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Cohort J2 for Healthy Subjects

Phase 1
Waitlist Available
Research Sponsored by Bristol-Myers Squibb
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial
Must have
Be between 18 and 65 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up up to day 92
Awards & highlights

Study Summary

This trial tests a new drug to see how safe and effective it is in healthy Japanese people.

Timeline

Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~up to day 92
This trial's timeline: 3 weeks for screening, Varies for treatment, and up to day 92 for reporting.

Treatment Details

Study Objectives

Outcome measures can provide a clearer picture of what you can expect from a treatment.
Primary outcome measures
Number of participants with Adverse events
Number of participants with ECG abnormalities
Number of participants with clinical laboratory abnormalities
+2 more
Secondary outcome measures
Absolute Bioavailability (F) of BMS-986325
Area under the serum concentration-time curve from time zero to time of last quantifiable concentration (AUC(0-T))
Maximum observed serum concentration (Cmax)
+4 more

Trial Design

3Treatment groups
Experimental Treatment
Group I: Cohort J3Experimental Treatment2 Interventions
Group II: Cohort J2Experimental Treatment2 Interventions
Group III: Cohort J1Experimental Treatment2 Interventions
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Placebo
1995
Completed Phase 3
~2670
BMS-986325
2023
Completed Phase 1
~30

Find a Location

Logistics

Participation is compensated

You will be compensated for participating in this trial.

Who is running the clinical trial?

Bristol-Myers SquibbLead Sponsor
2,638 Previous Clinical Trials
4,128,489 Total Patients Enrolled

Media Library

BMS-986325 (Other) Clinical Trial Eligibility Overview. Trial Name: NCT05813717 — Phase 1
Healthy Subjects Research Study Groups: Cohort J2, Cohort J3, Cohort J1
Healthy Subjects Clinical Trial 2023: BMS-986325 Highlights & Side Effects. Trial Name: NCT05813717 — Phase 1
BMS-986325 (Other) 2023 Treatment Timeline for Medical Study. Trial Name: NCT05813717 — Phase 1

Frequently Asked Questions

These questions and answers are submitted by anonymous patients, and have not been verified by our internal team.

Has Cohort J1 obtained authorization from the FDA?

"Cohort J1's safety score is 1 as it is currently in Phase 1, meaning there are only limited clinical data supporting its efficacy and safety."

Answered by AI

Is this experiment currently enrolling participants?

"Clinicaltrials.gov confirms that this trial is actively recruiting participants, beginning April 10th 2023 and being updated most recently on May 2nd of the same year."

Answered by AI

Does this trial accept patients of advanced age?

"Eligibility for this research is contingent on the candidate's age, being over 18 and younger than 50."

Answered by AI

Who is able to participate in this clinical research?

"In order to be considered for this medical experiment, applicants need to have a clean bill of health and fall within the 18-50 year old demographic. The trial will accept up to 24 volunteers in total."

Answered by AI

What is the size of this trial's cohort?

"Affirmative. According to records on clinicaltrials.gov, this clinical trial is currently soliciting participants and was first posted on April 10th 2023. The last update occurred on May 2nd 2023; the project requires 24 people from two sites for full enrollment."

Answered by AI
Recent research and studies
clinicaltrials.govStudy
A Study to Evaluate the Safety, Tolerability, Drug Levels, and Drug Effects of BMS-986325 in Healthy Japanese Participants
2023. "A Study to Evaluate the Safety, Tolerability, Drug Levels, and Drug Effects of BMS-986325 in Healthy Japanese Participants". ClinicalTrials.gov. https://clinicaltrials.gov/ct2/show/NCT05813717.
~12 spots leftby Apr 2025
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