Status:
COMPLETED
A Study to Evaluate the Drug-drug Interaction and Safety Between "BR6001-1" and "BR6001-2"
Lead Sponsor:
Boryung Pharmaceutical Co., Ltd
Conditions:
Gastric or Duodenal Ulcer
Eligibility:
All Genders
19-55 years
Phase:
PHASE1
Brief Summary
The purpose of this clinical trial is to evaluate the drug-drug interaction and safety between "BR6001-1" and "BR6001-2" in healthy adult volunteers
Eligibility Criteria
Inclusion
- Those who weigh 50 kg or more and have body mass index (BMI) within the range of 18.0 to 30.0kg/m² at screening visit.
- Those who sign written consent spontaneously to follow the study directions after listening to and understanding sufficient explanation of this clinical trial.
Exclusion
- Those who have a medical history of gastrointestinal diseases(Crohn's disease, ulcer, acute or chronic pancreatitis, etc.) or gastrointestinal surgery (Except for simple appendectomy, hernia surgery) that may affect the absorption of investigational products.
- Those who have hypersensitivity reaction to investigational products or their additives in addition to other painkillers, anti-inflammatory drugs, antirheumatic drugs, benzimidazole.
- Those who have a history of clinically significant hypersensitivity reaction.
- Those taking anticoagulants, atazanavir, Rilpivirine and methotrexate.
- Those who eat an abnormal food that may affect the absorption, distribution, metabolism and excretion of investigational products or who eat food that may affect drug metabolism.
- Those who take any prescription drugs(including herbal medicines) that may affect characteristics of investigational product within 14 days prior to the date of first administration or who take any over-the-counter (OTC) drugs or vitamins within 10 days prior to the date of first administration (however, if it don't affect subject's safety and study's result according to the judgment of the investigator, they may participate in the study.)
- Those who take inducer and inhibitor of drug metabolizing enzymes such as barbiturates, etc. within 1 month prior to the first administration
Key Trial Info
Start Date :
March 30 2023
Trial Type :
INTERVENTIONAL
Allocation :
ACTUAL
End Date :
May 9 2023
Estimated Enrollment :
30 Patients enrolled
Trial Details
Trial ID
NCT06165237
Start Date
March 30 2023
End Date
May 9 2023
Last Update
February 1 2024
Active Locations (1)
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1
ChungBuk National University Hospital
Jungbuk, South Korea