Patient Guide: Study of Efficacy and Safety of LCZ696/Amlodipine in Grade 1 and 2 Hypertension Patients Uncontrolled by LCZ696 Monotherapy

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 43 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06236061
Status: ACTIVE_NOT_RECRUITING
Condition: Hypertension
Phase: PHASE3

Where You Can Participate

This study is available at 43 locations across the country.

Top locations include:
  • • Nagoya, Aichi
  • • Nagoya, Aichi
  • • Nagoya, Aichi
  • • And 40 more locations

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Study of Efficacy and Safety of LCZ696/Amlodipine in Grade 1 and 2 Hypertension Patients Uncontrolled by LCZ696 Monotherapy - Join Clinical Trial NCTNCT06236061

How to Join This Clinical Trial - NCTNCT06236061

Learn how to participate in this PHASE3 trial studying an investigational therapy for Hypertension. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Hypertension. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Hypertension
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT06236061 - ClinicalTrials.gov Identifier
Sponsored By
Study sponsor

What to Expect as a Participant

Participating in this clinical trial involves:

  • Initial screening to determine eligibility
  • Regular study visits and health assessments
  • Receiving the study treatment or placebo
  • Medical monitoring and follow-up care
  • Contributing to medical research that may help others
  • Potential access to new treatments before they're widely available

Clinical Trial Benefits and Compensation

Participants in this clinical research study may receive:

  • Close medical monitoring by healthcare professionals
  • Access to potential new treatments
  • Compensation for time and travel (varies by study)
  • No-cost study-related medical care
  • The opportunity to help advance medical knowledge

Where Is This Clinical Trial Located?

This study is enrolling participants at 43 locations. Find a study site near you:

Clinical Research Site

Nagoya, Aichi 451-8511 - Japan

Status: Contact for availability

Clinical Research Site

Nagoya, Aichi 453-0804 - Japan

Status: Contact for availability

Clinical Research Site

Nagoya, Aichi 454-0933 - Japan

Status: Contact for availability

Clinical Research Site

Nagoya, Aichi 457-8511 - Japan

Status: Contact for availability

Clinical Research Site

Itoshima, Fukuoka 819-1104 - Japan

Status: Contact for availability

Clinical Research Site

Chitose, Hokkaido 066-0032 - Japan

Status: Contact for availability

Clinical Research Site

Sapporo, Hokkaido 003-0026 - Japan

Status: Contact for availability

Clinical Research Site

Sapporo, Hokkaido 063-0826 - Japan

Status: Contact for availability

Clinical Research Site

Sapporo, Hokkaido 063-0842 - Japan

Status: Contact for availability

Clinical Research Site

Akashi, Hyogo 674-0081 - Japan

Status: Contact for availability

And 33 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE3 clinical trial for Hypertension:

  1. Review the eligibility criteria with your healthcare provider
  2. Contact the study team for a pre-screening interview
  3. Schedule an in-person screening visit if eligible
  4. Review and sign the informed consent form
  5. Begin participation in the clinical trial

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