A Study to Learn More About Treatment With Damoctocog Alfa Pegol, How it is Used in Every Day Practice ("Real-World"), and How Satisfied People Who Receive Damoctocog Alfa Pegol Are in United States (US) Hemophilia Treatment Centers

NCT05395858 | Terminated

• 1 other identifier: 21280
• Study Type: observational
• Target: 14
• Locations: 1 country
• Sites: 3

Brief Summary

People with hemophilia A do not have enough of a protein found naturally in the blood called "clotting factor 8", also known as FVIII. This protein helps the blood to clump together to prevent and stop bleeding. People with lower levels of FVIII or FVIII that does not work properly may bleed for a long time from minor wounds, bleed into their joints, or have internal bleeding. The study treatment, Jivi (also called damoctocog alfa pegol), is already available as a treatment for people aged 12 years and older with hemophilia A, to help prevent bleeding, also known as "prophylactic" treatment. It works by replacing the missing FVIII, or the FVIII that does not work properly. It can also be used to stop bleeding that has already occurred and prior to surgery to prevent bleeding. The main goal of this study is to learn how damoctocog alfa pegol is used in the "real world" as a treatment in the United States (US) and how well it works and what other treatments patients use while receiving damoctocog alfa pegol treatment. It will also determine how satisfied people are with the treatment. There will be no required visits with a study doctor in this study. The study will include about 20 male or female patients in the US aged 12 years and over who have hemophilia A. All the patients in this study will have switched from their previous FVIII replacement treatment to damoctocog alfa pegol. While the patients are receiving damoctocog alfa pegol, they will complete a survey to say how they feel about the treatment. Their doctors will also record information about their treatment with damoctocog alfa pegol and how well it is working. This study will collect information from the patients' medical records and surveys. They will use this information to find out more about treatment with damoctocog alfa pegol under "real world" conditions. They will look at:

• how often the patients receive damoctocog alfa pegol and how much they use
• what other treatments the patients received before receiving damoctocog alfa pegol, how they used it and how much they used
• how well damoctocog alfa pegol works at preventing bleeding, and how it compares to previous products used.

Conditions

Hemophilia A

Keywords

Bleeding disorder; Coagulation factor VIII; Blood Coagulation Disorders

Outcome Measures

Primary Outcomes (1)

• Frequency of damoctocog alfa pegol infusions

  Reported as infusions. IRB: institutional review board

  From index date through the date of central IRB approval (3 years and 8 months)

Secondary Outcomes (7)

• Descriptive summary of pre-damoctocog alfa pegol treatment regimen

  6 months prior to the index date.

• Descriptive summary of damoctocog alfa pegol treatment regimen.

  Up to 5 years from index date

• Descriptive summary of post-damoctocog alfa pegol treatment regimen, if applicable.

  Up to 4 years

• Descriptive summary of changes in pre-damoctocog alfa pegol treatment regimes

  6 months prior to the index date.

• Descriptive summary for reasons for treatment discontinuation of pre-damoctocog alfa pegol treatment regimes.

  6 months prior to the index date.

Study Arms (1)

Hemophilia A patients

Patients will be identified via standard medical charts or electronic medical records (EMRs).

Other: No intervention

Interventions

No intervention OTHER

Retrospective analysis using database without any intervention assigned in the study.

Hemophilia A patients

Eligibility Criteria

• Age: 12 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Child (0-17), Adult (18-64), Older Adult (65+)
• Sampling Method: Non-Probability Sample

Study Population

United States patients aged ≥12 years diagnosed with hemophilia A (congenital FVIII deficiency) who switched from a previous FVIII replacement treatment to damoctocog alfa pegol. No investigational products will be administered in this study.

You may qualify if:

• Male or female with a diagnosis of hemophilia A
• Previously or currently treated with damoctocog alfa pegol for at least 6 months.
• Treated with damoctocog alfa pegol per the US approved label to include:
• Aged ≥12 years at the time of damoctocog alfa pegol treatment initiation
• Previously treated for hemophilia A with an FVIII replacement therapy other than damoctocog alfa pegol
• Treatment modality of on-demand, prophylactic, intermittent prophylaxis or a combination thereof
• Have data in the medical record at the participating site as follows:
• For a minimum of 6 months prior to the damoctocog alfa pegol initiation date
• For a minimum of 6 months post-damoctocog alfa pegol initiation date AND the patient was receiving treatment with damoctocog alfa pegol during this 6-month follow-up period AND this data is dated prior to the central institutional review board (IRB) approval date for the study
• To include the FVIII replacement therapy most recently received prior to the initiation of damoctocog alfa pegol
• For patients in the prospective cohort
• Signed informed consent
• Current treatment with damoctocog alfa pegol or discontinued use of damoctocog alfa pegol within 3 months prior to the date of enrollment into the retrospective cohort.

You may not qualify if:

• Diagnosis of any other bleeding/coagulation disorder other than hemophilia A.
• Participation in any past or current damoctocog alfa pegol interventional trial.

Sponsors & Collaborators

• Bayer: lead

Study Sites (3)

University of California, Davis

Sacramento, California, 95817, United States

Location

Tulane University

New Orleans, Louisiana, 70112, United States

Location

Regents of the University of Minnesota

Minneapolis, Minnesota, 55455, United States

Location

Related Links

• Click here to find information for studies related to Bayer products. To find this study enter the ClinicalTrials.gov identifier (NCT) number or Bayer Study Identifier (ID) in the search field.

MeSH Terms

Conditions

Hemophilia A; Hemostatic Disorders; Blood Coagulation Disorders

Condition Hierarchy (Ancestors)

Blood Coagulation Disorders, Inherited; Hematologic Diseases; Hemic and Lymphatic Diseases; Coagulation Protein Disorders; Hemorrhagic Disorders; Genetic Diseases, Inborn; Congenital, Hereditary, and Neonatal Diseases and Abnormalities; Vascular Diseases; Cardiovascular Diseases

Study Design

• Study Type: observational
• Observational Model: COHORT
• Time Perspective: RETROSPECTIVE
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: April 28, 2022
• First Posted: May 27, 2022
• Study Start: January 17, 2023
• Primary Completion: November 6, 2023
• Study Completion: November 6, 2023
• Last Updated: November 28, 2023

Record last verified: 2023-11

Data Sharing

• IPD Sharing: Will not share

Locations

US (3)