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A Study to Assess the Pharmacokinetics, Safety and Tolerability of Single-dose Adagrasib (BMS-986503) in Healthy Participants of Japanese Descent

A Study to Assess the Pharmacokinetics, Safety and Tolerability of Single-dose Adagrasib (BMS-986503) in Healthy Participants of Japanese Descent

Recruiting
18-60 years
All
Phase 1

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Overview

The aim of this study is to assess the pharmacokinetics, safety and tolerability of single-dose Adagrasib (BMS-986503) in healthy participants of Japanese descent

Eligibility

Inclusion Criteria:

  • Participants must be of Japanese descent (both biological parents of the participant are ethnically Japanese).
  • Participants must be healthy adult without clinically significant deviation from normal in medical history, PE, 12-lead ECG, vital sign measurements, and clinical laboratory assessments as determined by the investigator.
  • Participants must have Body mass index of 18.0 kg/m2 to 32.0 kg/m2.
  • Participants must have Total body weight ≥ 50 kg.

Exclusion Criteria:

  • Participants must not have significant history or clinical manifestation of any metabolic, allergic, dermatological, renal, hematological, pulmonary, cardiovascular, gastrointestinal, neurological, respiratory, endocrine, or psychiatric disorder, as determined by the investigator.
  • Other protocol defined Inclusion/Exclusion criteria apply.

Study details
    Healthy Participants

NCT07723118

Mirati Therapeutics Inc.

29 August 2026

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