๐๏ธ Verified NIH Record โข Updated 2026-06-30
Evaluating Effectiveness and Long Term Safety of Damoctocog Alfa Pegol in Patients, Who Have Been Diagnosed With Hemophilia A (NCT03932201)
Observational Study Evaluating Effectiveness and Safety of Real-World Treatment With Damoctocog Alfa Pegol in Previously Treated Patients With Hemophilia A
๐ต Active, Not Recruiting Interventional Protocol ๐ Observational Clinical Research Sponsor: Bayer
๐ฉบ Plain-English Summary (8th-Grade Level)
The aim of the HEM-POWR study is to understand better how Damoctocog alfa pegol (Jivi) is used to treat people with Hemophilia A in day-to-day life, how well the treatment is tolerated and how satisfied patients and physicians are with the treatment.
Who can join: Review the eligibility criteria below.
Location: South Alabama Medical Science Foundation โ Mobile, Alabama
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (29 Sites)
Showing the first 25 of 29 sites.
- South Alabama Medical Science Foundation โ Mobile, Alabama
- Banner MD Anderson Cancer Center โ Phoenix, Arizona
- University California Davis โ Davis, California
- Orthopaedic Hospital DBA Orthopaedic Institute for Children โ Los Angeles, California
- The Center for Comprehensive Care and Diagnosis of Inherited Blood Disorders โ Orange, California
- University of Colorado Hemophilia and Thrombosis Center โ Aurora, Colorado
- Georgetown University โ Washington D.C., District of Columbia
- Tulane University โ New Orleans, Louisiana
- Regents of University of Minnesota โ Minneapolis, Minnesota
- East Carolina University - Brody School of Medicine โ Greenville, North Carolina
- Many locations โ Multiple Locations,
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๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Hemophilia A
- Study to Test the Safety and How Well Patients With Severe Hemophilia A Respond to Treatment With BAY 2599023 (DTX 201), a Drug Therapy That Delivers a Healthy Version of the Defective Factor VIII Gene Into the Nucleus of Liver Cells Using an Altered, Non-infectious Virus (AAV) as a "Shuttle" โ Little Rock, Arkansas
- Long-term Safety and Efficacy of Efanesoctocog Alfa (BIVV001) in Previously Treated Patients With Hemophilia A โ Los Angeles, California
- Gene Therapy Trial for Platelet Derived Factor VIII Production in Hemophilia A โ Milwaukee, Wisconsin
- A Long-term Study of ADYNOVI/ADYNOVATE in Participants With Haemophilia A โ Gainesville, Florida
- A Study to Evaluate Impact of Efanesoctocog Alfa on Long-term Joint Health in Participants With Hemophilia A โ Gilbert, Arizona
- Study to Evaluate the Efficacy and Safety of PF-07055480 / Giroctocogene Fitelparvovec Gene Therapy in Moderately Severe to Severe Hemophilia A Adults โ Mountain View, California
Explore by condition: All Hemophilia A clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.