New combo diabetes pill passes early safety check in healthy people
NCT ID NCT07128654
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This early-stage study tested a new combination pill (CTL02) that contains two diabetes drugs (alogliptin and empagliflozin) in a single tablet. Forty healthy adults received either the combo pill or the two drugs separately to compare safety and how the body processes them. The trial is complete and focused on basic safety and drug levels, not on treating any disease.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- CTL02 (a fixed-dose combination tablet of alogliptin and empagliflozin)
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
-
40 people
The number who actually took part.
- Started
-
Sep 2025
- Finished
-
Oct 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 55 days
- Sex
-
Anyone
- Healthy volunteers
-
Accepted
You do not need to have the condition being studied to take part.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: * Healthy participant aged 19 to 55 years, at screening * A participant who has a body mass index (BMI) of 18.0\~29.9 kg/m2, at screening * A participant who is judged to be eligible to participate by the results of screening tests (vital signs, clinical laboratory tests, 12-lead ECG, etc.) by the principal investigator Exclusion Criteria: * A participant who has taken drugs that induce or inhibit drug metabolizing enzymes * A participant who has participated in other clinical trials or bioequivalence studies within 6 months prior to the first dose of the investigational drug * A participant who has a history of gastrointestinal surgery that may affect drug absorption
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
H+ Yangji Hospital
Seoul, South Korea
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