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NCT05494762 · ClinicalTrials.gov registry record · Phase 1
Safety, Pharmacokinetics, and Antitumor Activity of BGB-B167 Alone and in Combination With Tislelizumab (BGB-A317) in Participants With Advanced Solid Tumors
A Phase 1 study, sponsored by BeiGene.
- Terminated
- Registry status
- Phase 1
- Development phase
- 55
- Enrollment target
NCT05494762: Clinical Trial Phase 1 study, sponsored by BeiGene.
NCT05494762 is a Phase 1 study that was terminated before completion, run by BeiGene. The registered enrollment target is 55 participants, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target. According to ClinicalTrials.gov, the official US trial registry.
The verdict
NCT05494762, a Phase 1 study, was terminated before completion, sponsored by BeiGene.
- TERMINATED
- Registry status
- Phase 1
- Development phase
- 55 participants
- Enrollment target
Study Summary
This study will evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of BGB-B167 monotherapy and in combination with tislelizumab (BGB-A317) in participants with select advanced solid tumors.
Interventions
- DRUG Tislelizumab
- DRUG BGB-B167
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 55 participants |
| Start Date | 2022-08-25 |
| Est. Completion | 2025-02-24 |
| Phase | Phase 1 |
Why NCT05494762 stopped before completion
NCT05494762 is an interventional study that assigns participants to a tested intervention. The registry caps enrollment at 55 participants, a relatively small participant target, roughly in line with the 60-participant average among 29,502 other Phase 1 trials with a reported enrollment target.
The record links to 0 conditions, and to 2 interventions - of which Tislelizumab is the first listed.
NCT05494762 does not publish any study locations in the registry export this page uses.
Frequently Asked Questions
What is clinical trial NCT05494762 about?
NCT05494762 is a clinical study titled "Safety, Pharmacokinetics, and Antitumor Activity of BGB-B167 Alone and in Combination With Tislelizumab (BGB-A317) in Participants With Advanced Solid Tumors". This study will evaluate the safety, tolerability, pharmacokinetics (PK), and preliminary antitumor activity of BGB-B167 monotherapy and in combination with tislelizumab (BGB-A317) in participants with select advanced solid tumors.
What is the current status of trial NCT05494762?
This trial is currently terminated. It is a Phase 1 study. The enrollment target is 55 participants. The study started on 2022-08-25. Estimated completion is 2025-02-24.
What interventions are being tested in trial NCT05494762?
The interventions under investigation include: Tislelizumab (DRUG), BGB-B167 (DRUG).
Who is sponsoring clinical trial NCT05494762?
This trial is sponsored by BeiGene, which has 65 total clinical trials registered on ClinicalTrials.gov.
Learn More About Clinical Trials
How this trial's enrollment target compares
Where NCT05494762's enrollment target sits among peer trials
55 918th of 2000 higher than 1,070 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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