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NCT02145234 · ClinicalTrials.gov registry record · Phase 1

Placebo-Controlled, Single and Multiple Ascending Subcutaneous Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986089 in Healthy Adult Subjects

A Phase 1 study of Healthy Adults, sponsored by Hoffmann-La Roche.

Completed
Registry status
Phase 1
Development phase
140
Enrollment target
1
Study location

NCT02145234 is a Phase 1 study of Healthy Adults that has completed, run by Hoffmann-La Roche. The registered enrollment target is 140 participants, above the 82-participant average among 33 other Healthy Adults trials with a reported enrollment target (71% higher). The trial reports 1 study location across 1 state.

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The verdict

NCT02145234, a Phase 1 study of Healthy Adults, has completed, sponsored by Hoffmann-La Roche.

COMPLETED
Registry status
Phase 1
Development phase
140 participants
Enrollment target
1
Study location

Study Summary

The purpose of this study is to evaluate the safety, tolerability, immunogenicity, pharmacokinetics and pharmacodynamics of single and multiple doses of BMS-986089 in healthy adult subjects.

Conditions Studied

Interventions

  • DRUG BMS-986089
  • DRUG Placebo matching with BMS-986089

Study Locations (1)

California

  • Wcct Global, Llc - Cypress

Trial Details

FieldValue
Enrollment Target 140 participants
Start Date 2014-06-30
Est. Completion 2016-02-29
Phase Phase 1

Sponsor

Hoffmann-La Roche

909 total trials

What the Registry Record Tells You About NCT02145234

The ClinicalTrials.gov registry entry for NCT02145234 describes a study currently listed as completed, categorized as Phase 1. The registered enrollment target is 140 participants, a figure that helps gauge the scale of data the investigators plan to collect, above the 82-participant average among 33 other Healthy Adults trials with a reported enrollment target (71% higher). The listed sponsor is Hoffmann-La Roche, which has 909 total studies on file at ClinicalTrials.gov.

The record links to 1 condition, with Healthy Adults appearing as the primary indexed condition, and to 2 interventions - of which BMS-986089 is the first listed.

NCT02145234 reports 1 study location spanning 1 distinct geographic area - top geographies include California.

Frequently Asked Questions

What is clinical trial NCT02145234 about?

NCT02145234 is a clinical study titled "Placebo-Controlled, Single and Multiple Ascending Subcutaneous Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of BMS-986089 in Healthy Adult Subjects". The purpose of this study is to evaluate the safety, tolerability, immunogenicity, pharmacokinetics and pharmacodynamics of single and multiple doses of BMS-986089 in healthy adult subjects.

What is the current status of trial NCT02145234?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 140 participants. The study started on 2014-06-30. Estimated completion is 2016-02-29.

What conditions does trial NCT02145234 study?

This clinical trial studies the following conditions: Healthy Adults.

What interventions are being tested in trial NCT02145234?

The interventions under investigation include: BMS-986089 (DRUG), Placebo matching with BMS-986089 (DRUG).

Who is sponsoring clinical trial NCT02145234?

This trial is sponsored by Hoffmann-La Roche, which has 909 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT02145234 being conducted?

This trial has 1 study location across California. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

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

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.