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NCT02137850 · ClinicalTrials.gov registry record · Phase 3

Safety and Efficacy of Turoctocog Alfa Pegol (N8-GP) in Previously Untreated Patients With Haemophilia A

A Phase 3 study, sponsored by Novo Nordisk A/S.

Completed
Registry status
Phase 3
Development phase
124
Enrollment target

NCT02137850: Completed Phase 3 study, sponsored by Novo Nordisk A/S.

NCT02137850 is a Phase 3 study that has completed, run by Novo Nordisk A/S. The registered enrollment target is 124 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02137850, a Phase 3 study, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 3
Development phase
124 participants
Enrollment target

Study Summary

This trial is conducted globally. The aim of the trial is to investigate the safety and efficacy of turoctocog alfa pegol (N8-GP) in previously untreated patients (PUPs) with haemophilia A.

Primary Outcome

Number of participants with inhibitory antibodies against coagulation factor VIII (FVIII) was reported during the main and extension phase of the trial.

Interventions

  • DRUG turoctocog alfa pegol

Trial Details

FieldValue
Enrollment Target 124 participants
Start Date 2014-06-26
Est. Completion 2023-06-07
Phase Phase 3
Novo Nordisk A/S

431 total trials

What the finished NCT02137850 record still lists

NCT02137850 is an interventional study that assigns participants to a tested intervention. The registered 124 participants enrollment target is mid-sized for trials with a published cap, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (84% lower).

The record links to 0 conditions, and to 1 intervention - of which turoctocog alfa pegol is the first listed.

NCT02137850 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02137850 about?

NCT02137850 is a clinical study titled "Safety and Efficacy of Turoctocog Alfa Pegol (N8-GP) in Previously Untreated Patients With Haemophilia A". This trial is conducted globally. The aim of the trial is to investigate the safety and efficacy of turoctocog alfa pegol (N8-GP) in previously untreated patients (PUPs) with haemophilia A.

What is the current status of trial NCT02137850?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 124 participants. The study started on 2014-06-26. Estimated completion is 2023-06-07.

What interventions are being tested in trial NCT02137850?

The interventions under investigation include: turoctocog alfa pegol (DRUG).

Who is sponsoring clinical trial NCT02137850?

This trial is sponsored by Novo Nordisk A/S, which has 431 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT02137850's enrollment target sits among peer trials

124 1610th of 2000 higher than 386 of 2,000 other Phase 3 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 3 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 NCT02137850, the US trial registry maintained by the National Library of Medicine. NCT02137850 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.