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Completed Phase 2 Interventional Results available

An Efficacy, Safety, Tolerability and Dose Finding Study of XXB750 in Resistant Hypertension Patients.

ClinicalTrials.gov ID: NCT05562934

Public ClinicalTrials.gov record NCT05562934. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 29, 2026, 12:18 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Multi-center, Randomized, Double-blind, Parallel-group, 20-week Dose-finding Study to Evaluate Efficacy, Safety, and Tolerability of XXB750 in Patients With Resistant Hypertension

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The purpose of this 20-week randomized double-blind study in patients with resistant hypertension (rHTN) is to evaluate the efficacy, safety, and tolerability, of different doses of XXB750 administered as subcutaneous (SC) injections, compared to placebo. Since all study participants will be patients with rHTN, all study treatments will be given on top of maximally tolerated background antihypertensive therapy recommended by international guidelines for treatment of HTN (i.e., a thiazide or a thiazide-like diuretic, an angiotensin converting enzyme inhibitor (ACEi) or an angiotensin receptor blocker (ARB), and a long-acting dihydropyridine calcium channel blocker (CCB).

Study identification

NCT ID
NCT05562934
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Novartis Pharmaceuticals
Industry
Enrollment
189 participants

Conditions and interventions

Interventions

Biological · Other

Eligibility (public fields only)

Age range
18 Years to 100 Years
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Nov 8, 2022 (Actual)
Primary completion
Jul 2, 2024 (Actual)
Completion
Aug 27, 2024 (Actual)
Last update posted
Jan 12, 2026

2022 – 2024

United States locations

U.S. sites
18
U.S. states
10
U.S. cities
18
Facility City State ZIP Site status
Pinnacle Research Group Llc Anniston Alabama 36207 —
Parkway Medical Center Birmingham Alabama 35206 —
Clinical Trials Research Sacramento Sacramento California 95821-2134 —
Orange County Research Center Tustin California 92780 —
Jacksonville Center for Clinical Research Jacksonville Florida 32216 —
Canvas Clinical Research Lake Worth Florida 33467 —
Inpatient Research Clinical LLC Miami Lakes Florida 33014 —
Cardiology Partners Clinical Research Institute Wellington Florida 33449 —
American Clinical Trials Acworth Georgia 30101 —
Alliance for Multispecialty Resrch Wichita Kansas 67207 —
Anderson Medical Research Ft. Washington Maryland 20744 —
Capitol Cardiology Associates Lanham Maryland 20706 —
MD Medical Research Oxon Hill Maryland 20745 —
NexGen Research Lima Ohio 45801 —
The Research Center of the Upstate Greenville South Carolina 29607 —
Tennessee Center For Clinical Trials Tullahoma Tennessee 37388 —
Manassas Clinical Research Center Manassas Virginia 20110 —
Dominion Medical Associates Richmond Virginia 23219 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 60 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05562934, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jan 12, 2026 · Synced Oct 29, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05562934 live on ClinicalTrials.gov.

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