NCT05432167CompletedPhase 2
A Study to Evaluate CIN-107 for the Treatment of Patients With Uncontrolled Hypertension and Chronic Kidney Disease
A Randomized, Double-Blind, Placebo-Controlled, Multicenter, Parallel-Group, Dose-Ranging Study to Evaluate CIN-107 for the Treatment of Patients With Uncontrolled Hypertension and Chronic Kidney Disease
Source: ClinicalTrials.gov · Last updated 20 May 2025
Brief summary (registry, in English)
This study will evaluate the efficacy and safety of CIN-107 for the treatment of hypertension in patients with uncontrolled hypertension (uHTN) and Chronic Kidney Disease (CKD).
- Status (registry)
- Completed
- Phase (registry)
- Phase 2
- Study type
- Interventional
- Enrollment
- 195 (actual)
- First submitted
- 20 Jun 2022
- Start date
- 29 Apr 2022
- Primary completion date
- 2 May 2024
- Lead sponsor
- AstraZeneca
- NCT number
- NCT05432167
What you commit to
- Study type: Interventional · Phase 2
- Participants enrolled: 195
- From 29 Apr 2022 to the primary completion date, 2 May 2024
- 68 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
- Has had dialysis for acute kidney injury/acute renal failure within 12 weeks prior to the Screening Period or has a planned dialysis or kidney transplantation during the course of the study.
- Has had a prior solid organ transplant or cell transplant.
- Has received immunotherapy for treatment of CKD within 6 months of Screening.
- Has any clinically relevant medical or surgical conditions including unstable conditions and/or conditions requiring regular transfusion or treatment with systemic immunosuppressants, including corticosteroids.
Other illness
- Have a documented diagnosis of type 1 diabetes.
- Has known documented chronic heart failure New York Heart Association Class III or Class IV and/or hospitalization for heart failure within 6 months of Screening.
- Has had a stroke, transient ischemic attack, hypertensive encephalopathy, acute coronary syndrome, or hospitalization for heart failure within 6 months of Screening.
- Has known current severe left ventricular outflow obstruction, such as obstructive hypertrophic cardiomyopathy and/or severe aortic valvular disease.
- Has planned any major cardiac surgery during the study or had major cardiac surgery within 6 months of Screening.
- Has a known hypersensitivity to CIN-107 or drugs of the same class
- Is positive for Human immunodeficiency disease (HIV) antibody, hepatitis B surface antigen, or hepatitis C virus Ribonucleic acid (RNA).
Lab values
- Are not willing or not able to discontinue a mineralocorticoid receptor antagonist (MRA) or a potassium sparing diuretic as part of an existing antihypertensive regimen.
- Serum potassium \<3.5 mEq/L or \>5.0 mEq/L
- Serum sodium \<135 mEq/L
- Serum aspartate aminotransferase or alanine aminotransferase \>3 × upper limit of normal (ULN); or Total bilirubin \>2 × ULN, unless due to Gilbert's syndrome.
- GFR is \< 25 or \> 75 mL/min/1.73 m2
- Has uncontrolled diabetes with glycosylated hemoglobin \>10.5%.
Other
- Have a single occurrence of mean seated SBP \>180 mmHg or DBP \>110 mmHg during the Screening Period.
- Has a body mass index (BMI) \>50 kg/m\^2.
- Has documented bilateral clinically relevant renal artery stenosis of ≥70%.
- Has typical consumption of \>14 alcoholic drinks weekly.
Who the study is looking for
- Has a mean seated SBP ≥ 140 mmHg.
- Has a prior diagnosis of mild-to-severe CKD.
- Has an elevated UACR.
- Is currently taking an angiotensin-converting enzyme inhibitor (ACEi) or angiotensin receptor blocker (ARB) at the maximum tolerated daily dose.
Age in the registry: 18 years to 130 years · Sex: All · Does not accept healthy volunteers
Sites (68)
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.