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Completed Phase 1 Interventional Accepts healthy volunteers

Bioequivalence of a Zanubrutinib Tablet Compared to Capsules in Healthy Adult Participants

ClinicalTrials.gov ID: NCT05767398

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This page only displays public information reproduced from the official ClinicalTrials.gov record NCT05767398. It adds no medical advice, opinions, or eligibility judgments. The official record remains the source of truth for eligibility criteria, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Nov 12, 2026, 9:07 AM EST

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Official title

A Single-dose, Open-label, Randomized, Replicate Crossover Study in Healthy Adult Subjects to Assess the Bioequivalence of a Zanubrutinib Tablet Compared to Zanubrutinib Capsules

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

Study to determine the bioequivalence of a zanubrutinib tablet compared to capsules in healthy adult participants.

Study identification

NCT ID
NCT05767398
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1
Lead sponsor
BeiGene
Industry
Enrollment
58 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years to 65 Years
Sex
All
Healthy volunteers
Accepts healthy volunteers

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Mar 7, 2023 (Actual)
Primary completion
Apr 28, 2023 (Actual)
Completion
Apr 28, 2023 (Actual)
Last update posted
Oct 26, 2024

2023

United States locations

U.S. sites
1
U.S. states
1
U.S. cities
1
Facility City State ZIP Site status
Fortrea Clinical Research Unit Dallas Texas 75247 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05767398, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Oct 26, 2024 · Synced Nov 12, 2026

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