Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT02849080 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation Versus Sitagliptin in Subjects With Type 2 Diabetes Mellitus.

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

Completed
Registry status
Phase 3
Development phase
504
Enrollment target

NCT02849080: Completed Phase 3 study, sponsored by Novo Nordisk A/S.

NCT02849080 is a Phase 3 study that has completed, run by Novo Nordisk A/S. The registered enrollment target is 504 participants, below the 772-participant average among 15,282 other Phase 3 trials with a reported enrollment target (35% lower). According to ClinicalTrials.gov, the official US trial registry.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT02849080, a Phase 3 study, has completed, sponsored by Novo Nordisk A/S.

COMPLETED
Registry status
Phase 3
Development phase
504 participants
Enrollment target

Study Summary

This trial is globally conducted. The aim of this trial is to investigate Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation versus Sitagliptin in Subjects with Type 2 Diabetes Mellitus.

Primary Outcome

Participants who achieved HbA1c \<7.0% (American Diabetes Association (ADA) target) (yes/no), was evaluated at week 52. The endpoint was evaluated based on the data from the in-trial observation period, which was the time period from when a participant was randomised until the final scheduled visit, including any period after initiation of rescue medication and/or premature discontinuation of trial product. The endpoint was also evaluated based on the data from the on-treatment without rescue me

Interventions

  • DRUG semaglutide
  • DRUG sitagliptin

Trial Details

FieldValue
Enrollment Target 504 participants
Start Date 2016-09-20
Est. Completion 2019-03-27
Phase Phase 3
Novo Nordisk A/S

431 total trials

What the finished NCT02849080 record still lists

NCT02849080 is an interventional study that assigns participants to a tested intervention. The registered 504 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 (35% lower).

The record links to 0 conditions, and to 2 interventions - of which semaglutide is the first listed.

NCT02849080 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT02849080 about?

NCT02849080 is a clinical study titled "Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation Versus Sitagliptin in Subjects With Type 2 Diabetes Mellitus.". This trial is globally conducted. The aim of this trial is to investigate Efficacy and Safety of Oral Semaglutide Using a Flexible Dose Adjustment Based on Clinical Evaluation versus Sitagliptin in Subjects with Type 2 Diabetes Mellitus.

What is the current status of trial NCT02849080?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 504 participants. The study started on 2016-09-20. Estimated completion is 2019-03-27.

What interventions are being tested in trial NCT02849080?

The interventions under investigation include: semaglutide (DRUG), sitagliptin (DRUG).

Who is sponsoring clinical trial NCT02849080?

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 NCT02849080's enrollment target sits among peer trials

504 742nd of 2000 higher than 1,258 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

Nationwide trials with similar profiles

Cross-condition peers matched on enrollment target and registry start date, not the same-condition list above.

Similar enrollment target

  • NCT05846282 · 504 participants · NA

    Students Rising Above: Offsetting the Health and Mental Health Costs of Resilience

  • NCT06072131 · 504 participants · Phase 3

    To Evaluate Efficacy of Belinostat or Pralatrexate in Combination Against CHOP Alone in PTCL

  • NCT06736522 · 504 participants · NA

    Future Leaders Program: Testing a Youth Leadership, Engagement, and Mindfulness Program

  • NCT06822257 · 504 participants · NA

    Drinking in Young Adult Duos (DYAD) Study

Similar registry start date

  • NCT05962346 · started 2026-12 · NA

    Fetal Endoscopic Tracheal Occlusion for Congenital Diaphragmatic Hernia

  • NCT07125183 · started 2026-12 · Phase 2

    Study on Efficacy and Tolerability of Weekly Doxorubicin in Elderly Patients With Advanced or Metastatic Leiomyosarcoma

  • NCT07292298 · started 2026-11 · Phase 2

    Phase 2 Single-Arm Rectal Cancer Brachytherapy for Patients With Low-Lying Residual Adenocarcinoma After Total Neoadjuvant Therapy to Improve Organ Preservation Rates

  • NCT04263285 · started 2026-10 · NA

    Treatment of Depression Post-SCI

Source: ClinicalTrials.gov NCT02849080, the US trial registry maintained by the National Library of Medicine. NCT02849080 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.