Study of Efficacy and Safety of Tonlamarsen in Participants With a Recent Hospitalization and a Concurrent Episode of Acute Severe Hypertension
Kardigan, Inc. · NCT07511361
Opens the official ClinicalTrials.gov record, with the study team’s contacts. Bored Studies doesn’t enroll anyone.
Key facts
- Compensation
- Not posted. Ask the study team before screening.
- Who can join
- Ages 18+ · All sexes
- Healthy volunteers
- Not accepted (a condition is required)
- Study type
- Interventional · Phase 2
- Target enrollment
- 140
- US sites recruiting
- 12
- Study start
- June 23, 2026
- Record last updated
- October 15, 2026
Status re-checked against ClinicalTrials.gov within the last 12 hours.
What the study is about
The purpose of this study is to evaluate the blood pressure-lowering effect of tonlamarsen in adult participants who were recently hospitalized and concurrently experienced an episode of acute severe hypertension.
Being studied: Tonlamarsen; Placebo
Conditions: Hypertension; Acute Severe Hypertension; Hypertensive Emergency; Hypertensive Urgency
Eligibility criteria
Copied from the official record. The study team makes the final decision at screening.
Show full criteria
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
Recruiting US locations
Western Nephrology and Metabolic Bone Disease, PC - Arvada
Arvada, CO 80002
Site contact: Kardigan Clinical Study Information Team · +1-877-310-5135 · clinicaltrials@kardigan.bio
Homestead Associates in Research
Homestead, FL 33033
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Progressive Medical Research
Port Orange, FL 32127
Site contact: Kardigan Clinical Study Information Team · +1-877-310-5135 · clinicaltrials@kardigan.bio
Eagle Clinical Research
Chicago, IL 60621
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Henry Ford Hospital
Detroit, MI 48202
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Research Innovations, LLC
Beavercreek, OH 05431
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Cleveland Clinic
Cleveland, OH 44195
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
OnSite Clinical Solutions, LLC
Fort Mill, SC 29715
Site contact: Kardigan Clinical Study Information Team · +1-877-310-5135 · clinicaltrials@kardigan.bio
Chattanooga Research & Medicine CHARM
Chattanooga, TN 37404
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Laguna Clinical Research Associates
Laredo, TX 78041
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Tapia Internal Medicine Clinic
Paris, TX 75460
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Baylor Scott and White Research Institute - Temple
Temple, TX 76502
Site contact: Kardigan Clinical Study Information Team · 1-877-310-5135 · clinicaltrials@kardigan.bio
Study contacts (from the official record)
- Kardigan Clinical Study Information Team · +1-877-310-5135 · clinicaltrials@kardigan.bio
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