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NCT02229851 · ClinicalTrials.gov registry record · Phase 3

Trial to Compare the Efficacy and Safety of NNC0195-0092 (Somapacitan) With Placebo and Norditropin® FlexPro® (Somatropin) in Adults With Growth Hormone Deficiency.

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

Completed
Registry status
Phase 3
Development phase
301
Enrollment target

NCT02229851: Completed Phase 3 study, sponsored by Novo Nordisk A/S.

NCT02229851 is a Phase 3 study that has completed, run by Novo Nordisk A/S. The registered enrollment target is 301 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (61% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02229851, a Phase 3 study, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 3
Development phase
301 participants
Enrollment target

Study Summary

This study is conducted globally. The purpose is to demonstrate the efficacy of once weekly dosing of NNC0195-0092 (somapacitan) compared to placebo and once-daily dosing of somatropin (human growth hormone, hGH) after 35 weeks of treatment in adults with growth hormone deficiency.

Primary Outcome

Change in Truncal fat percentage was measured from baseline (week -3) until the end of the main treatment period (week 34).

Interventions

  • DRUG placebo
  • DRUG somatropin
  • DRUG somapacitan

Trial Details

FieldValue
Enrollment Target 301 participants
Start Date 2014-10-31
Est. Completion 2018-05-07
Phase Phase 3
Novo Nordisk A/S

431 total trials

What the finished NCT02229851 record still lists

NCT02229851 is an interventional study that assigns participants to a tested intervention. The registered 301 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 (61% lower).

The record links to 0 conditions, and to 3 interventions - of which placebo is the first listed.

NCT02229851 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02229851 about?

NCT02229851 is a clinical study titled "Trial to Compare the Efficacy and Safety of NNC0195-0092 (Somapacitan) With Placebo and Norditropin® FlexPro® (Somatropin) in Adults With Growth Hormone Deficiency.". This study is conducted globally. The purpose is to demonstrate the efficacy of once weekly dosing of NNC0195-0092 (somapacitan) compared to placebo and once-daily dosing of somatropin (human growth hormone, hGH) after 35 weeks of treatment in adults with growth hormone deficiency.

What is the current status of trial NCT02229851?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 301 participants. The study started on 2014-10-31. Estimated completion is 2018-05-07.

What interventions are being tested in trial NCT02229851?

The interventions under investigation include: placebo (DRUG), somatropin (DRUG), somapacitan (DRUG).

Who is sponsoring clinical trial NCT02229851?

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 NCT02229851's enrollment target sits among peer trials

301 1121st of 2000 higher than 879 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 NCT02229851, the US trial registry maintained by the National Library of Medicine. NCT02229851 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.