Recruiting

Emicizumab vs. Factor VIII

Sponsor:

Wayne State University

Code:

NCT05022459

Conditions

Hemophilia A

Eligibility Criteria

Sex: All

Age: 6 - 19

Healthy Volunteers: Not accepted

Interventions

Emicizumab

FVIII

Study Details

Brief summary:

Hemophilia A (HA) is a genetic bleeding disorder resulting from a deficiency or absence of factor VIII (FVIII), which is necessary in the clotting process. This disorder occurs mostly in males and in severe cases causes frequent bleeding episodes in joints and muscles which can lead to progressive damage that affects mobility and quality of life. Prophylactic FVIII administered intravenously every other day has been the standard of care treatment for HA for the past few decades.

Sports and physical activity are generally encouraged in patients with hemophilia on appropriate prophylactic treatment to increase strength, prevent or decrease obesity, accrue and maintain bone density and encourage normal socialization. To ensure safety with participation in sports in persons with hemophilia A (PWHA), timing of FVIII administration is often adjusted to maximize FVIII at the time of sports. The exact factor level that is needed to safely participate in sports and minimize bleeding risk is not yet known. Based on clinical practice, infusion of FVIII to near the lower limit of normal right before participation in sports generally works to prevent bleeding.

The study is looking at how well the newly approved medication Emicizumab works compared to Factor VIII to prevent bleeding in patients with Hemophilia A who play sports. The study will enroll children and adolescents who are already on Emicizumab or Factor VIII who are currently playing sports.

Conditions

Hemophilia A

Study ID

NCT05022459

Start date

Aug 16, 2023

Status verified date

Jun, 2026

Completion date

Mar, 2029

Anticipated

Primary completion date

Jan, 2029

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 6 - 19

Healthy Volunteers: Not accepted

Inclusion Criteria:

1. Participant (if 18 years of age or older) or parent/LAR is willing and able to provide written informed consent; minor participant is willing and able to provide assent, if applicable based on site and local regulations
2. Males and females between 6 to ≤ 19 years of age at time of enrollment with moderate to severe Hemophilia A (FVIII activity ≤ 5%) without inhibitors are eligible for participation in this study
3. Participants must be on Emicizumab or standard FVIII prophylaxis per institutional/primary hematologist recommendations
4. Participants must be engaging in or registered to start participating in one or more sports activities with moderate to high risk of bleeding as defined by the NHF- Playing it Safe guidelines (numerical rating >/= 2).
5. Participant must be willing to keep activity, bleed, and treatment logs for the duration of the study

Exclusion Criteria:

1. Participant/parent/LAR unwilling to provide informed consent/assent
2. Unwilling to log or document bleeds and treatment information as per study guidelines
3. Participants with any other bleeding disorders will be excluded
4. Patients who are pregnant, planning to become pregnant, or breastfeeding should not be enrolled in the study
5. Participants on concomittent FVIII replacement and emicizumab for sports participation

Study Design

Enrollment

72 participants

Anticipated

Interventions and Outcome Measures

Arms

Emicizumab Prophylaxis

This group will include patients on standard of care Emicizumab prophylaxis for Hemophilia A

FVIII Prophylaxis

This group will include patients on standard of care FVIII prophylaxis for Hemophilia A

Interventions

Emicizumab

Patients in this group will be on standard of care Emicizumab prophylaxis for Hemophilia A

FVIII

Patients in this group will be on standard of care FVIII prophylaxis for Hemophilia A

Primary outcome measure

  • Number of bleeds [ Time Frame: 2 years ]

Central Contacts and Locations

Central contacts

Locations

Arkansas Children's Hospital

Recruiting

Little Rock, Arkansas, United States, 72202

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Stanford University

Recruiting

Palo Alto, California, United States, 94304

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Rady Children's Hospital

Recruiting

San Diego, California, United States, 92123

Contacts

Principal Investigator:

Kelly Bush, MD

Johns Hopkins All Children's Hospital

Recruiting

St. Petersburg, Florida, United States, 33701

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Rush University Children's Hospital

Recruiting

Chicago, Illinois, United States, 60612

Contacts

Indiana Hemophilia & Thrombosis Center

Recruiting

Indianapolis, Indiana, United States, 46260

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Boston Children's Hospital

Recruiting

Boston, Massachusetts, United States, 02215

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Children's Hospital of Michigan

Recruiting

Detroit, Michigan, United States, 48201

Contacts

Amy Stolinski, MPH

STEPStudy@wayne.edu

Cincinnati Children's Hospital Medical Center

Recruiting

Cincinnati, Ohio, United States, 45229

Contacts

Amy Stolinski, MPH

stepstudy@wayne.edu

Oklahoma Center for Bleeding and Clotting Disorders

Recruiting

Oklahoma City, Oklahoma, United States, 73104

Contacts

Principal Investigator:

Osman Khan, MD

More Information

Sponsor

Wayne State University

Last update posted

Jul 2, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-26. This information was provided to ClinicalTrials.gov by Wayne State University on 2026-07-02. Recruitment status is synced daily from ClinicalTrials.gov and may not reflect the sponsor's current status. Confirm during your call.