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NCT01205724 · ClinicalTrials.gov registry record · Phase 1

Safety and Pharmacokinetics of NNC 0129-0000-1003 in Subjects With Haemophilia A

A Phase 1 study, sponsored by Novo Nordisk A/S.

Completed
Registry status
Phase 1
Development phase
27
Enrollment target

NCT01205724: Completed Phase 1 study, sponsored by Novo Nordisk A/S.

NCT01205724 is a Phase 1 study that has completed, run by Novo Nordisk A/S. The registered enrollment target is 27 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01205724, a Phase 1 study, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 1
Development phase
27 participants
Enrollment target

Study Summary

This trial is conducted globally. The aim of this clinical trial is to investigate the safety and pharmacokinetics (the determination of the concentration of the administered medication in blood over time) of NNC 0129-0000-1003 in previously treated subjects with severe haemophilia A.

Interventions

  • DRUG turoctocog alfa pegol

Trial Details

FieldValue
Enrollment Target 27 participants
Start Date 2010-09
Est. Completion 2011-04
Phase Phase 1
Novo Nordisk A/S

431 total trials

What the finished NCT01205724 record still lists

NCT01205724 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 27 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (55% lower).

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

NCT01205724 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01205724 about?

NCT01205724 is a clinical study titled "Safety and Pharmacokinetics of NNC 0129-0000-1003 in Subjects With Haemophilia A". This trial is conducted globally. The aim of this clinical trial is to investigate the safety and pharmacokinetics (the determination of the concentration of the administered medication in blood over time) of NNC 0129-0000-1003 in previously treated subjects with severe haemophilia A.

What is the current status of trial NCT01205724?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 27 participants. The study started on 2010-09. Estimated completion is 2011-04.

What interventions are being tested in trial NCT01205724?

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

Who is sponsoring clinical trial NCT01205724?

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 NCT01205724's enrollment target sits among peer trials

27 1463rd of 2000 higher than 519 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 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 NCT01205724, the US trial registry maintained by the National Library of Medicine. NCT01205724 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.