| D005767 | Gastrointestinal Diseases |
| D004066 | Digestive System Diseases |
| D009930 |
| Organic Chemicals |
| D011725 | Pyridines |
| D006573 | Heterocyclic Compounds, 1-Ring |
| D006571 | Heterocyclic Compounds |
| D001562 | Benzimidazoles |
| D006574 | Heterocyclic Compounds, 2-Ring |
| D000072471 | Heterocyclic Compounds, Fused-Ring |