RecruitingPhase 1NCT07628881

A Study to Investigate the Relative Bioavailability and Food Effect of Tablet for Oral Suspension of Sonrotoclax in Healthy Adults

A Phase 1, Single-dose, Open-label, Randomized, Crossover Study in Healthy Adult Participants to Evaluate Relative Bioavailability and Food Effect of Tablet for Oral Suspension of Sonrotoclax


Sponsor

BeOne Medicines

Enrollment

12 participants

Start Date

Jun 17, 2026

Study Type

INTERVENTIONAL

Conditions

Summary

The purpose of this study is to evaluate whether blood levels of sonrotoclax after administration of a tablet for oral suspension are similar to those observed with the current sonrotoclax tablet. In addition, this study evaluates the effect of food on the absorption of sonrotoclax after administration of the tablet for oral suspension and the resulting blood levels of sonrotoclax.


Eligibility

Min Age: 18 YearsMax Age: 60 Years

Plain Language Summary

Simplified for easier understanding

This clinical trial is studying a drug called Sonrotoclax Tablet and a drug called Sonrotoclax Tablet for Oral Suspension for people with healthy volunteers. The study is currently recruiting participants at 1 location. People eligible for this study include aged 18 Years to 60 Years.

This summary was AI-generated to explain the trial in plain language. It is not medical advice. Always discuss eligibility with your doctor before enrolling in a clinical trial.

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Interventions

DRUGSonrotoclax Tablet for Oral Suspension

Administered orally

DRUGSonrotoclax Tablet

Administered orally


Locations(1)

Linear Early Phase

Joondalup, Western Australia, Australia

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NCT07628881


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