Patient Guide: To Assess the Efficacy, Safety, and Tolerability of INCB000928 in Participants With Fibrodysplasia Ossificans Progressiva

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 29 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05090891
Status: 🟢 Enrolling Now
Condition: Fibrodysplasia Ossificans Progressiva (FOP)
Phase: PHASE2

Where You Can Participate

This study is available at 29 locations across the country.

Top locations include:
  • • San Francisco, California
  • • Rochester, Minnesota
  • • Philadelphia, Pennsylvania
  • • And 26 more locations

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To Assess the Efficacy, Safety, and Tolerability of INCB000928 in Participants With Fibrodysplasia Ossificans Progressiva - Join Clinical Trial NCTNCT05090891

How to Join This Clinical Trial - NCTNCT05090891

Learn how to participate in this PHASE2 trial studying an investigational therapy for Fibrodysplasia Ossificans Progressiva (FOP). This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Fibrodysplasia Ossificans Progressiva (FOP). 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 (FOP)
Treatment Being Tested
Investigational treatment
Study Phase
PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05090891 - 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 29 locations. Find a study site near you:

Clinical Research Site

San Francisco, California 94143 - United States

Status: WITHDRAWN

Clinical Research Site

Rochester, Minnesota 55905 - United States

Status: RECRUITING

Clinical Research Site

Philadelphia, Pennsylvania 19104 - United States

Status: RECRUITING

Clinical Research Site

Philadelphia, Pennsylvania 19104 - United States

Status: RECRUITING

Clinical Research Site

Ciudad Autonoma Buenos Aires, C1199ABB - Argentina

Status: NOT_YET_RECRUITING

Clinical Research Site

St Leonards, New South Wales 02065 - Australia

Status: COMPLETED

Clinical Research Site

Parkville, Victoria 03052 - Australia

Status: RECRUITING

Clinical Research Site

San Paolo, 05652-900 - Brazil

Status: RECRUITING

Clinical Research Site

Toronto, Ontario M5G 2C4 - Canada

Status: RECRUITING

Clinical Research Site

Santiago, 7501126 - Chile

Status: RECRUITING

And 19 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE2 clinical trial for Fibrodysplasia Ossificans Progressiva (FOP):

  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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