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Clinical Trial Details — Status: Not yet recruiting

Administrative data

NCT number NCT05842408
Other study ID # DA5212_FDQ_III
Secondary ID
Status Not yet recruiting
Phase Phase 3
First received
Last updated
Start date May 2023
Est. completion date December 2024

Study information

Verified date April 2023
Source Dong-A ST Co., Ltd.
Contact Seok-chae Choi, PhD
Phone 063-859-2550
Email medcsc@wku.ac.kr
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This study is to evaluate efficacy and safety of DA-5212 in patients with functional dyspepsia


Recruitment information / eligibility

Status Not yet recruiting
Enrollment 380
Est. completion date December 2024
Est. primary completion date June 2024
Accepts healthy volunteers No
Gender All
Age group 19 Years and older
Eligibility Inclusion Criteria: - Men or women = 19 years of age - Patients who diagnosed with functional dyspepsia - Patients with no organic cause for digestive symptoms found by upper gastrointestinal endoscopy at screening visit Exclusion Criteria: - Patients with organic disease or medical history that may cause dyspepsia within 6 months before screening visit - Patients who have a history of drugs or alcohol abuse and dependence within 6 months before screening visit - Patients with hypersensitivity to investigational drugs and similar drugs - Pregnant or breastfeeding women

Study Design


Related Conditions & MeSH terms


Intervention

Drug:
DA-5212
Test drug: DA-5212
DA-5212-R
Control drug: DA-5212-R

Locations

Country Name City State
Korea, Republic of Wonkwang University Hospital Iksan Muwangro 895

Sponsors (1)

Lead Sponsor Collaborator
Dong-A ST Co., Ltd.

Country where clinical trial is conducted

Korea, Republic of, 

Outcome

Type Measure Description Time frame Safety issue
Primary Change in NDI-K functional dyspepsia score Change from baseline at 4 weeks
Secondary Change in overall treatment score of patients Change from baseline at 4 weeks
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