Korea University Ansan Hospital
Seoul, South Korea
NCT Number: NCT03967886
Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients
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Notify Me20 year–70 year
All sexes
Interventional
Phase 3
Seoul, South Korea
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).
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
** Symptom (heartburn and acid regurgitation) is confirmed by RDQ
Exclusion criteria
Patients should take drugs an hour before breakfast.
Patients should take drugs an hour before breakfast.
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.
Time frame: within 4 weeks
Recovered percentage(%) of the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline).
Time frame: within 4 weeks
Change of the score about the symptom(heartburn or/and acid regurgitation) measured by RDQ after administration(baseline).
Time frame: within 4 weeks
Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the daytime measured by Patients diary after administration(baseline).
Time frame: within 4 weeks
Percentage(%) of the patients who have symptom(heartburn or/and acid regurgitation) during the nighttime measured by Patients diary after administration(baseline).
Time frame: within 4 weeks
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).
Yooyoung Pharmaceutical Co., Ltd.
Industry
A Randomized, Double-blind, Placebo-controlled, Multi-centers Clinical Trial to Assess the Efficacy and Safety of YYD601 in NERD Patients (Phase3).
OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.
View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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