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Willebrand International Non-interventional Global Surveillance

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LFB

Status

Completed

Conditions

Von Willebrand Disease

Study type

Observational

Funder types

Industry

Identifiers

Details and patient eligibility

About

Collect information about WILLFACT or WILFACTIN in their real life clinical use and identify the therapeutic practices in an international environment.

Full description

Non-interventional, prospective, non comparative, international, multicentre study.

Enrollment

80 patients

Sex

All

Volunteers

No Healthy Volunteers

Inclusion criteria

  • Patients with inherited von Willebrand disease
  • Patients treated with WILLFACT or WILFACTIN
  • Patient or parent/legal representative who has provided written signed and dated informed consent before any data collection.

Exclusion criteria

  • Patients who usually do not keep injection log up to date, when treated.

Trial design

80 participants in 1 patient group

Von Willebrand factor deficient patient
Description:
Inherited von Willebrand disease

Trial contacts and locations

18

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Data sourced from clinicaltrials.gov

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