Patient Guide: A Research Study in Children With a Low Level of Hormone to Grow. Treatment is Somapacitan Once a Week Compared to Norditropin® Once a Day (REAL4)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 96 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT03811535
Status: ACTIVE_NOT_RECRUITING
Condition: Growth Hormone Deficiency in Children
Phase: PHASE3

Where You Can Participate

This study is available at 96 locations across the country.

Top locations include:
  • • Birmingham, Alabama
  • • Los Angeles, California
  • • Orange, California
  • • And 93 more locations

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A Research Study in Children With a Low Level of Hormone to Grow. Treatment is Somapacitan Once a Week Compared to Norditropin® Once a Day (REAL4) - Join Clinical Trial NCTNCT03811535

How to Join This Clinical Trial - NCTNCT03811535

Learn how to participate in this PHASE3 trial studying an investigational therapy for Growth Hormone Deficiency in Children. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Growth Hormone Deficiency in Children
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT03811535 - 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 96 locations. Find a study site near you:

Clinical Research Site

Birmingham, Alabama 35233 - United States

Status: Contact for availability

Clinical Research Site

Los Angeles, California 90027 - United States

Status: Contact for availability

Clinical Research Site

Orange, California 92868 - United States

Status: Contact for availability

Clinical Research Site

Sacramento, California 95821 - United States

Status: Contact for availability

Clinical Research Site

Centennial, Colorado 80112 - United States

Status: Contact for availability

Clinical Research Site

Greenwood Village, Colorado 80111-2803 - United States

Status: Contact for availability

Clinical Research Site

Wilmington, Delaware 19803 - United States

Status: Contact for availability

Clinical Research Site

Aventura, Florida 33180 - United States

Status: Contact for availability

Clinical Research Site

Atlanta, Georgia 30318 - United States

Status: Contact for availability

Clinical Research Site

Indianapolis, Indiana 46202 - United States

Status: Contact for availability

And 86 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 Growth Hormone Deficiency in Children:

  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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