Can a cancer drug be tailored for japanese patients? a new trial seeks answers
NCT ID NCT07723118
First seen Jul 23, 2026 · Last updated Aug 25, 2026 · Updated 3 times
Summary
This early-stage study is testing how a single dose of the experimental cancer drug adagrasib is processed by the body in 10 healthy adults of Japanese descent. Researchers will measure drug levels in the blood and monitor for any side effects. The goal is to gather safety and pharmacokinetic data to guide future studies in Japanese patients.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- a single dose of the experimental cancer drug adagrasib (BMS-986503)
- What this could lead to
- If successful, this study could help determine the right dosing of adagrasib for Japanese patients in future trials.
- What could go wrong
- This is a very early, small study in only 10 healthy people, so results may not predict effects in patients or broader populations.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1
The first testing in people. Mainly checks safety and dose, usually in a small group.
- Participants
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About 10 people
The number the study aims to enrol. It can still change while the study runs.
- Started
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Aug 2026
- Expected to finish
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Sep 2026
An estimate. End dates often move.
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 to 60 years
- Sex
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Anyone
- Healthy volunteers
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Accepted
You do not need to have the condition being studied to take part.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
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.
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As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
How to take part
Only the study team decides who joins. These are the ways to reach them.
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The places running it
1 site. The list below names each one and where it is.
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The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
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A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
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CenExel ACT (Formerly Anaheim Clinical Trials; LLC)
RECRUITINGAnaheim, California, 92801, United States
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