Patient Guide: Research Study to Look at How Well the Drug Concizumab Works in Your Body if You Have Haemophilia Without Inhibitors

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 81 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT04082429
Status: ACTIVE_NOT_RECRUITING
Condition: Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors
Phase: PHASE3

Where You Can Participate

This study is available at 81 locations across the country.

Top locations include:
  • • Los Angeles, California
  • • Orange, California
  • • Detroit, Michigan
  • • And 78 more locations

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Research Study to Look at How Well the Drug Concizumab Works in Your Body if You Have Haemophilia Without Inhibitors - Join Clinical Trial NCTNCT04082429

How to Join This Clinical Trial - NCTNCT04082429

Learn how to participate in this PHASE3 trial studying an investigational therapy for Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors. Current status: ACTIVE_NOT_RECRUITING.

Am I Eligible for This Clinical Trial?

This clinical research study is looking for participants with Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors. Eligibility requirements include specific age ranges, health status, and medical history. Contact the study team to learn if you qualify.

Condition Being Studied
Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors
Treatment Being Tested
Investigational treatment
Study Phase
PHASE3 - Large-scale efficacy study
Enrollment Status
ACTIVE_NOT_RECRUITING
Study Identifier
NCTNCT04082429 - 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 81 locations. Find a study site near you:

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

Detroit, Michigan 48201 - United States

Status: Contact for availability

Clinical Research Site

Hershey, Pennsylvania 17033 - United States

Status: Contact for availability

Clinical Research Site

Nashville, Tennessee 37212 - United States

Status: Contact for availability

Clinical Research Site

San Antonio, Texas 78229 - United States

Status: Contact for availability

Clinical Research Site

Milwaukee, Wisconsin 53226 - United States

Status: Contact for availability

Clinical Research Site

Algiers, 16000 - Algeria

Status: Contact for availability

Clinical Research Site

Constantine, 25000 - Algeria

Status: Contact for availability

Clinical Research Site

Melbourne, Victoria 3004 - Australia

Status: Contact for availability

And 71 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 Haemophilia A Without Inhibitors, Haemophilia B Without Inhibitors:

  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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