Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-24 @ 2:03 PM
Ignite Modification Date:
2025-12-24 @ 2:03 PM
NCT ID:
NCT06205095
Eligibility Criteria:
Inclusion Criteria:
1. Patient capable of providing informed consent;
2. Female patients with HMB over the age of 18 years, for whom prophylactic treatment with Wilate® is deemed clinically appropriate according to the medical discretion (based on their expert opinion given consideration of the patient's bleeding history and responsiveness to treatment) of the treating hemostasis-focused physician practicing at a Hemophilia Treatment Center;
3. Modified PBAC score \> 100 at screening;
4. Patients with a diagnosis of inherited von Willebrand disease (any type);
5. Stable treatment for HMB and iron deficiency anemia for 3 cycles before entering the study and anticipated to remain unchanged for the duration of the study;
6. Patients willing to have an infusion administered by a nurse over the course of the study period;
7. Patients who agree to use only the feminine hygiene products supplied by the sponsor.
Exclusion Criteria:
1. Diagnosed with any other known bleeding disorder;
2. Pregnancy or plans to become pregnant within the duration of the study;
3. Breastfeeding or plans to breastfeed within the duration of the study;
4. Known hypersensitivity reactions to human plasma-derived products or any ingredient in the formulation;
5. Known antibodies to VWF or FVIII;
6. Severe liver disease;
7. Anticipated initiation of the following: oral, transdermal, injectable, and vaginal ring hormonal contraceptives; GnRH analogues; or a hormonal intrauterine device (IUD) within the study period;
8. Anticipated elective procedure that is expected to require intensive treatment with VWF or FVIII for \>10 days during the study period;
9. Patients with \>2 risk factors for VTE (risk factors are determined at discretion of treating physician) or recent history of thrombosis (i.e. within the last year).
10. Patient concurrently receiving desmopressin (desmopressin cannot be taken concurrently with Wilate®, except for in the context of escalation treatment for excessive bleeding).
11. Anticipated initiation of any new therapies for the treatment of heavy menstrual bleeding 3 weeks prior to enrollment
Healthy Volunteers:
False
Sex:
FEMALE
Minimum Age:
18 Years
Study:
NCT06205095
Study Brief:
Protocol Section:
NCT06205095