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Active, not recruiting Phase 3

A Master Protocol Study of Orforglipron (LY3502970) in Participants With Hypertension and Obesity or Overweight (ATTAIN-Hypertension) GZL2

NCT06952530 · tracked via the Priya Life Science Japan tracker
Phase
Phase 3
Started
2025-04-30
Last updated
2026-05-29

Condition(s) studied

Hypertension

Investigational drug(s) / intervention(s)

Orforglipron →Placebo

Orforglipron: Administered orally

Placebo: placebo administered

Study summary

GZL2 is an independent study conducted under the GZPL master protocol. GZL2 study will evaluate the efficacy and safety of orforglipron for treatment of hypertension in participants with obesity or overweight.

Eligibility

Sex
ALL
Min age
18 Years
Max age
—
Healthy volunteers
No
Inclusion Criteria: * refer to the GZPL master protocol study for screening eligibility. Exclusion Criteria: * refer to the GZPL master protocol study for screening eligibility.

Primary outcome measure(s)

  • Change from Baseline in office Systolic Blood Pressure (SBP) — Baseline to Week 36

Trial sites (99)

FacilityCityRegionStatus
Elite Clinical Studies, LLC Phoenix Arizona
Valley Clinical Trials, Inc. Covina California
Valley Clinical Trials, Inc. Northridge California
Chase Medical Research, LLC Waterbury Connecticut
Excel Medical Clinical Trials Boca Raton Florida
Care Access - Brandon Brandon Florida
Northeast Research Institute - Downtown Office Jacksonville Florida
Peace River Cardiovascular Center Port Charlotte Florida
East-West Medical Research Institute Honolulu Hawaii
Sinai Hospital Of Baltimore Baltimore Maryland
Ascension Saint Agnes Heart Care Baltimore Maryland
Lucida Clinical Trials New Bedford Massachusetts
Arcturus Healthcare , PLC, Troy Internal Medicine Research Division Troy Michigan
StudyMetrix Research City of Saint Peters Missouri
Excel Clinical Research, LLC Las Vegas Nevada
Palm Research Center Sunset Las Vegas Nevada
Rochester Clinical Research, LLC Rochester New York
Remington-Davis, Inc Columbus Ohio
Advanced Research Institute - Tigard Tigard Oregon
Care Access - Mauldin Mauldin South Carolina
Dallas Heart and Vascular Consultants, PA Duncanville Texas
Texas Institute of Cardiology, PA McKinney Texas
North Hills Family Medicine/North Hills Medical Research North Richland Hills Texas
Advanced Research Institute Ogden Utah
Carient Heart & Vascular - Manassas Manassas Virginia
Health Research of Hampton Roads, Inc. Newport News Virginia
National Clinical Research, Inc Richmond Virginia
Eastside Research Associates Redmond Washington
Instituto Médico Especializado (IME) Buenos Aires Argentina
CIPREC Buenos Aires Argentina
CIPREC Buenos Aires Argentina
CEMEDIC Buenos Aires Argentina
Instituto de Investigaciones Clínicas Córdoba Córdoba Argentina
Centro de Investigaciones Clínicas Baigorria Granadero Baigorria Argentina
INECO Neurociencias Oroño Rosario Argentina
Instituto Médico Fundación Grupo Colaborativo Rosario Investigación y Prevención Medica Rosario Argentina
Santa Maria de la Salud Centro Medico San Isidro Argentina
Beijing Pinggu District Hospital Beijing China
China-Japan Union Hospital Changchun China
Changde First People's Hospital Changde China

+ 59 more sites — see the full list on the official registry below.

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06952530 on ClinicalTrials.gov ↗ ← All trials in Japan