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Search / Trial NCT05638282

A Study to Evaluate the Safety and Tolerability of Cendakimab in Chinese Healthy Participants

Launched by BRISTOL-MYERS SQUIBB · Nov 30, 2022

Trial Information

Current as of January 14, 2025

Completed

Keywords

Healthy Chinese Cendakimab

ClinConnect Summary

No description provided

Gender

ALL

Eligibility criteria

  • Inclusion Criteria:
  • Participants must be Chinese (both biological parents are ethnically Chinese).
  • Body mass index (BMI) of 18.0 through 28.0 kilograms/meter squared (kg/m\^2), inclusive. BMI = weight (kg)/\[height (m)\]\^2.
  • Body weight ≥ 50.0 kg.
  • Exclusion Criteria:
  • History of clinically significant infection within 4 weeks of dosing on Day 1.
  • Significant medical history/condition, laboratory abnormality, or psychiatric illness that would prevent the participant from participating in the study.
  • Condition(s) which may confound the ability to interpret data from the study, as determined by the investigator.
  • Other protocol-defined inclusion/exclusion criteria apply.

Trial Officials

Bristol-Myers Squibb

Study Director

Bristol-Myers Squibb

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

Guangzhou, Guangdong, China

People applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

Discussion 0

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