Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Efficacy, Safety & Utilisation of Nuwiq, Octanate and Wilate in Previously Untreated & Minimally Treated Haemophilia A Patients
NCT03695978 · View on ClinicalTrials.gov ↗
Study Summary
International, post-authorisation non-interventional study to evaluate real-life effectiveness, safety and utilisation patterns of Octapharma's FVIII concentrates Nuwiq, Octanate, and Wilate in previously untreated and minimally treated severe haemophilia A patients in routine clinical practice.
Conditions Studied
Study Locations (20)
Other
- CENIDOR — Salta
- Azerbaijan State Advanced Training Institute for Doctors Hematology Department Scientific-Research Center of Hemophilia — Baku
- Republican Scientific Center for Radiation Medicine and Human Ecology — Homyel
- Republican Scientific and Practical Centre of Children Oncology, Hematology and Immunology — Minsk
- Hôpital Universitaire des Enfants Reine Fabiola — Brussels
- Cliniques Universitaires Saint-Luc — Brussels
- Cliniques Universitaires Saint-Luc — Brussels
- Department of Hematology Research Research Transition Facility — Edmonton
- University Hospital Centre Zagreb — Zagreb
- Tallinn Childrenś Hospital Clinic of Paediatric Department of Haematology and Oncology — Tallinn
- CENTRE HOSPITALIER UNIVERSITAIRE de BESANCON — Besançon
- CHRU Tours - Hôpital Trousseau — Chambray-lès-Tours
- Centre Régional de Traitement de l'hémophilie — Le Mans
- Hopital Simone Veil Groupement Hospitalier Eaubonne-Montmorency — Montmorency
- CHU Hotel Dieu, Centre de Traitment de l'Hemophilie — Nantes
- Hôspital Necker Enfants Malades — Paris
Florida
- University of Miami Miller School of Medicine — Miami
Louisiana
- Ochsner Clinic Foundation — New Orleans
Nevada
- Cure 4 The Kids Foundation Children's Specialty Center — Las Vegas
Ontario
- McMaster University, Division of Pediatric Hematology/Oncology Room 3N27 — Hamilton
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 200 participants |
| Start Date | 2018-02-13 |
| Est. Completion | 2030-06 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03695978
The ClinicalTrials.gov registry entry for NCT03695978 describes a study currently listed as recruiting. It is categorized as an unspecified phase, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 200 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Octapharma, which has 73 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Haemophilia A appearing as the primary indexed condition, and to 0 interventions. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT03695978 reports 20 study locations spanning 5 distinct geographic areas — top geographies include Other, Florida, Louisiana. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT03695978 about?
NCT03695978 is a clinical study titled "Efficacy, Safety & Utilisation of Nuwiq, Octanate and Wilate in Previously Untreated & Minimally Treated Haemophilia A Patients". International, post-authorisation non-interventional study to evaluate real-life effectiveness, safety and utilisation patterns of Octapharma's FVIII concentrates Nuwiq, Octanate, and Wilate in previously untreated and minimally treated severe haemophilia A patients in routine clinical practice.
What is the current status of trial NCT03695978?
This trial is currently recruiting. The enrollment target is 200 participants. The study started on 2018-02-13. Estimated completion is 2030-06.
What conditions does trial NCT03695978 study?
This clinical trial studies the following conditions: Haemophilia A. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
Who is sponsoring clinical trial NCT03695978?
This trial is sponsored by Octapharma, which has 73 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03695978 being conducted?
This trial has 20 study locations across Florida, Louisiana, Nevada, Ontario. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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