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NCT02971969 · ClinicalTrials.gov registry record

Long-Term Safety, Tolerability, and Efficacy of DTX101 (AAVrh10FIX) in Adults With Moderate/Severe to Severe Hemophilia B

A clinical trial of Hemophilia B, sponsored by Ultragenyx Pharmaceutical.

Completed
Registry status
6
Enrollment target
5
Study locations

NCT02971969: Completed study of Hemophilia B, sponsored by Ultragenyx Pharmaceutical.

NCT02971969 is a study of Hemophilia B that has completed, run by Ultragenyx Pharmaceutical. The registered enrollment target is 6 participants, below the 96-participant average among 20 other Hemophilia B trials with a reported enrollment target (94% lower). The trial reports 5 study locations across 5 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02971969, a study of Hemophilia B, has completed, sponsored by Ultragenyx Pharmaceutical.

COMPLETED
Registry status
6 participants
Enrollment target
5
Study locations

Study Summary

A long-term follow-up study to evaluate the safety, tolerability, and efficacy of DTX101 in adult males with moderate/severe to severe hemophilia B.

Conditions Studied

Study Locations (5)

Arkansas

  • Arkansas Children's Hospital - Little Rock

Florida

  • UF CRC - Clinical Research Center - Gainesville

Michigan

  • University of Michigan Hospital and Health Systems - Ann Arbor

Hampshire

  • Haemophilia, Haemostasis & Thrombosis Centre - Basingstoke

Other

  • Manchester Haemophilia Comprehensive Care Center - Manchester

Trial Details

FieldValue
Enrollment Target 6 participants
Start Date 2017-01
Est. Completion 2021-11-06
Ultragenyx Pharmaceutical

52 total trials

What the finished NCT02971969 record still lists

NCT02971969 is an observational study that tracks outcomes without assigning an intervention. The registry caps enrollment at 6 participants, a relatively small participant target, below the 96-participant average among 20 other Hemophilia B trials with a reported enrollment target (94% lower).

The record links to 1 condition, with Hemophilia B appearing as the primary indexed condition, and to 0 interventions.

NCT02971969 lists 5 locations in 5 states (Arkansas, Florida, Michigan).

Frequently Asked Questions

What is clinical trial NCT02971969 about?

NCT02971969 is a clinical study titled "Long-Term Safety, Tolerability, and Efficacy of DTX101 (AAVrh10FIX) in Adults With Moderate/Severe to Severe Hemophilia B". A long-term follow-up study to evaluate the safety, tolerability, and efficacy of DTX101 in adult males with moderate/severe to severe hemophilia B.

What is the current status of trial NCT02971969?

This trial is currently completed. The enrollment target is 6 participants. The study started on 2017-01. Estimated completion is 2021-11-06.

What conditions does trial NCT02971969 study?

This clinical trial studies the following conditions: Hemophilia B.

Who is sponsoring clinical trial NCT02971969?

This trial is sponsored by Ultragenyx Pharmaceutical, which has 52 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02971969 being conducted?

This trial has 5 study locations across Arkansas, Florida, Michigan, Hampshire. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Hemophilia B

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT02971969's enrollment target sits among peer trials

6 21st of 20 the lowest of 20 other Hemophilia B trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Hemophilia B trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT02971969, the US trial registry maintained by the National Library of Medicine. NCT02971969 (small enrollment · multi site footprint · completed) retrieved and formatted by PlainTrial, see methodology.