Patient Guide: A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of NXT007 in Persons With Severe or Moderate Hemophilia A

Why Use Quri.ai for This Trial?

  • ✓ Simplified eligibility checker - know if you qualify in minutes
  • ✓ Direct contact with study coordinators at 12 locations
  • ✓ Plain language explanations of medical terms and procedures
  • ✓ Personalized enrollment support throughout your journey
  • ✓ Free service - no hidden fees or obligations
Trial ID: NCTNCT05987449
Status: 🟢 Enrolling Now
Condition: Hemophilia A
Phase: PHASE1, PHASE2

Where You Can Participate

This study is available at 12 locations across the country.

Top locations include:
  • • Sacramento, California
  • • Washington, District of Columbia
  • • Indianapolis, Indiana
  • • And 9 more locations

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A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of NXT007 in Persons With Severe or Moderate Hemophilia A - Join Clinical Trial NCTNCT05987449

How to Join This Clinical Trial - NCTNCT05987449

Learn how to participate in this PHASE1, PHASE2 trial studying an investigational therapy for Hemophilia A. This study is currently enrolling participants.

Am I Eligible for This Clinical Trial?

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

Condition Being Studied
Hemophilia A
Treatment Being Tested
Investigational treatment
Study Phase
PHASE1, PHASE2 - Safety and effectiveness study
Enrollment Status
Currently enrolling participants
Study Identifier
NCTNCT05987449 - 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 12 locations. Find a study site near you:

Clinical Research Site

Sacramento, California 95817 - United States

Status: RECRUITING

Clinical Research Site

Washington, District of Columbia 20007 - United States

Status: WITHDRAWN

Clinical Research Site

Indianapolis, Indiana 46260 - United States

Status: RECRUITING

Clinical Research Site

Iowa City, Iowa 52242 - United States

Status: RECRUITING

Clinical Research Site

Vancouver, British Columbia V6H 3N1 - Canada

Status: RECRUITING

Clinical Research Site

Hamilton, Ontario L8N 3Z5 - Canada

Status: RECRUITING

Clinical Research Site

Rozzano (MI), Lombardia 20089 - Italy

Status: RECRUITING

Clinical Research Site

Auckland, 1023 - New Zealand

Status: RECRUITING

Clinical Research Site

Gda?sk, 80-214 - Poland

Status: RECRUITING

Clinical Research Site

Warsaw, 02-776 - Poland

Status: RECRUITING

And 2 more locations available. Contact us to find the nearest participating site.

How to Enroll in This Study

To learn more about participating in this PHASE1, PHASE2 clinical trial for Hemophilia A:

  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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