New drug interaction study completed in 12 healthy volunteers
NCT ID NCT06846684
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tested whether a new drug called SB17170 changes how the body processes another drug, SB_MDZ. Twelve healthy adults took SB17170 by mouth and received SB_MDZ through an IV. Researchers measured drug levels in the blood to see if there is an interaction. The study is complete, but results are not yet available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- SB17170 and SB_MDZ
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
-
Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
-
12 people
The number who actually took part.
- Started
-
Mar 2025
- Finished
-
Sep 2025
- Lead sponsor
-
A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
-
19 to 50 years
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Healthy adult subjects aged 19 to 50 years at the time of written consent. 2. Individuals with a body weight of ≥ 50.0 kg, and a Body Mass Index(BMI) of ≥ 18.0 kg/m2 and \< 30.0 kg/m2 at the time of screening ☞ BMI(kg/m2) = weight(kg) / {height(m)}2 3. Individuals who have voluntarily provided written consent to participate in the trial, after being fully informed about the study and agreeing to follow all precautions associated with participation. Exclusion Criteria: 1. Individuals with a clinically significant disease or history in hepatobiliary, renal, nervous, respiratory, immune, hemato-oncology, cardiovascular, urinary system, or psychiatric disorder 2. Individuals with a history of a gastrointestinal disorders (gastrointestinal ulcers, gastritis, stomach cramps, gastroesophageal reflux disease, Crohn's disease, etc) or surgeries (except for simple appendectomy or hernia surgery) that may affect the safety and pharmacokinetic assessment of the investigational product (IP) 3. Individuals with hypersensitivity or significant history of hypersensitivity to drugs, including ingredients of the IP (SB17170 or its metabolite SB1703, SB\_MDZ, and benzodiazepine-class drugs) or other drugs (e.g., aspirin, antibiotics) 4. Individuals with a current or historical condition that may increase risk, as determined by the investigator or as indicated in SB\_MDZ's product information 5. Individuals who exhibited one or more of the following results in clinical laboratory tests during the screening, including additional tests * AST (SGOT), ALT (SGPT) \> 60 IU/L * Estimated glomerular filtration rate (eGFR, CKD-EPI equation): \< 60 mL/min/1.73m2 * Individuals with a positive result on serology tests (heapatitis B, hepatitis C, human immunodeficiency virus (HIV) and syphilis tests)
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Genom att skicka in godkänner du våra Användarvillkor
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
Seoul National University Hospital
Seoul, South Korea
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