See if ARNi therapy helps people with high blood pressure in the UAE
Official title: Real-world Effectiveness of Angiotensin Receptor-Neprilysin Inhibitor (ARNi) Therapy in Lowering Blood Pressure in Hypertensive Patients in the United Arab Emirates
Run by Novartis · NCT07465666 · Data updated 2026-11-12
This real-world study tests whether sacubitril/valsartan (ARNi) or single-drug blood pressure medicine can lower blood pressure in adults with hypertension in the United Arab Emirates.
Quick facts
| Study type | Observational |
|---|---|
| Ages | 18 Years to 99 Years |
| Sex | All |
| Enrollment | 500 (estimated) |
| Sponsor | Novartis Industry-sponsored |
| Locations | 4 sites (Abu Dhabi and 3 other locations) |
| Status | Recruiting |
| Started | October 15, 2026 |
| Main results expected | August 31, 2027 |
| Study ends | August 31, 2027 |
| Registry record updated | October 21, 2026 |
| Trial ID | NCT07465666 on ClinicalTrials.gov |
Is this trial a fit for you?
✓Likely a good fit
Adults (≥18) with physician-diagnosed hypertension in the UAE who are either antihypertensive therapy naïve or on monotherapy and transitioning to ARNi.
✕Probably not a fit
Patients who do not respond to ARNi or who do not undergo the mandated transition may not see a BP benefit.
A plain-English reading of the study's rules. Only the study team can confirm whether you qualify.
What this trial studies
This observational study will look at how well ARNi therapy, compared with antihypertensive monotherapy such as ACE inhibitors, ARBs, or calcium channel blockers, lowers blood pressure in adults with hypertension. It uses real-world clinical practice data to assess effectiveness after initiating ARNi or transitioning from monotherapy to ARNi. The study focuses on patients residing in the UAE and follows standard care without randomization or experimental interventions. Eligibility includes adults with diagnosed hypertension and elevated office blood pressure, with requirements around treatment transition and consent. Exclusion criteria omit patients with severely high blood pressure at baseline and certain other conditions as defined by protocol.
Why it matters
Potential benefit: If successful, the study could support ARNi therapy as a real-world option for achieving better blood pressure control in UAE patients.
How similar studies have gone: Other real-world studies have explored ARNi use in hypertension, but this specific UAE-based observational approach is relatively novel.
Who can join: the full rules
Show full inclusion / exclusion criteria
Inclusion criteria: 1. Adult male or female patients (≥18 years). 2. Patients with physician-diagnosed hypertension (as defined by international guidelines including the American Heart Association/American College of Cardiology \[AHA/ACC\] guidelines and/or the 2024 European Society of Cardiology \[ESC\] guidelines). 3. Patients with documented office blood pressure ≥130/80 mmHg prior to initiating treatment (ARNi or monotherapy) or transitioning from monotherapy to ARNi. 4. Patients who are either antihypertensive therapy naïve or currently receiving antihypertensive monotherapy (ACE inhibitor/ARB/CCB) with a physician-directed requirement to transition to ARNi. Note: Patients who transition from one monotherapy to another during the study are not eligible for inclusion. 5. Patients willing to provide written informed consent to participate in the study. Exclusion criteria: 1. Patients with malignant or severe hypertension (systolic blood pressure \[SBP\] ≥180 mmHg, diastolic blood pressure \[DBP\] ≥110 mmHg) at baseline. 2. Patients with secondary causes of hypertension, as determined by the treating physician. 3. Patients with a history of, or at risk of developing, angioedema. 4. Patients with evidence of severe renal impairment (e.g., estimated glomerular filtration rate \[eGFR\] \<30 mL/min/1.73 m\^2). 5. Pregnant or lactating women. 6. Patients with serum potassium level ≥5.5 mmol/L at baseline.
Where it's running
-
Novartis Investigative Site
Abu Dhabi, United Arab Emirates Recruiting -
Novartis Investigative Site
Dubai, United Arab Emirates Recruiting -
Novartis Investigative Site
Fujairah, United Arab Emirates Recruiting -
Novartis Investigative Site
Ras al-Khaimah, United Arab Emirates Recruiting
Study contacts
- Study coordinator: Novartis Pharmaceuticals
- Email: novartis.email@novartis.com
- Phone: +41613241111
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How to take part
- Review the eligibility criteria above with your treating physician.
- Check the official listing on ClinicalTrials.gov for the latest contact details and recruitment status.
- Contact the study coordinator or principal investigator to ask for pre-screening. Pre-screening is free and never obligates you to enroll.