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Search / Trial NCT06084598

A Study to Evaluate the Safety, Tolerability and Drug Levels of BMS-986446 in Healthy Participants and Healthy Participants of Japanese Ethnicity

Launched by BRISTOL-MYERS SQUIBB · Oct 10, 2023

Trial Information

Current as of April 29, 2025

Completed

Keywords

Pharmacokinetics Healthy Participants Healthy Japanese Participants Bms 986446 Prx005

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participant must be of Japanese ethnicity (both biological parents are ethnically Japanese) for Part 1 and Part 2, Panel 2. No limitations on ethnicity apply to Part 2, Panel 1
  • Participant is healthy, without any significant abnormalities in medical history, physical examination, ECGs, or clinical laboratory assessments determinations, as assessed by the investigator
  • Body mass index (BMI) of at least 18 kg/m\^2 but no more than 32 kg/m\^2 at screening
  • Body weight between 45 kg and 110 kg
  • Exclusion Criteria:
  • Any clinically significant deviation from normal, as judged by the investigator
  • Any major surgery within 90 days of study drug administration
  • Participation in another interventional clinical trial concurrent with this study
  • Note: Other protocol-defined inclusion/exclusion criteria apply

About Bristol Myers Squibb

Bristol-Myers Squibb (BMS) is a global biopharmaceutical company dedicated to discovering, developing, and delivering innovative medicines that help patients prevail over serious diseases. With a robust portfolio of products across multiple therapeutic areas, including oncology, immunology, cardiovascular, and fibrotic diseases, BMS emphasizes cutting-edge research and a commitment to advancing medical science through clinical trials. The company is driven by a mission to provide transformative therapies, leveraging collaboration and scientific expertise to address unmet medical needs and improve patient outcomes worldwide.

Locations

Cypress, California, United States

Cypress, California, United States

Patients applied

0 patients applied

Trial Officials

Bristol-Myers Squibb

Study Director

Bristol-Myers Squibb

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported