A Study to Evaluate Pharmacokinetic/Pharmacodynamic Drug-drug Interaction and Safety/Tolerability Between RLD2202 and RLD2203
NCT ID: NCT05481307
Last Updated: 2023-09-22
Study Results
The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.
Basic Information
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COMPLETED
PHASE1
24 participants
INTERVENTIONAL
2022-08-02
2022-10-25
Brief Summary
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Detailed Description
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Conditions
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Study Design
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NA
SEQUENTIAL
TREATMENT
NONE
Study Groups
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Fixed Sequence
Period 1: RLD2202, Period 2 : RLD2203 -\> RLD2202+RLD2203
RLD2202
Take it once a day per period
RLD2203
Take it once a day per period
Interventions
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RLD2202
Take it once a day per period
RLD2203
Take it once a day per period
Eligibility Criteria
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Inclusion Criteria
2. Body mass index (BMI) in the range of 18 to 27 kg/m2 and weight 50kg to 90kg.
3. After fully hearing and understanding the details of this clinical trial, Subjects who have willingness to sign of informed consent before the screening.
4. Subject who are eligible from physical examination, clinical laboratory test by investigators judgment.
Exclusion Criteria
2. Subjects who judged ineligible by the investigator
19 Years
50 Years
ALL
Yes
Sponsors
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Hanmi Pharmaceutical Company Limited
INDUSTRY
Responsible Party
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Principal Investigators
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SeungHwan Lee, M.D.
Role: PRINCIPAL_INVESTIGATOR
Seoul National University Hospital
Locations
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Seoul National University Hospital
Seoul, , South Korea
Countries
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Other Identifiers
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HM-SARA-101
Identifier Type: -
Identifier Source: org_study_id
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