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NCT01414920 · ClinicalTrials.gov registry record · Phase 2

Efficacy and Safety of TAK-875 in Combination With Sitagliptin in Participants With Type 2 Diabetes Mellitus

A Phase 2 study, sponsored by Takeda.

Completed
Registry status
Phase 2
Development phase
368
Enrollment target

NCT01414920: Completed Phase 2 study, sponsored by Takeda.

NCT01414920 is a Phase 2 study that has completed, run by Takeda. The registered enrollment target is 368 participants, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (177% higher). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT01414920, a Phase 2 study, has completed, sponsored by Takeda.

COMPLETED
Registry status
Phase 2
Development phase
368 participants
Enrollment target

Study Summary

The purpose of this study is to determine the efficacy and safety of TAK-875, once daily (QD), in combination with sitagliptin QD in participants with type 2 diabetes mellitus (T2DM).

Primary Outcome

The change in the value of glycosylated hemoglobin (the concentration of glucose bound to hemoglobin as a percent of the absolute maximum that can be bound) collected at week 12 relative to baseline.

Interventions

  • DRUG Placebo
  • DRUG Sitagliptin
  • DRUG TAK-875
  • DRUG TAK-875 and Sitagliptin

Trial Details

FieldValue
Enrollment Target 368 participants
Start Date 2011-08
Est. Completion 2012-08
Phase Phase 2
Takeda

408 total trials

What the finished NCT01414920 record still lists

NCT01414920 is an interventional study that assigns participants to a tested intervention. The registered 368 participants enrollment target is mid-sized for trials with a published cap, above the 133-participant average among 30,622 other Phase 2 trials with a reported enrollment target (177% higher).

The record links to 0 conditions, and to 4 interventions - of which Placebo is the first listed.

NCT01414920 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT01414920 about?

NCT01414920 is a clinical study titled "Efficacy and Safety of TAK-875 in Combination With Sitagliptin in Participants With Type 2 Diabetes Mellitus". The purpose of this study is to determine the efficacy and safety of TAK-875, once daily (QD), in combination with sitagliptin QD in participants with type 2 diabetes mellitus (T2DM).

What is the current status of trial NCT01414920?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 368 participants. The study started on 2011-08. Estimated completion is 2012-08.

What interventions are being tested in trial NCT01414920?

The interventions under investigation include: Placebo (DRUG), Sitagliptin (DRUG), TAK-875 (DRUG), TAK-875 and Sitagliptin (DRUG).

Who is sponsoring clinical trial NCT01414920?

This trial is sponsored by Takeda, which has 408 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT01414920's enrollment target sits among peer trials

368 121st of 2000 higher than 1,880 of 2,000 other Phase 2 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 2 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 NCT01414920, the US trial registry maintained by the National Library of Medicine. NCT01414920 (mid enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.