Patient Guide: Special Use-results Surveillance on Long Term Use of Sogroya® in Children With Short Stature Due to Growth Hormone Deficiency Where Epiphysial Discs Are Not Closed

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 47 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT06109935
Status: ENROLLING_BY_INVITATION
Condition: Growth Hormone Deficiency in Children
Phase: Research Study

Where You Can Participate

This study is available at 47 locations across the country.

Top locations include:
  • • Asahikawa, Hokkaido,
  • • Beppu-shi, Oita-ken,
  • • Fukuoka-shi, Fukuoka-ken,
  • • And 44 more locations

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Special Use-results Surveillance on Long Term Use of Sogroya® in Children With Short Stature Due to Growth Hormone Deficiency Where Epiphysial Discs Are Not Closed - Join Clinical Trial NCTNCT06109935

How to Join This Clinical Trial - NCTNCT06109935

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

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
Clinical trial phase - Research study
Enrollment Status
ENROLLING_BY_INVITATION
Study Identifier
NCTNCT06109935 - 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 47 locations. Find a study site near you:

Clinical Research Site

Asahikawa, Hokkaido, 078-8510 - Japan

Status: Contact for availability

Clinical Research Site

Beppu-shi, Oita-ken, 874-0011 - Japan

Status: Contact for availability

Clinical Research Site

Fukuoka-shi, Fukuoka-ken, 814-0133 - Japan

Status: Contact for availability

Clinical Research Site

Fukuoka-shi, Fukuoka, 812-8582 - Japan

Status: Contact for availability

Clinical Research Site

Fukuoka, 830-0011 - Japan

Status: Contact for availability

Clinical Research Site

Gifu, 501-1194 - Japan

Status: Contact for availability

Clinical Research Site

Gunma, 373-8585 - Japan

Status: Contact for availability

Clinical Research Site

Hachioji-shi, Tokyo-to, 192-0919 - Japan

Status: Contact for availability

Clinical Research Site

Hamamatsu-shi, Shizuoka, 431-3192 - Japan

Status: Contact for availability

Clinical Research Site

Higashimatsuyama-shi, Saitama-ken, 355-0008 - Japan

Status: Contact for availability

And 37 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this 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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