New shot aims to keep blood pressure in check after hospital discharge
NCT ID NCT07511361
First seen Jun 25, 2026 · Last updated Sep 03, 2026 · Updated 5 times
Summary
This study tests a drug called tonlamarsen in adults who were recently hospitalized for dangerously high blood pressure. Participants receive either the drug or a placebo as a shot under the skin every 4 weeks. The goal is to see if tonlamarsen can lower blood pressure and reduce a protein linked to hypertension, helping patients stay healthy after leaving the hospital.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- tonlamarsen
- What this could lead to
- If it works, this could provide a new treatment option to help control blood pressure after a severe hypertensive episode, potentially reducing the risk of future hospitalizations.
- What could go wrong
- This is an early Phase 2b trial with only 100 participants, so results may not apply to everyone. The drug may not lower blood pressure significantly or could have side effects.
Why investors are watching
Kardigan is a micro-cap company, so a single late-stage trial can define its value. This phase 2b study tests whether tonlamarsen lowers blood pressure in 140 adults who recently left the hospital after a severe hypertension episode. A clear result would tell investors whether the drug works in a high-risk patient group, which matters more for a small company than for a large one.
If it works: A positive result could position tonlamarsen as a viable treatment for acute severe hypertension, giving Kardigan a lead asset to advance toward later trials. That outcome might attract partnership interest or funding to support further development.
If it fails: The trial could fail to show a meaningful blood pressure reduction, or safety issues could emerge, which would likely end the drug's development. Trials at this stage often fail, and for a micro-cap company, a negative readout could leave Kardigan without a clear path forward.
AI-written from the trial record. Speculative, and not investment advice.
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
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Phase 2
Tests whether the treatment actually works, and watches for side effects, in a larger group.
- Participants
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About 140 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Jun 2026
- Expected to finish
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Feb 2027
An estimate. End dates often move.
- Lead sponsor
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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
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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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.
Key Inclusion Criteria: * Age 18 or older, body weight ≥ 50 kg with BMI ≤45.0 kg/m2 * Ready for discharge or recently discharged from the hospital to home (within the past 7 days) during which evaluation and/or treatment of acute severe hypertension (documented SBP ≥ 180 mmHg and/or DBP ≥ 110 mmHg) occurred, as measured by a healthcare provider (HCP) within the 24 hours preceding hospitalization or during the initial 24 hours of hospitalization * At Screening and Randomization visit, average resting office systolic blood pressure ≥ 145 mmHg * Presence of established cardiovascular or renal disease Key Exclusion Criteria: * Has known history of secondary hypertension * Any malignancy requiring treatment within 5 years (except for basal or squamous cell carcinoma of the skin or carcinoma in situ of the cervix that has been successfully treated) * Has abnormal thyroid function with clinical significance * Recent hospitalization for stroke, myocardial infarction or coronary revascularization within 30 days prior to screening * History of and/or obvious clinical signs or symptoms of cirrhosis or other significant liver disease * Alanine aminotransferase or aspartate aminotransferase \>2 x upper limit of normal * Most recent hospitalization was for non-cardiovascular or non-renal conditions
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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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
11 sites. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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Baylor Scott and White Research Institute - Temple
RECRUITINGTemple, Texas, 76502, United States
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Chattanooga Research & Medicine CHARM
RECRUITINGChattanooga, Tennessee, 37404, United States
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Eagle Clinical Research
RECRUITINGChicago, Illinois, 60621, United States
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Homestead Associates in Research
RECRUITINGHomestead, Florida, 33033, United States
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Laguna Clinical Research Associates
RECRUITINGLaredo, Texas, 78041, United States
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OnSite Clinical Solutions, LLC
RECRUITINGFort Mill, South Carolina, 29715, United States
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Progressive Medical Research
RECRUITINGPort Orange, Florida, 32127, United States
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Research Innovations, LLC
RECRUITINGBeavercreek, Ohio, 05431, United States
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Richmond University Medical Center (RUMC)
RECRUITINGStaten Island, New York, 10310, United States
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Tapia Internal Medicine Clinic
RECRUITINGParis, Texas, 75460, United States
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Western Nephrology and Metabolic Bone Disease, PC - Arvada
RECRUITINGArvada, Colorado, 80002, United States
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