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NCT02500706 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of Faster-acting Insulin Aspart Compared to NovoRapid® Both in Combination With Insulin Degludec in Adults With Type 1 Diabetes

A Phase 3 study of Diabetes and Diabetes Mellitus, Type 1, sponsored by Novo Nordisk A/S.

Completed
Registry status
Phase 3
Development phase
1,108
Enrollment target
20
Study locations

NCT02500706: Completed Phase 3 study of Diabetes and Diabetes Mellitus, Type 1, sponsored by Novo Nordisk A/S.

NCT02500706 is a Phase 3 study of Diabetes and Diabetes Mellitus, Type 1 that has completed, run by Novo Nordisk A/S. The registered enrollment target is 1,108 participants, below the 3,025-participant average among 338 other Diabetes trials with a reported enrollment target (63% lower). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT02500706, a Phase 3 study of Diabetes and Diabetes Mellitus, Type 1, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 3
Development phase
1,108 participants
Enrollment target
20
Study locations

Study Summary

This trial is conducted in Asia, Europe and North America. The purpose is to confirm efficacy in terms of glycaemic control of treatment with mealtime faster-acting insulin aspart in combination with insulin degludec in adults with Type 1 Diabetes Mellitus.

Primary Outcome

Change from baseline (week 0) in HbA1c was evaluated after 26 weeks of randomisation. The results are based on the last in-trial value, which included the last available measurement in the in-trial period. In-trial period: the observation period from date of randomisation until last trial-related subject-site contact.

Interventions

  • DRUG insulin aspart
  • DRUG Faster-acting insulin aspart
  • DRUG insulin degludec

Study Locations (20)

California

  • Novo Nordisk Investigational Site - Concord
  • Novo Nordisk Investigational Site - Encino
  • Novo Nordisk Investigational Site - Escondido
  • Novo Nordisk Investigational Site - Fresno
  • Novo Nordisk Investigational Site - Fullerton
  • Novo Nordisk Investigational Site - Huntington Beach
  • Novo Nordisk Investigational Site - Monterey
  • Novo Nordisk Investigational Site - Newport Beach
  • Novo Nordisk Investigational Site - Santa Barbara
  • Novo Nordisk Investigational Site - Walnut Creek

Colorado

  • Novo Nordisk Investigational Site - Denver
  • Novo Nordisk Investigational Site - Golden

Florida

  • Novo Nordisk Investigational Site - Palm Harbor
  • Novo Nordisk Investigational Site - Tampa

Kentucky

  • Novo Nordisk Investigational Site - Lexington
  • Novo Nordisk Investigational Site - Louisville

Arizona

  • Novo Nordisk Investigational Site - Tucson

Georgia

  • Novo Nordisk Investigational Site - Roswell

Idaho

  • Novo Nordisk Investigational Site - Idaho Falls

Kansas

  • Novo Nordisk Investigational Site - Topeka

Trial Details

FieldValue
Enrollment Target 1,108 participants
Start Date 2016-05-04
Est. Completion 2017-08-16
Phase Phase 3
Novo Nordisk A/S

431 total trials

What the finished NCT02500706 record still lists

NCT02500706 is an interventional study that assigns participants to a tested intervention. Its 1,108 participants enrollment target places it among the larger protocols in the corpus, below the 3,025-participant average among 338 other Diabetes trials with a reported enrollment target (63% lower).

The record links to 2 conditions, with Diabetes appearing as the primary indexed condition, and to 3 interventions - of which insulin aspart is the first listed.

NCT02500706 names 20 study sites across 8 states, led by California, Colorado, Florida.

Frequently Asked Questions

What is clinical trial NCT02500706 about?

NCT02500706 is a clinical study titled "Efficacy and Safety of Faster-acting Insulin Aspart Compared to NovoRapid® Both in Combination With Insulin Degludec in Adults With Type 1 Diabetes". This trial is conducted in Asia, Europe and North America. The purpose is to confirm efficacy in terms of glycaemic control of treatment with mealtime faster-acting insulin aspart in combination with insulin degludec in adults with Type 1 Diabetes Mellitus.

What is the current status of trial NCT02500706?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,108 participants. The study started on 2016-05-04. Estimated completion is 2017-08-16.

What conditions does trial NCT02500706 study?

This clinical trial studies the following conditions: Diabetes, Diabetes Mellitus, Type 1.

What interventions are being tested in trial NCT02500706?

The interventions under investigation include: insulin aspart (DRUG), Faster-acting insulin aspart (DRUG), insulin degludec (DRUG).

Who is sponsoring clinical trial NCT02500706?

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

Where is trial NCT02500706 being conducted?

This trial has 20 study locations across Arizona, California, Colorado, Florida, Georgia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Diabetes

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 NCT02500706's enrollment target sits among peer trials

1,108 40th of 338 higher than 299 of 338 other Diabetes trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Diabetes 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 NCT02500706, the US trial registry maintained by the National Library of Medicine. NCT02500706 (large enrollment · wide site footprint · completed) retrieved and formatted by PlainTrial, see methodology.