NCT07142356RecruitingPhase 2
A Study of Modified Release RTN-001 In Patients With Uncontrolled Hypertension
A Randomized, Double-Blind, Placebo Controlled, Parallel Group, Multicenter Study of Modified Release RTN-001 In Patients With Uncontrolled Hypertension
Source: ClinicalTrials.gov · Last updated 4 Nov 2026
Brief summary (registry, in English)
The purpose of this clinical trial is to measure the safety and efficacy of RTN-001 in adult participants with uncontrolled hypertension versus placebo.
- Status (registry)
- Recruiting
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 280 (estimated)
- First submitted
- 19 Aug 2025
- Start date
- 31 Oct 2025
- Primary completion date
- Mar 2027
- Lead sponsor
- Retension Pharmaceuticals. Inc.
- Diseases
- High blood pressure
- NCT number
- NCT07142356
What you commit to
- Study type: Interventional · Phase 2
- Planned participants: 280
- From 31 Oct 2025 to the primary completion date, Mar 2027
- 42 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Current or planned use of nitrates and/or alpha-blockers or other drugs known to affect BP during the study period.
- Participants who use PDE5 inhibitors for other indications that cannot or will not refrain from use of PDE5 inhibitors for 7 days before and during their entire period of participation in the study.
- Recent (within 3 months before the Screening Visit \[Visit S1\]) myocardial infarction; unstable angina leading to hospitalization; uncontrolled, symptomatic atrial fibrillation, or any cardiac arrhythmia that has not been clinically stable for at least 3 months prior to screening. Participants with implantable pacemakers or automatic implantable cardioverter defibrillators may be considered if deemed by the Investigator to be stable for the previous 3 months.
- Any prescription or over-the counter drugs or herbal supplements known to be strong inhibitors of CYP3A4 enzymes
Other illness
- History of hypotension, fainting spells, blackouts or autonomic dysfunction, including orthostatic hypotension.
- Known diagnosis of secondary hypertension (e.g. Cushing's Disease or hyperaldosteronism, renal fibrodysplasia, renal artery stenosis, etc., clinically significant aortic stenosis etc.).
- Liver disease or dysfunction
- Active infection or major illness
- Gastrointestinal conditions or procedures (including weight loss surgery \[eg, Lap-Band or gastric bypass\]) that may affect drug absorption.
- Hematologic or coagulation disorders
- Active malignancy
- A known history of temporary or permanent partial or total vision loss
- A known history of "crowded" optic disc.
- A known history of retinitis pigmentosa, a rare genetic eye disease.
- NHYA class III-IV symptoms of heart failure.
Lab values
- Unexplained creatine kinase (CK) \>3 × ULN at any time before randomization
- History of diabetes or suspected diabetes with glycosylated hemoglobin \> 10% or fasting glucose \>250 mg/dl at Screening Visit (S1).
Other
- Mean seated SBP \>175 mm Hg and/or DBP \>110 mm Hg.
- Uncontrolled hypothyroidism
- Renal dysfunction (\<45 mL/min/1.73m²) or glomerulonephritis
Who the study is looking for
- Male or female patients age 18 to 75 years, inclusive, at the Screening Visit.
- Uncontrolled HTN despite being on a stable regimen of 2-5 antihypertensive medications.
- Mean BP of ≥135/80 mm Hg.
- Body mass index of 18 to 35 kg/m2.
Age in the registry: 18 years to 75 years · Sex: All · Does not accept healthy volunteers
Sites (42)
Sites in registry order. Pick your city on the disease page to sort them by distance.
This page is information, not medical advice. Discuss any trial with your doctor.