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Gene Therapy for Haemophilia A.
NCT03001830 · View on ClinicalTrials.gov ↗
Study Summary
The GO-8 study focuses on assessing safety and efficacy of gene therapy for patients with severe haemophilia A
Conditions Studied
Interventions
- BIOLOGICAL AAV2/8-HLP-FVIII-V3
Study Locations (4)
Idaho
- St. Luke'S Regional Medical Center, Ltd — Boise
Kentucky
- University of Kentucky — Lexington
Tennessee
- St Jude's Children's Research Hospital — Memphis
Other
- Royal Free Hospital — London
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 14 participants |
| Start Date | 2017-06-14 |
| Est. Completion | 2029-12 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT03001830
The ClinicalTrials.gov registry entry for NCT03001830 describes a study currently listed as active not recruiting. It is categorized as Phase 1, 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 14 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is University College, London, which has 6 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 Hemophilia A appearing as the primary indexed condition, and to 1 intervention — of which AAV2/8-HLP-FVIII-V3 is the first listed. 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: NCT03001830 reports 4 study locations spanning 4 distinct geographic areas — top geographies include Idaho, Kentucky, Tennessee. 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 NCT03001830 about?
NCT03001830 is a clinical study titled "Gene Therapy for Haemophilia A.". The GO-8 study focuses on assessing safety and efficacy of gene therapy for patients with severe haemophilia A
What is the current status of trial NCT03001830?
This trial is currently active not recruiting. It is a Phase 1 study. The enrollment target is 14 participants. The study started on 2017-06-14. Estimated completion is 2029-12.
What conditions does trial NCT03001830 study?
This clinical trial studies the following conditions: Hemophilia A. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT03001830?
The interventions under investigation include: AAV2/8-HLP-FVIII-V3 (BIOLOGICAL). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT03001830?
This trial is sponsored by University College, London, which has 6 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT03001830 being conducted?
This trial has 4 study locations across Idaho, Kentucky, Tennessee. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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