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NCT Number: NCT05981274

A Study on the Bone-health Effectiveness of Applying Recombinant Factor VIII Fc (rFVIIIFc) to Patients With Hemophilia A (Prototype A)

Study Objectives*

1. Provide a systematic evaluation of the treatment outcomes in patients with hemophilia A 2. Emphasize the importance and clinical benefits of rFVIII-Fc in joint and bone health. 3. Compare the clinical outcomes from 1 year before and after switching to EHL. 4. Exploratory: Identify biomarkers that could provide more useful and convenient evaluations of joint and bone health. (Time-saving and easy to monitor)

Recruiting

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Key information

Sex eligibility

Male

Study type

Observational

Primary location

Tri-Service General Hospital Hemophilia Care Center

Taipei, Neihu Dist., 114202, Taiwan

Location status: Recruiting

Location contact

Yeu-Chin chen

CONTACT

[email protected]

(+886)2-87923311 ext. 13654

About this study

In this study, we would like to focus on the evaluation of joint and bone health in persons with severe hemophilia A (PwHA) treated with rFVIIIFc prophylaxis. We also aim to identify potential biomarkers for assessing the joint and bone health of PwHA. Since the joint and bone health examinations are time-consuming, expensive, and require special equipment, the patients could only receive the examinations annually to realize the status of their joint health. The biomarkers testing will provide a more convenient and time-saving option on the joint and bone health evaluation for PwHA. Therefore, surrogate of biochemical marker(s) to represent the joint and BMD progression is an unmet need for clinical practice. Investigating different biomarkers and combining them with the joint and BMD results to provide a systematic approach for elucidating the treatment outcomes of PwHA treated with rFVIIIFc is major goal of this study.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Patients with severe hemophilia A (all ages).
  • Patients with moderate type hemophilia A with hemophilic arthropathy.
  • Currently on rFVIIIFc regular prophylaxis and have previous medical record with regular prophylaxis with standard half-life product for one year
  • Able and willing to undergo joint and bone examinations

Exclusion criteria

  • Participants of other interventional studies.
  • Patients with current inhibitors.
  • History of major neurological disease (eg. Stroke, Parkinson's disease, neuropathy, etc.)
  • History of major psychiatric disease (eg. Schizophrenia, bipolar disorder)
  • Significantly impaired vision/hearing

Treatment and study plan

serum biomarker.

Diagnostic Test

serum biomarker:CTX-II, COMP, hsCRP, TNF-a, CTX-I, sRANKL, OPG, and Osteopontin (OPN)

Primary outcomes

  1. Systematic joint and bone health assessments before and after enrollment

    Time frame: up to 5 years

    Haemophilia Early Arthropathy Detection with Ultrasound (HEAD-US) on patients' ankles, knees, and elbows. Also evaluate the Hemophilia Joint Health Score (HJHS) and Dexa scan at the hip.

Secondary outcomes

  1. Serum markers

    Time frame: up to 5 years

    CTX-II, COMP, HSCRP, TNF-ALPHA, CTX-I, SRANKL, OPG, OPN

Study contacts

Contact information is provided by the study sponsor or research team.

Yeu-Chin Chen

CONTACT

[email protected]

(+886)2-87923311 ext. 13654

Sponsors and collaborators

Lead sponsor

Tri-Service General Hospital (TSGH)

Other

Registry information

Official study title

A Prospective and Retrospective Interventional Study on the Bone-health Effectiveness of Applying Recombinant Factor VIII Fc (rFVIIIFc) to Patients With Hemophilia A (Prototype A)

Important dates

Study start
2023
Primary completion
2027
Study completion
2027
First posted
Aug 8, 2023
Registry last updated
Apr 10, 2024

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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