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NCT01240980 · ClinicalTrials.gov registry record · Phase 1

Safety Study of BMS-903452 in Healthy Subjects (Panel 1-7) & Relative Bioavailability of the Crystalline and Amorphous Forms of BMS-903452 [Panels 4, 6, 11 & 12(Part A)], and Subjects With Type 2 Diabetes Mellitus (Part B)

A Phase 1 study, sponsored by Bristol-Myers Squibb.

Completed
Registry status
Phase 1
Development phase
104
Enrollment target

NCT01240980 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 104 participants.

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The verdict

NCT01240980, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
104 participants
Enrollment target

Study Summary

The purpose of this study is to evaluate the safety, tolerability and effect on blood glucose control of BMS-903452 compared to placebo in healthy subjects \& relative bioavailability of the crystalline and amorphous forms of BMS-903452 \[Panels 4,6,11 \& 12(Part A)\] ; and subjects with type 2 Diabetes Mellitus (Part B). The study will also determine the amount of BMS-903452 in the blood.

Interventions

  • DRUG BMS-903452

Trial Details

FieldValue
Enrollment Target 104 participants
Start Date 2010-11
Est. Completion 2012-01
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT01240980

The ClinicalTrials.gov registry entry for NCT01240980 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 104 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Bristol-Myers Squibb, which has 1,025 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 1 intervention - of which BMS-903452 is the first listed.

NCT01240980 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01240980 about?

NCT01240980 is a clinical study titled "Safety Study of BMS-903452 in Healthy Subjects (Panel 1-7) & Relative Bioavailability of the Crystalline and Amorphous Forms of BMS-903452 [Panels 4, 6, 11 & 12(Part A)], and Subjects With Type 2 Diabetes Mellitus (Part B)". The purpose of this study is to evaluate the safety, tolerability and effect on blood glucose control of BMS-903452 compared to placebo in healthy subjects \& relative bioavailability of the crystalline and amorphous forms of BMS-903452 \[Panels 4,6,11 \& 12(Part A)\] ; and subjects with type 2 Diab...

What is the current status of trial NCT01240980?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 104 participants. The study started on 2010-11. Estimated completion is 2012-01.

What interventions are being tested in trial NCT01240980?

The interventions under investigation include: BMS-903452 (DRUG).

Who is sponsoring clinical trial NCT01240980?

This trial is sponsored by Bristol-Myers Squibb, which has 1,025 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.