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NCT01605994 · ClinicalTrials.gov registry record · Phase 1

Multiple Ascending-Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-933043 in Healthy Subjects

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

Completed
Registry status
Phase 1
Development phase
115
Enrollment target

NCT01605994 is a Phase 1 study that has completed, run by Bristol-Myers Squibb. The registered enrollment target is 115 participants.

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The verdict

NCT01605994, a Phase 1 study, has completed, sponsored by Bristol-Myers Squibb.

COMPLETED
Registry status
Phase 1
Development phase
115 participants
Enrollment target

Study Summary

Includes a placebo-controlled sequential, ascending multiple-dose panels (10 panels, 8 ascending doses, and 2 fixed Japanese Panels exploring safety, tolerability, and Pharmacokinetic (PK) measures

Interventions

  • DRUG BMS-933043
  • DRUG Placebo matching with BMS-933043
  • DRUG Antacid Buffer Predose Solution

Trial Details

FieldValue
Enrollment Target 115 participants
Start Date 2012-07
Est. Completion 2013-12
Phase Phase 1

Sponsor

Bristol-Myers Squibb

1,025 total trials

What the Registry Record Tells You About NCT01605994

The ClinicalTrials.gov registry entry for NCT01605994 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 115 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 3 interventions - of which BMS-933043 is the first listed.

NCT01605994 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT01605994 about?

NCT01605994 is a clinical study titled "Multiple Ascending-Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics of BMS-933043 in Healthy Subjects". Includes a placebo-controlled sequential, ascending multiple-dose panels (10 panels, 8 ascending doses, and 2 fixed Japanese Panels exploring safety, tolerability, and Pharmacokinetic (PK) measures

What is the current status of trial NCT01605994?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 115 participants. The study started on 2012-07. Estimated completion is 2013-12.

What interventions are being tested in trial NCT01605994?

The interventions under investigation include: BMS-933043 (DRUG), Placebo matching with BMS-933043 (DRUG), Antacid Buffer Predose Solution (DRUG).

Who is sponsoring clinical trial NCT01605994?

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.