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NCT06776679 · ClinicalTrials.gov registry record · Phase 1

A Study of How [14C]-BGB-16673 is Absorbed, Broken Down, and Removed From the Body After a Single Oral Dose in Healthy Participants

A Phase 1 study, sponsored by BeiGene.

Completed
Registry status
Phase 1
Development phase
8
Enrollment target

NCT06776679: Completed Phase 1 study, sponsored by BeiGene.

NCT06776679 is a Phase 1 study that has completed, run by BeiGene. The registered enrollment target is 8 participants, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower). According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06776679, a Phase 1 study, has completed, sponsored by BeiGene.

COMPLETED
Registry status
Phase 1
Development phase
8 participants
Enrollment target

Study Summary

The purpose of this study is to determine the absorption, metabolism, and excretion of \[14C\]-BGB-16673 and to characterize and determine, where possible, the metabolites present in plasma, urine, and feces in healthy male participants following a single oral administration.

Interventions

  • DRUG [14C]-BGB-16673

Trial Details

FieldValue
Enrollment Target 8 participants
Start Date 2025-01-24
Est. Completion 2025-03-27
Phase Phase 1
BeiGene

65 total trials

What the finished NCT06776679 record still lists

NCT06776679 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 8 participants, a relatively small participant target, below the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target (87% lower).

The record links to 0 conditions, and to 1 intervention - of which [14C]-BGB-16673 is the first listed.

NCT06776679 does not publish any study locations in the registry export this page uses.

Frequently Asked Questions

What is clinical trial NCT06776679 about?

NCT06776679 is a clinical study titled "A Study of How [14C]-BGB-16673 is Absorbed, Broken Down, and Removed From the Body After a Single Oral Dose in Healthy Participants". The purpose of this study is to determine the absorption, metabolism, and excretion of \[14C\]-BGB-16673 and to characterize and determine, where possible, the metabolites present in plasma, urine, and feces in healthy male participants following a single oral administration.

What is the current status of trial NCT06776679?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 8 participants. The study started on 2025-01-24. Estimated completion is 2025-03-27.

What interventions are being tested in trial NCT06776679?

The interventions under investigation include: [14C]-BGB-16673 (DRUG).

Who is sponsoring clinical trial NCT06776679?

This trial is sponsored by BeiGene, which has 65 total clinical trials registered on ClinicalTrials.gov.

How this trial's enrollment target compares

Where NCT06776679's enrollment target sits among peer trials

8 1959th of 2000 higher than 29 of 2,000 other Phase 1 trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Phase 1 trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06776679, the US trial registry maintained by the National Library of Medicine. NCT06776679 (small enrollment · none site footprint · completed) retrieved and formatted by PlainTrial, see methodology.