New drug candidate AGSAVI aims to lower stubborn high blood pressure
NCT ID NCT05503953
First seen Jun 27, 2026 · Last updated Sep 11, 2026 · Updated 2 times
Summary
This phase 3 study tests whether the drug AGSAVI can lower blood pressure in people with essential hypertension that is not well controlled by the drug AGLS. About 318 adults with high blood pressure will receive either AGSAVI or AGLS, and their sitting blood pressure will be measured over 10 weeks. The goal is to see if AGSAVI provides better blood pressure control.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- AGSAVI
- What this could lead to
- If successful, AGSAVI could offer a new treatment option for people with high blood pressure that is not well controlled by current medications.
- What could go wrong
- This is a phase 3 trial, but results may not confirm superiority or safety over existing treatments. Side effects are possible, and individual responses may vary.
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 3
Large-scale testing in a bigger group. Usually the last step before a treatment can be approved.
- Participants
-
318 people
The number who actually took part.
- Started
-
Sep 2022
- Finished
-
Jun 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 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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: * Hypertension patient who satisfied below condition at Visit 1. * patient who takes antihypertensive drug * 140mmHg \<= MSSBP \< 200mmHg * 130mmHg \<= MSSBP \< 200mmHg at or before visit 1(In high-risk patients) * patient who doesn't take antihypertensive drug * 160mmHg \<= MSSBP \< 200mmHg * Hypertension patient who satisfied below condition at Visit 2. * 140mmHg \<= MSSBP \< 200mmHg at Visit 2 * 130mmHg \<= MSSBP \< 200mmHg at or before Visit 1(In high-risk patients) Exclusion Criteria: * Patient who have received 4 or more antihypertensive drug * Patient with 20mmHg\>= of difference in MSSBP or 10mmHg\>= of difference in MSDBP BP measuring at Visit 1 * Patient with MSDBP \>= 120mmHg at Visit 1 and 2 * Patient with secondary hypertension(including past medical history)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
-
AhnGook
Seoul, South Korea
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