Version Testing of EnzySystem Version A for Hemophilia A

Hemophilia A Clinical Trial

Official title:

Version Testing of EnzySystem Version A for Hemophilia A

Clinical Trial Details — Status: Recruiting

Administrative data

• NCT number: NCT06273865
• Other study ID #: HEMSTOL77
• Status: Recruiting
• Start date: May 29, 2024
• Est. completion date: December 15, 2024

Study information

• Verified date: February 2024
• Source: Radboud University Medical Center
• Contact: Aernoud Bavinck, Drs
• Phone: +31 24 361 1111
• Email: aernoud.bavinck[@]radboudumc.nl
• Is FDA regulated: No
• Study type: Observational

Clinical Trial Summary

Background of the study: To measure blood clotting, blood is taken from a vein. This blood is processed in the laboratory and then tested. A new device has been developed that requires only a very small volume of blood (5-10 drops of blood) to perform the laboratory tests. The long-term goal is that this device can be used by a doctor or at home to quickly measure blood clotting. In this research we want to compare this new system with the standard methods - measurement in the laboratory - and evaluate whether the correct value is determined. Objective of the study: The primary objective of this study is to demonstrate that the EnzySystem HemA version A can record thrombin generation TG and quantify FVIII activity levels within a time frame of 60 min in fresh whole blood samples of healthy volunteers and patients with hemophilia A in the Enzyre laboratory (for healthy volunteers) and the Radboudumc (for patients with hemophilia A). Study design: This is a cross-sectional observational study. All participants are asked to fill a questionnaire prior to blood collection. The blood of healthy volunteers will be collected in an office of Enzyre BV, the blood of patients will be collected in the Radboudumc. Blood collection, by venepuncture, will be conducted by a Radboudumc research nurse or physician of the research team in both locations. In total, four blood tubes with citrate as anticoagulant will be drawn (a total of around 11 mL). Study population: The study population consists of 20 healthy volunteers: evenly distributed between male and female; ages spread over the range from 20 to 70 years old; recruited by Enzyre via advertisement. 20 Patients: 5 severe hemophilia A; 5 moderate hemophilia A; 10 mild hemophilia A; recruited from the Hemophilia Treatment Center (HTC) Nijmegen-Eindhoven-Maastricht (NEM) (location Radboudumc). Primary study parameters/outcome of the study: Demonstrate that the EnzySystem HemA version A can record TG and quantitative FVIII activity levels within a time frame of 60 min in fresh blood samples of healthy volunteers and patients with hemophilia A. Secondary study parameters/outcome of the study (if applicable): Secondary study parameters are composed whether the measured values comply with the desired assay specificity and accuracy. Outcomes are analysed for equivalence compared to one-stage FVIII assay, FVIII chromogenic assay, thrombin generation via the Nijmegen Hemostasis Assay, and possibly via the Technoclone assay. Is it possible to measure FVIII activity with the EnzySystem HemA version A in fresh blood samples of healthy volunteers and patients with hemophilia A, compared to the gold standard with; - Precision in the normal range (60-140%): min. 30% - Precision in the low range (3-10%): min. 50% - Limit of Detection range min. 100 % FVIII activity - Limit of Detection low range min. 3 % FVIII activity Is it possible to measure TG with the EnzySystem HemA version A in fresh blood samples of healthy volunteers and patients with hemophilia A, compared to the gold standard with; - Precision in the normal range (60-140%) of control samples: min. 30% - Precision in patient with hemophilia A: min. 50% - Limit of Detection, high range > 400 nM thrombin activity - Limit of Detection measured with Plasma, low range < 50 nM thrombin Other study parameters All samples will also be tested for other hemostasis specific parameters as these parameters may affect a proper measurement of both FVIII activity and Thrombin Generation. The following parameters will be measured in plasma obtained from the whole blood vacutainers. Moreover, left over samples (plasma) will eventually be used to develop other coagulation related parameters. - von Willebrand Factor antigen levels - von Willebrand Factor ristocetin activity levels - Prothrombin Fragment 1+2 levels - ADAMTS13 activity - FVIII antigen levels - blood group

Recruitment information / eligibility

• Status: Recruiting
• Enrollment: 40
• Est. completion date: December 15, 2024
• Est. primary completion date: October 15, 2024
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: All
• Age group: 20 Years to 70 Years

Eligibility

Inclusion Criteria:

Healthy volunteers:

• Age between 20 to 70 years old (equally distributed over the age range)
• 7 volunteers 20-40 years old
• 7 volunteers 40-60 years old
• 6 volunteers 60+ years old

Hemophilia A patients:

• Diagnosed with mild (FVIII activity levels 5-40%), moderate (FVIII activity levels 1-5%) or severe hemophilia A (FVIII activity levels <1%)
• Medication

1. On demand treatment

2. Washout of medication of at least 24 hours after treatment with short half life (SHL) replacement therapy

3. Washout of medication of at least 72 hours after treatment with extended half life (EHL) replacement therapy

• Age 20-70 years old Exclusion Criteria: A healthy volunteer who meets any of the following criteria will be excluded from

participation in this study:

• use of anticoagulants or platelet antagonists (aspirin or any TAR);
• known allergy to stainless steel;
• trauma or surgery within the last two weeks;
• pregnancy;
• use of:
• NSAIDs;
• antimicrobial medication;
• thyroid inhibitors; or SSRI's. A hemophilia A patient who meets any of the

following criteria will be excluded from participation in this study:

• use of anticoagulants or platelet antagonists (aspirin or any TAR);
• known allergy to stainless steel;
• trauma or surgery within the last two weeks;
• a bleeding episode within the last two weeks;
• clinical indication of liver cirrhosis (echographic indication, enlarged spleen, decreased platelet count);
• pregnancy;
• FVIII inhibitors;
• Signs of inflammation or infection
• use of:
• NSAIDs;
• antimicrobial medication;
• thyroid inhibitors or SSRI's;
• Emicizumab.

Related Conditions & MeSH terms

• Hemophilia A

Intervention

Diagnostic Test:
• Several assays
Standard blood draw by venipuncture is performed in all study participants to collect blood samples in four 2.7 mL citrated blood tubes. Tube one is a dummy tube and is discarded. Tube two is used for the FVIII activity and thrombin generation assay on the EnzySystem. Tube three is used to perform conventional FVIII activity and thrombin generation assays. Tube four is used for duplicate measurements of the conventional assays and measurement of prothrombin F1+2 antigen levels, ADAMTS13 activity, FVIII antigen, VWF (von Willebrand Factor) antigen and von Willebrand ristocetin cofactor activity levels.

Locations

Country	Name	City	State
Netherlands	Enzyre BV	Nijmegen	Gelderland
Netherlands	Radboud university medical center	Nijmegen

Sponsors (2)

Lead Sponsor	Collaborator
Radboud University Medical Center	Enzyre B.V.

Country where clinical trial is conducted

Netherlands, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Time between venipuncture and EnzySystem assay results	Time is measured between venipuncture, start of the EnzySystem FVIII activity and thrombin generation assay, and assay results	All measurements with the EnzySystem will be performed <2 hours of drawing blood
Secondary	Validity of EnzySystem FVIII activity results	Comparison of the FVIII activity results obtained with the EnzySystem and with conventional (one-stage and chromogenic) assays	All steps until freezing of the plasma should take place within two hours after venipuncture
Secondary	Validity of EnzySystem thrombin generation results	Comparison of the thrombin generation results obtained with the EnzySystem and with conventional assays	All steps until freezing of the plasma should take place within two hours after venipuncture