A Study of BMS-986195 in Healthy Male Subjects

NCT03245515 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 24

Last updated 2018-01-05

No results posted yet for this study

Summary

The purpose of this study is to investigate the effects BMS-986195 in healthy male subjects.

Conditions

Interventions

DRUG

BMS-986195

specified dose on specified days

Sponsors & Collaborators

Principal Investigators

  • Bristol-Myers Squibb · Bristol-Myers Squibb

Study Design

Allocation
NA
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

Min Age
18 Years
Max Age
55 Years
Sex
MALE
Healthy Volunteers
Yes

Timeline & Regulatory

Start
2017-08-15
Primary Completion
2017-09-22
Completion
2017-10-05
FDA Drug
Yes

Countries

  • Netherlands

Study Locations

More Related Trials

Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT03245515 on ClinicalTrials.gov