Patient Guide: A Study to Assess Safety, Tolerability and Efficacy of Garetosmab Versus Placebo Administered Intravenously (IV) in Adult Participants With Fibrodysplasia Ossificans Progressiva (FOP)

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 22 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05394116
Status: ACTIVE_NOT_RECRUITING
Condition: Fibrodysplasia Ossificans Progressiva
Phase: PHASE3

Where You Can Participate

This study is available at 22 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Nashville, Tennessee
  • • St Leonards, New South Wales
  • • And 19 more locations

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A Study to Assess Safety, Tolerability and Efficacy of Garetosmab Versus Placebo Administered Intravenously (IV) in Adult Participants With Fibrodysplasia Ossificans Progressiva (FOP) - Join Clinical Trial NCTNCT05394116

How to Join This Clinical Trial - NCTNCT05394116

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

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Fibrodysplasia Ossificans Progressiva
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT05394116 - 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 22 locations. Find a study site near you:

Clinical Research Site

Los Angeles, California 90095 - United States

Status: Contact for availability

Clinical Research Site

Nashville, Tennessee 37232 - United States

Status: Contact for availability

Clinical Research Site

St Leonards, New South Wales 2065 - Australia

Status: Contact for availability

Clinical Research Site

Sao Paulo, 05652-900 - Brazil

Status: Contact for availability

Clinical Research Site

Concepcion, Bio Bio 4030000 - Chile

Status: Contact for availability

Clinical Research Site

Shanghai, 200065 - China

Status: Contact for availability

Clinical Research Site

Chia, Cundinamarca 140013 - Colombia

Status: Contact for availability

Clinical Research Site

Helsinki, Stenbäckinkatu 11 00029 - Finland

Status: Contact for availability

Clinical Research Site

Montpellier, 34090 - France

Status: Contact for availability

Clinical Research Site

Paris, 75010 - France

Status: Contact for availability

And 12 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 Fibrodysplasia Ossificans Progressiva:

  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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